Genomes and Genes
Alias: Zea mays, Zea mays L., Zea mays mays, Zea mays var. japonica
Publications332 found, 100 shown here
- Rare genetic variation at Zea mays crtRB1 increases beta-carotene in maize grainJianbing Yan
International Maize and Wheat Improvement Center, Texcoco, Mexico
Nat Genet 42:322-7. 2010..Experimental evidence from association and linkage populations in maize (Zea mays L...
- A genomic and expression compendium of the expanded PEBP gene family from maizeOlga N Danilevskaya
Pioneer Hi Bred International Inc, A DuPont Business, Johnston, IA 50131, USA
Plant Physiol 146:250-64. 2008..Twenty-five maize (Zea mays) genes that encode PEBP-like proteins, likely the entire gene family, were identified and named Zea mays ..
- The regulatory c1 locus of Zea mays encodes a protein with homology to myb proto-oncogene products and with structural similarities to transcriptional activatorsJ Paz-Ares
Max Planck Institut fur Zuchtungsforschung, Koln, FRG
EMBO J 6:3553-8. 1987The structure of the wild-type c1 locus of Zea mays was determined by sequence analysis of one genomic and two cDNA clones...
- Maize Mu transposons are targeted to the 5' untranslated region of the gl8 gene and sequences flanking Mu target-site duplications exhibit nonrandom nucleotide composition throughout the genomeCharles R Dietrich
Interdepartmental Plant Physiology Program, Iowa State University, Ames, Iowa 50011, USA
Genetics 160:697-716. 2002The widespread use of the maize Mutator (Mu) system to generate mutants exploits the preference of Mu transposons to insert into genic regions. However, little is known about the specificity of Mu insertions within genes...
- Structure and expression of the maize (Zea mays L.) SUN-domain protein gene family: evidence for the existence of two divergent classes of SUN proteins in plantsShaun P Murphy
Institute of Molecular Biophysics, The Florida State University, Tallahassee, FL 32306 4370, USA
BMC Plant Biol 10:269. 2010....
- Alternatively spliced products of the maize P gene encode proteins with homology to the DNA-binding domain of myb-like transcription factorsE Grotewold
Cold Spring Harbor Laboratory, NY 11724
Proc Natl Acad Sci U S A 88:4587-91. 1991The Zea mays P gene has been postulated to regulate the biosynthetic pathway of a flavonoid-derived pigment in certain floral tissues [Styles, E. D. & Ceska, O. (1977) Can. J. Genet. Cytol. 19, 289-302]...
- Genetic control of abscisic acid biosynthesis in maizeB C Tan
Plant Molecular and Cellular Biology Graduate Program, Horticultural Sciences Department, 2237 Fifield Hall, University of Florida, Gainesville, FL 32611, USA
Proc Natl Acad Sci U S A 94:12235-40. 1997..The viviparous seed mutants of maize identify genes involved in synthesis and perception of ABA...
- Characterization of maize (Zea mays L.) Wee1 and its activity in developing endospermY Sun
Department of Plant Sciences, University of Arizona, Tucson, AZ 85721, USA
Proc Natl Acad Sci U S A 96:4180-5. 1999We report the characterization of a maize Wee1 homologue and its expression in developing endosperm. Using a 0.8-kb cDNA from an expressed sequence tag project, we isolated a 1...
- ZmMKK4, a novel group C mitogen-activated protein kinase kinase in maize (Zea mays), confers salt and cold tolerance in transgenic ArabidopsisXiangpei Kong
State Key Laboratory of Crop Biology, Shandong Key Laboratory of Crop Biology, College of Life Sciences, Shandong Agricultural University, Tai an 271018, Shandong, China
Plant Cell Environ 34:1291-303. 2011..In this study, we isolated a novel group C MAPKK gene, ZmMKK4, from maize. Northern blotting analysis revealed that the ZmMKK4 transcript expression was up-regulated by cold, high salt and ..
- A maize CONSTANS-like gene, conz1, exhibits distinct diurnal expression patterns in varied photoperiodsTheresa A Miller
Department of Biological Sciences, Marquette University, Milwaukee, WI 53201 1881, USA
Planta 227:1377-88. 2008Maize (Zea mays ssp. mays L.) was domesticated from teosinte (Z. mays L. ssp. parviglumis Iltis & Doebley), a plant requiring short day photoperiods to flower...
- Structure of linkage disequilibrium and phenotypic associations in the maize genomeD L Remington
Department of Genetics, North Carolina State University, Raleigh, NC 27695 7614, USA
Proc Natl Acad Sci U S A 98:11479-84. 2001..We report patterns of local and genome-wide LD in 102 maize inbred lines representing much of the worldwide genetic diversity used in maize breeding, and address its ..
- Timing and biosynthetic potential for carotenoid accumulation in genetically diverse germplasm of maizeRatnakar Vallabhaneni
Department of Biological Sciences, Lehman College, City University of New York, Bronx, New York 10468, USA
Plant Physiol 150:562-72. 2009..The grass family (Poaceae) contains major crop staples, including maize (Zea mays), wheat (Triticum aestivum), rice (Oryza sativa), sorghum (Sorghum bicolor), and millet (Pennisetum glaucum)...
- Maize Brittle stalk2 encodes a COBRA-like protein expressed in early organ development but required for tissue flexibility at maturityAnoop Sindhu
Department of Botany and Plant Pathology, Purdue University, West Lafayette, Indiana 47907 2054, USA
Plant Physiol 145:1444-59. 2007The maize (Zea mays) brittle stalk2 (bk2) is a recessive mutant, the aerial parts of which are easily broken. The bk2 phenotype is developmentally regulated and appears 4 weeks after planting, at about the fifth-leaf stage...
- The Relationship between auxin transport and maize branchingAndrea Gallavotti
Cold Spring Harbor Laboratory, Cold Spring Harbor, New York 11724, USA
Plant Physiol 147:1913-23. 2008Maize (Zea mays) plants make different types of vegetative or reproductive branches during development. Branches develop from axillary meristems produced on the flanks of the vegetative or inflorescence shoot apical meristem...
- Involvement of the MADS-box gene ZMM4 in floral induction and inflorescence development in maizeOlga N Danilevskaya
Pioneer Hi Bred International, Inc, A DuPont Company, Johnston, Iowa 50131, USA
Plant Physiol 147:2054-69. 2008..the molecular determinants involved in this process, we performed genome-wide RNA expression profiling on maize (Zea mays) shoot apices at vegetative and early reproductive stages using massively parallel signature sequencing ..
- A wound-responsive and phospholipid-regulated maize calcium-dependent protein kinaseJadwiga Szczegielniak
Institute of Biochemistry and Biophysics, Polish Academy of Sciences, 02 106 Warsaw, Poland
Plant Physiol 139:1970-83. 2005..Using protein sequence data obtained from a calcium- and phospholipid-regulated protein kinase purified from maize (Zea mays), we isolated a cDNA encoding a calcium-dependent protein kinase (CDPK), which we designated ZmCPK11...
- Complete cDNA and genomic sequence encoding a flooding-responsive gene from maize (Zea mays L.) homologous to xyloglucan endotransglycosylaseI N Saab
Department of Agronomy, University of Illinois at Urbana Champaign 61801, USA
Plant Physiol 108:439-40. 1995
- Cloning of two cDNAs encoding calnexin-like and calreticulin-like proteins from maize (Zea mays) leaves: identification of potential calcium-binding domainsB A Kwiatkowski
Institute of Biochemistry and Biophysics, Polish Academy of Sciences, Warsaw, Poland
Gene 165:219-22. 1995..cDNAs encoding calnexin (Cln)-like and calreticulin (Crl)-like proteins have been isolated by immunoscreening of a maize leaf cDNA library...
- Expression of cell wall related genes in basal and ear internodes of silking brown-midrib-3, caffeic acid O-methyltransferase (COMT) down-regulated, and normal maize plantsSabine Guillaumie
INRA, Unité de Génétique et d Amélioration des Plantes Fourragères, BP6, F 86600 Lusignan, France
BMC Plant Biol 8:71. 2008Silage maize is a major forage and energy resource for cattle feeding, and several studies have shown that lignin content and structure are the determining factors in forage maize feeding value...
- CRS1 is a novel group II intron splicing factor that was derived from a domain of ancient originB Till
Institute of Molecular Biology, University of Oregon, Eugene 97403, USA
RNA 7:1227-38. 2001..The maize nuclear gene crs1 is required for the splicing of the group II intron in the chloroplast atpF gene...
- Molecular characterization of Na+/H+ antiporters (ZmNHX) of maize (Zea mays L.) and their expression under salt stressChristian Zörb
Interdisciplinary Research Center, Institute of Plant Nutrition, Justus Liebig University, Heinrich Buff Ring 26 32, Giessen D 35392, Germany
J Plant Physiol 162:55-66. 2005Six full-length gene transcripts ZmNHX1-6 from Zea mays L. that were homologous to tonoplast-associated Na+/H+ antiporter were identified...
- Regulation and functional analysis of ZmDREB2A in response to drought and heat stresses in Zea mays LFeng Qin
Biological Resources Division, Japan International Research Center for Agricultural Sciences JIRCAS, 1 1 Ohwashi, Tsukuba, Ibaraki 305 8686, Japan
Plant J 50:54-69. 2007..In this research, we report the cloning of a DREB2 homolog from maize, ZmDREB2A, whose transcripts were accumulated by cold, dehydration, salt and heat stresses in maize seedlings...
- Significant improvement of stress tolerance in tobacco plants by overexpressing a stress-responsive aldehyde dehydrogenase gene from maize (Zea mays)Weizao Huang
Ministry of Education Key Laboratory for Southwest Bio resource and Ecoenvironment, College of Life Science and State Key Laboratory of Hydraulics and Mountain River Engineering, Sichuan University, Chengdu 610064, China
Plant Mol Biol 68:451-63. 2008..In order to identify genes required for the stresses responses in the grass crop Zea mays, an ALDH (ZmALDH22A1) gene was isolated and characterized...
- Two CRM protein subfamilies cooperate in the splicing of group IIB introns in chloroplastsYukari Asakura
Institute of Molecular Biology, University of Oregon, Eugene, OR 97403, USA
RNA 14:2319-32. 2008....
- Over-expression of a Zea mays L. protein phosphatase 2C gene (ZmPP2C) in Arabidopsis thaliana decreases tolerance to salt and droughtLixia Liu
State Key Laboratory of Crop Biology, College of Life Sciences, Shandong Agricultural University, Tai an, Shandong, PR China
J Plant Physiol 166:531-42. 2009ZmPP2C (AY621066) is a protein phosphatase type-2c previously isolated from roots of Zea mays (LD9002)...
- Expression and functional characterization of two pathogenesis-related protein 10 genes from Zea maysYu Rong Xie
Department of Plant Pathology and Crop Physiology, 302 Life Sciences Building, Louisiana State University Agricultural Center, Baton Rouge, LA 70803, USA
J Plant Physiol 167:121-30. 2010A novel PR10 gene (ZmPR10.1) was isolated from maize and its expression and function were compared with the previous ZmPR10. ZmPR10.1 shares 89.8% and 85.7% identity to ZmPR10 at the nucleotide and amino acid sequence level, respectively...
- Characterization of a cinnamoyl-CoA reductase 1 (CCR1) mutant in maize: effects on lignification, fibre development, and global gene expressionBarek Tamasloukht
Laboratoire de Recherche en Sciences Végétales, Pôle de Biotechnologies Végétales, Castanet Tolosan, France
J Exp Bot 62:3837-48. 2011..By screening a Mu insertional mutant collection in maize, a mutant in the CCR1 gene was isolated named Zmccr1(-)...
- ZCN8 encodes a potential orthologue of Arabidopsis FT florigen that integrates both endogenous and photoperiod flowering signals in maizeChloë M Lazakis
Department of Molecular and Cellular Biology, University of Guelph, Guelph, Ontario, Canada N1G 2W1
J Exp Bot 62:4833-42. 2011..Recently, a large family of FT homologues in maize, the Zea CENTRORADIALIS (ZCN) genes, was described, suggesting that maize also contains FT-related proteins that ..
- Binding of ABI4 to a CACCG motif mediates the ABA-induced expression of the ZmSSI gene in maize (Zea mays L.) endospermYu Feng Hu
College of Agronomy, Sichuan Agricultural University, Chengdu, Sichuan, 611130, China
J Exp Bot 63:5979-89. 2012Starch synthase I (SSI) contributes the majority of the starch synthase activity in developing maize endosperm...
- Characterization of AMT-mediated high-affinity ammonium uptake in roots of maize (Zea mays L.)Riliang Gu
Department of Plant Nutrition, Key Laboratory of Plant Soil Interactions, MOE, Center for Resources, Environment and Food Security, China Agricultural University, Beijing 100193, China
Plant Cell Physiol 54:1515-24. 2013..In this study we aimed at characterizing AMT-mediated ammonium transport in maize, for which ammonium-based fertilizer is an important nitrogen (N) source...
- Comparative molecular and biochemical characterization of segmentally duplicated 9-lipoxygenase genes ZmLOX4 and ZmLOX5 of maizeYong Soon Park
Department of Plant Pathology and Microbiology, Texas A and M University, College Station, TX 77843 2132, USA
Planta 231:1425-37. 2010..Herein we report on molecular and biochemical characterization of two closely related maize 9-lipoxygenase paralogs, ZmLOX4 and ZmLOX5...
- Maize calcium-dependent protein kinase (ZmCPK11): local and systemic response to wounding, regulation by touch and components of jasmonate signalingJadwiga Szczegielniak
Institute of Biochemistry and Biophysics, Polish Academy of Sciences, Pawinskiego 5A, 02 106 Warsaw, Poland
Physiol Plant 146:1-14. 2012Expression of ZmCPK11, a member of the maize (Zea mays) calcium-dependent protein kinases (CDPKs) family, is induced by mechanical wounding. A rapid increase of the activity of a 56-kDa CDPK has been observed in damaged leaves...
- A genome-wide regulatory framework identifies maize pericarp color1 controlled genesKengo Morohashi
Department of Molecular Genetics, The Ohio State University, Columbus, OH 43210, USA
Plant Cell 24:2745-64. 2012..P1) encodes an R2R3-MYB transcription factor responsible for the accumulation of insecticidal flavones in maize (Zea mays) silks and red phlobaphene pigments in pericarps and other floral tissues, which makes P1 an important visual ..
- The duplicated chalcone synthase genes C2 and Whp (white pollen) of Zea mays are independently regulated; evidence for translational control of Whp expression by the anthocyanin intensifying gene inP Franken
Max Planck Institut fur Zuchtungsforschung, Köln 30, FRG
EMBO J 10:2605-12. 1991Two chalcone synthase genes in maize have been cloned and molecularly characterized to be the C2 and the Whp (white pollen) locus...
- Characterization of an immunoglobulin binding protein homolog in the maize floury-2 endosperm mutantE B Fontes
Department of Botany, North Carolina State University, Raleigh 27695 7612
Plant Cell 3:483-96. 1991The maize b-70 protein is an endoplasmic reticulum protein overproduced in the floury-2 (fl2) endosperm mutant. The increase in b-70 levels in fl2 plants occurs during seed maturation and is endosperm specific...
- The Viviparous-1 developmental gene of maize encodes a novel transcriptional activatorD R McCarty
Vegetable Crops Department, University of Florida, Gainesville 32611
Cell 66:895-905. 1991The Viviparous-1 (Vp1) gene of maize is specifically required for expression of the maturation program in seed development. We show that Vp1 encodes a 73,335 dalton protein with no detectable homology to known proteins...
- Purification and characterization of phospholipase D (PLD) from rice (Oryza sativa L.) and cloning of cDNA for PLD from rice and maize (Zea mays L.)J Ueki
Japan Tobacco Inc, Plant Breeding and Genetics Research Laboratory, Shizuoka
Plant Cell Physiol 36:903-14. 1995..A cDNA for PLD was also isolated from maize. The similarity of the deduced amino acid sequences of PLD was 90% between rice and maize, 73% between the cereals ..
- Close split of sorghum and maize genome progenitorsZuzana Swigonova
Waksman Institute of Microbiology, Rutgers University, Piscataway, New Jersey 08854, USA
Genome Res 14:1916-23. 2004It is generally believed that maize (Zea mays L. ssp. mays) arose as a tetraploid; however, the two progenitor genomes cannot be unequivocally traced within the genome of modern maize...
- Enzymes that control the thiamine diphosphate pool in plant tissues. Properties of thiamine pyrophosphokinase and thiamine-(di)phosphate phosphatase purified from Zea mays seedlingsMaria Rapala-Kozik
Faculty of Biochemistry, Biophysics and Biotechnology, Jagiellonian University, Gronostajowa 7, 30 387 Krakow, Poland
Plant Physiol Biochem 47:237-42. 2009..In this work, we characterize highly purified preparations of TPK and a TDP/TMP phosphatase isolated from 6-day Zea mays seedlings. TPK was the 29-kDa monomeric protein, with the optimal activity at pH 9.0, the K(m) values of 12...
- The HD-ZIP IV transcription factor OCL4 is necessary for trichome patterning and anther development in maizeVanessa Vernoud
Universite de Lyon, Ecole Normale Superieure de Lyon, Université Lyon1, IFR128 Biosciences Lyon Gerland, Unité Reproduction et Développement des Plantes, F 69364 Lyon, France
Plant J 59:883-94. 2009..Here, we report the functional analysis of the maize HD-ZIP IV gene OCL4 (outer cell layer 4) via the phenotypic analysis of two insertional mutants, and of OCL4-RNAi ..
- Nucleotide diversity and molecular evolution of the PSY1 gene in Zea mays compared to some other grass speciesZhiyuan Fu
National Maize Improvement Center of China, Key Laboratory of Crop Genomics and Genetic Improvement, China Agricultural University, Yuanmingyuan West Road, Haidian, Beijing, China
Theor Appl Genet 120:709-20. 2010..diversity and evolution pattern of PSY1 within the Andropogoneae, sequences of 76 accessions from 5 species (maize, teosinte, tripsacum, coix, and sorghum) of the Andropogoneae were tested, along with 4 accessions of rice (Oryza ..
- Functional analysis of maize RAD51 in meiosis and double-strand break repairJin Li
Department of Genetics, Development and Cell Biology, Iowa State Unversity, Ames, Iowa 50011, USA
Genetics 176:1469-82. 2007..Double mutants of the two Zea mays L...
- Maize AMEIOTIC1 is essential for multiple early meiotic processes and likely required for the initiation of meiosisWojciech P Pawlowski
Department of Plant Breeding and Genetics, Cornell University, Ithaca, NY 14853, USA
Proc Natl Acad Sci U S A 106:3603-8. 2009..gene, which affects the transition to meiosis and progression through the early stages of meiotic prophase in maize. We demonstrate that all meiotic processes require am1, including expression of meiosis-specific genes, ..
- barren inflorescence2 Encodes a co-ortholog of the PINOID serine/threonine kinase and is required for organogenesis during inflorescence and vegetative development in maizePaula McSteen
Department of Biology, Pennsylvania State University, University Park, Pennsylvania 16802, USA
Plant Physiol 144:1000-11. 2007..Maize (Zea mays) and rice (Oryza sativa) have additional types of axillary meristems in the inflorescence compared to Arabidopsis ..
- The evolution of apical dominance in maizeJ Doebley
Department of Plant Biology, University of Minnesota, St Paul 55108, USA
Nature 386:485-8. 1997..A striking example of this phenomenon is seen in maize (Zea mays spp...
- Maize floral regulator protein INDETERMINATE1 is localized to developing leaves and is not altered by light or the sink/source transitionAda Y M Wong
Department of Molecular and Cellular Biology, University of Guelph, Guelph, Ontario, Canada N1G 2W1
J Exp Bot 58:403-14. 2007..encodes a putative transcription factor that plays an important role in regulating the transition to flowering in maize. Mutant id1 plants have a prolonged vegetative growth phase and fail to make normal flowers...
- Genetic and physical interaction suggest that BARREN STALK 1 is a target of BARREN INFLORESCENCE2 in maize inflorescence developmentAndrea Skirpan
Department of Biology, The Pennsylvania State University, University Park, PA 16802, USA
Plant J 55:787-97. 2008Organogenesis in plants is controlled by polar auxin transport. In maize (Zea mays), barren inflorescence2 (bif2) encodes a co-ortholog of the serine/threonine protein kinase PINOID (PID), which regulates auxin transport in Arabidopsis...
- Isolation and characterization of cDNA clones encoding a functional p34cdc2 homologue from Zea maysJ Colasanti
Cold Spring Harbor Laboratory, NY 11724
Proc Natl Acad Sci U S A 88:3377-81. 1991We describe the isolation of cDNA clones encoding a p34cdc2 homologue from a higher plant, Zea mays (maize). A full-length cDNA clone, cdc2ZmA, was isolated, sequenced, and shown to complement a cdc28 mutation in Saccharomyces cerevisiae...
- Contrasting effects of selection on sequence diversity and linkage disequilibrium at two phytoene synthase lociKelly A Palaisa
Department of Plant and Soil Sciences, University of Delaware, and Delaware Biotechnology Institute, Newark, DE 19716, USA
Plant Cell 15:1795-806. 2003..the effects of human selection for yellow endosperm color, representing increased carotenoid content, on two maize genes, the Y1 phytoene synthase and PSY2, a putative second phytoene synthase...
- A CRM domain protein functions dually in group I and group II intron splicing in land plant chloroplastsYukari Asakura
Institute of Molecular Biology, University of Oregon, Eugene, Oregon 97403, USA
Plant Cell 19:3864-75. 2007..RNA coimmunoprecipitation assays showed that CFM2 in maize (Zea mays) chloroplasts is associated with the group I intron in pre-trnL-UAA and group II introns in the ndhA and ycf3 pre-..
- A phenylalanine in DGAT is a key determinant of oil content and composition in maizePeizhong Zheng
Pioneer Hi Bred International Inc, A DuPont Company, 7300 NW 62nd Avenue, PO Box 1004, Johnston, Iowa 50131, USA
Nat Genet 40:367-72. 2008..Here we show that a high-oil QTL (qHO6) affecting maize seed oil and oleic-acid contents encodes an acyl-CoA:diacylglycerol acyltransferase (DGAT1-2), which catalyzes the ..
- Expression of ADP-glucose pyrophosphorylase in maize (Zea mays L.) grain and source leaf during grain fillingJ L Prioul
Institut de Recherche sur les Plantes, Associé au Centre National de la Recherche Scientifique Unité Recherche Associée 1128, Universite de Paris Sud, Orsay, France
Plant Physiol 104:179-87. 1994..pyrophosphorylase activity and of starch accumulation rate measured in grain, from pollination to maturity, in Zea mays L. plants grown outdoors, was coincident for 2 years...
- Molecular characterization of cytokinin-responsive histidine kinases in maize. Differential ligand preferences and response to cis-zeatinKeiko Yonekura-Sakakibara
Plant Science Center, RIKEN, 1 7 22, Suehiro, Tsurumi, Yokohama 230 0045, Japan
Plant Physiol 134:1654-61. 2004Genes for cytokinin-responsive His-protein kinases (ZmHK1, ZmHK2, and ZmHK3a) were isolated from maize (Zea mays)...
- Genomic analysis of the 12-oxo-phytodienoic acid reductase gene family of Zea maysJinglan Zhang
Department of Plant Pathology and Microbiology, Department of Plant Pathology, Texas A and M University, 2132 TAMU, College Station, TX 77843 2132, USA
Plant Mol Biol 59:323-43. 2005..and analysis of ESTs and genomic sequences from available private and public databases revealed that the maize genome encodes eight OPR genes...
- Proteome and phosphoproteome analysis of starch granule-associated proteins from normal maize and mutants affected in starch biosynthesisFlorent Grimaud
Institut National de la Recherche Agronomique, Unité de Recherche Biopolymères, Interactions, Assemblages, BP 71627, F 44316 Nantes Cedex 03, France
J Exp Bot 59:3395-406. 2008..immunological, and proteomic approaches to investigate comprehensively the proteome and phosphoproteome of Zea mays endosperm starch granules...
- Sugar levels regulate tryptophan-dependent auxin biosynthesis in developing maize kernelsSherry LeClere
United States Department of Agriculture Agricultural Research Service, Center for Medical, Agricultural, and Veterinary Entomology, Chemistry Unit, Gainesville, Florida 32608 1069, USA
Plant Physiol 153:306-18. 2010The maize (Zea mays) Miniature1 (Mn1) locus encodes the cell wall invertase INCW2, which is localized predominantly in the basal endosperm transfer layer of developing kernels and catalyzes the conversion of sucrose into glucose and ..
- Maize opaque endosperm mutations create extensive changes in patterns of gene expressionBrenda G Hunter
Department of Plant Sciences, University of Arizona, Tucson, AZ 85721, USA
Plant Cell 14:2591-612. 2002b>Maize starchy endosperm mutants have kernel phenotypes that include a brittle texture, susceptibility to insect pests, and inferior functional characteristics of products made from their flour...
- Characterization of dull1, a maize gene coding for a novel starch synthaseM Gao
Department of Biochemistry and Biophysics, Iowa State University, Ames, Iowa 50011, USA
Plant Cell 10:399-412. 1998The maize dull1 (du1) gene is a determinant of the structure of endosperm starch, and du1- mutations affect the activity of two enzymes involved in starch biosynthesis, starch synthase II (SSII) and starch branching enzyme IIa (SBEIIa)...
- ZmYS1 functions as a proton-coupled symporter for phytosiderophore- and nicotianamine-chelated metalsGabriel Schaaf
Institut für Pflanzenernährung, Universitat Hohenheim, D 70593 Stuttgart, Germany
J Biol Chem 279:9091-6. 2004..Despite its physiological importance at alkaline pH, uptake of Fe-phytosiderophores into roots of wild-type maize plants was greater at acidic pH and sensitive to the proton uncoupler CCCP...
- The CRM domain: an RNA binding module derived from an ancient ribosome-associated proteinAlice Barkan
Institute of Molecular Biology, University of Oregon, Eugene, Oregon 97403 1229, USA
RNA 13:55-64. 2007..GFP fused to a single-domain CRM protein from maize localizes to the nucleolus, suggesting that an analogous activity may have been retained in plants...
- Maize regulatory gene opaque-2 encodes a protein with a "leucine-zipper" motif that binds to zein DNAR J Schmidt
Department of Biology, University of California, San Diego, La Jolla 92093
Proc Natl Acad Sci U S A 87:46-50. 1990The opaque-2 locus (o2) in maize regulates the expression of many members of the zein multigene family of storage proteins...
- OHP1: a maize basic domain/leucine zipper protein that interacts with opaque2L D Pysh
Department of Biology, University of California, San Diego, La Jolla 92093 0116
Plant Cell 5:227-36. 1993..Whole genome DNA gel blot analysis of maize recombinant inbreds revealed two strongly hybridizing restriction fragments, neither of which mapped close to any ..
- The maize INDETERMINATE1 flowering time regulator defines a highly conserved zinc finger protein family in higher plantsJoseph Colasanti
Department of Molecular and Cellular Biology, University of Guelph, Guelph, Ontario, N1G 2W1, Canada
BMC Genomics 7:158. 2006The maize INDETERMINATE1 gene, ID1, is a key regulator of the transition to flowering and the founding member of a transcription factor gene family that encodes a protein with a distinct arrangement of zinc finger motifs...
- Expression differences between normal and indeterminate1 maize suggest downstream targets of ID1, a floral transition regulator in maizeViktoriya Coneva
Department of Molecular and Cellular Biology, University of Guelph, Guelph, Ontario, Canada
J Exp Bot 58:3679-93. 2007The INDETERMINATE1 (ID1) transcription factor is a key regulator of the transition to flowering in maize. ID1 is expressed in immature leaves where it controls the production or transmission of leaf-derived florigenic signals...
- Miniature1-encoded cell wall invertase is essential for assembly and function of wall-in-growth in the maize endosperm transfer cellByung Ho Kang
Department of Microbiology, University of Florida, Gainesville, Florida 32611, USA
Plant Physiol 151:1366-76. 2009The miniature1 (mn1) seed phenotype in maize (Zea mays) is due to a loss-of-function mutation at the Mn1 locus that encodes a cell wall invertase (INCW2) that localizes exclusively to the basal endosperm transfer cells (BETCs) of ..
- A pentatricopeptide repeat protein facilitates the trans-splicing of the maize chloroplast rps12 pre-mRNAChristian Schmitz-Linneweber
Institute of Molecular Biology, University of Oregon, Eugene, Oregon 97403, USA
Plant Cell 18:2650-63. 2006..To gain insight into the functions and substrates of the PPR protein family, we characterized the maize (Zea mays) nuclear gene ppr4, which encodes a chloroplast-targeted protein harboring both a PPR tract and an RNA ..
- BARREN INFLORESCENCE2 interaction with ZmPIN1a suggests a role in auxin transport during maize inflorescence developmentAndrea Skirpan
Department of Biology, The Pennsylvania State University, 208 Mueller Lab, University Park, PA 16802, USA
Plant Cell Physiol 50:652-7. 2009..In maize, BARREN INFLORESCENCE2 (BIF2) encodes a serine/threonine protein kinase co-orthologous to PINOID (PID), which ..
- The En/Spm transposable element of Zea mays contains splice sites at the termini generating a novel intron from a dSpm element in the A2 geneA Menssen
Max Planck Institut fur Zuchtungsforschung, Molekulare Pflanzengenetik, Koln, FRG
EMBO J 9:3051-7. 1990The A2 locus of Zea mays, identified as one of the genes affecting anthocyanin biosynthesis, was cloned using the transposable elements rcy and dSpm as gene tags...
- The sequence of the zein regulatory gene opaque-2 (O2) of Zea MaysM Maddaloni
Istituto Sperimentale per la Cerealieoltura, Bergamo, Italy
Nucleic Acids Res 17:7532. 1989
- Sequencing, expression pattern and RFLP mapping of a senescence-enhanced cDNA from Zea mays with high homology to oryzain gamma and aleurainC M Griffiths
Cell Biology Department, Institute for Grassland and Environmental Research, Aberystwyth, Wales, UK
Plant Mol Biol 34:815-21. 1997Sequence analysis of a 1.4 kb clone from a cDNA library of senescing Zea mays leaves reveals an open reading frame for a 360 amino acid protein...
- Isolation and characterization of the zSSIIa and zSSIIb starch synthase cDNA clones from maize endospermC Harn
Department of Food Science, New Jersey Agricultural Experiment Station, Cook College, Rutgers University, New Brunswick 08901 8520, USA
Plant Mol Biol 37:639-49. 1998Two starch synthase clones, zSSIIa and zSSIIb, were isolated from a cDNA library constructed from W64A maize endosperm...
- The fasciated ear2 gene encodes a leucine-rich repeat receptor-like protein that regulates shoot meristem proliferation in maizeF Taguchi-Shiobara
Cold Spring Harbor Laboratory, Cold Spring Harbor, New York 11724, USA
Genes Dev 15:2755-66. 2001..To understand how this regulation is achieved, we isolated a novel mutant of maize, fasciated ear2 (fea2), which causes a massive overproliferation of the ear inflorescence meristem and a more ..
- Maize HSP101 plays important roles in both induced and basal thermotolerance and primary root growthJorge Nieto-Sotelo
Department of Plant Molecular Biology, Institute of Biotechnology, National Autonomous University of Mexico, 62250 Cuernavaca, Morelos, Mexico
Plant Cell 14:1621-33. 2002..We found that maize HSP101 accumulated in mature kernels in the absence of heat stress...
- Group II intron splicing factors derived by diversification of an ancient RNA-binding domainGerard J Ostheimer
Institute of Molecular Biology, Department of Chemistry, University of Oregon, Eugene, OR 97403, USA
EMBO J 22:3919-29. 2003..previously identified CRS1 and CRS2 as host-encoded proteins required for the splicing of group II introns in maize chloroplasts...
- The maize (Zea mays L.) RTCS gene encodes a LOB domain protein that is a key regulator of embryonic seminal and post-embryonic shoot-borne root initiationGraziana Taramino
DuPont Crop Genetics Research, Experimental Station, PO Box 80353, Wilmington, DE 19880 0353, USA
Plant J 50:649-59. 2007b>Maize has a complex root system composed of different root types formed during different stages of development...
- Molecular and biochemical analysis of the plastidic ADP-glucose transporter (ZmBT1) from Zea maysSimon Kirchberger
Abteilung Pflanzenphysiologie, Fachbereich Biologie, Technische Universitat Kaiserslautern, P O Box 3049, D 67653 Kaiserslautern, Germany
J Biol Chem 282:22481-91. 2007Physiological studies on the Brittle1 maize mutant have provided circumstantial evidence that ZmBT1 (Zea mays Brittle1 protein) is involved in the ADP-Glc transport into maize endosperm plastids, but up to now, no direct ADP-Glc transport ..
- Cloning, characterization, and transformation of the phosphoethanolamine N-methyltransferase gene (ZmPEAMT1) in maize (Zea mays L.)Suowei Wu
The State Key Laboratory of Plant Genomics, Institute of Genetics and Developmental Biology, Chinese Academy of Sciences, Beijing, 100101, China
Mol Biotechnol 36:102-12. 2007..1.1.103). Herein we report the cloning and characterization of the novel maize phosphoethanolamine N-methyltransferase gene (ZmPEAMT1) using a combination of bioinformatics and a PCR-based ..
- The involvement of phospholipases C and D in the asymmetric division of subsidiary cell mother cells of Zea maysPanagiotis Apostolakos
Department of Botany, Faculty of Biology, University of Athens, Athens, Greece
Cell Motil Cytoskeleton 65:863-75. 2008..phospholipase C and D (PLC and PLD) pathways in the asymmetric divisions that produce the stomatal complexes of Zea mays was investigated...
- ZmHO-1, a maize haem oxygenase-1 gene, plays a role in determining lateral root developmentBin Han
Rubber Research Institute, Chinese Academy of Tropical Agricultural Sciences, Hainan 571737, China
Plant Sci 184:63-74. 2012..In this report, a cDNA for the gene ZmHO-1, encoding an HO-1 protein, was cloned from Zea mays seedlings...
- Characterization of profilin polymorphism in pollen with a focus on multifunctionalityJose C Jimenez-Lopez
Department of Biochemistry, Cell and Molecular Biology of Plants, Estacion Experimental del Zaidin, High Council for Scientific Research, Granada, Spain
PLoS ONE 7:e30878. 2012..Ole e 2), Betula pendula (Bet v 2), Phleum pratense (Phl p 12), Zea mays (Zea m 12) and Corylus avellana (Cor a 2)...
- Ribulose-1,5-bis-phosphate carboxylase/oxygenase accumulation factor1 is required for holoenzyme assembly in maizeLeila Feiz
Boyce Thompson Institute for Plant Research, Cornell University, Ithaca, New York 14853, USA
Plant Cell 24:3435-46. 2012..Here, we report the identification of a chloroplast protein required for Rubisco accumulation in maize (Zea mays), RUBISCO ACCUMULATION FACTOR1 (RAF1), which lacks any characterized functional domains...
- Overexpression of Arabidopsis molybdenum cofactor sulfurase gene confers drought tolerance in maize (Zea mays L.)Yao Lu
State Key Laboratory of Plant Physiology and Biochemistry, College of Agronomy and Biotechnology, China Agricultural University, Beijing, People s Republic of China
PLoS ONE 8:e52126. 2013..Transgenic maize (Zea mays L...
- cDNA clones encoding Arabidopsis thaliana and Zea mays mitochondrial chaperonin HSP60 and gene expression during seed germination and heat shockT K Prasad
Department of Botany, Iowa State University, Ames 50011
Plant Mol Biol 18:873-85. 1992..and sequenced full-length complementary DNAs coding for this mitochondrial chaperonin in Arabidopsis thaliana and Zea mays. Southern-blot analysis indicates the presence of a single hsp60 gene in the genome of A. thaliana...
- Molecular cloning and structural analysis of a gene from Zea mays (L.) coding for a putative receptor for the plant hormone auxinT Hesse
Max Planck Institut fur Zuchtungsforschung, Koln, FRG
EMBO J 8:2453-61. 1989The major auxin-binding protein from maize coleoptiles was purified to homogeneity. The protein has an apparent mol. wt of 22 kd and binds 1-naphthylacetic acid with a KD of 2.40 x 10(-7) M...
- The Etched1 gene of Zea mays (L.) encodes a zinc ribbon protein that belongs to the transcriptionally active chromosome (TAC) of plastids and is similar to the transcription factor TFIISOswaldo da Costa e Silva
Institut für Allgemeine Botanik und Botanischer Garten, Universitat Hamburg, Ohnhorststr 18, D 22 609 Hamburg, Germany
Plant J 38:923-39. 2004Etched1 (et1) is a pleiotropic, recessive mutation of maize that causes fissured and cracked mature kernels and virescent seedlings...
- Influence of transposable elements on the structure and function of the A1 gene of Zea maysZ Schwarz-Sommer
Max Planck Institut fur Zuchtungsforschung, 5000 Köln 30, FRG
EMBO J 6:287-94. 1987The structure of the A1 gene of Zea mays was determined by sequencing cDNA and genomic clones. The gene is composed of four exons and three short introns. The 40.1-kd A1 protein is an NADPH-dependent reductase...
- A member of the maize isopentenyl transferase gene family, Zea mays isopentenyl transferase 2 (ZmIPT2), encodes a cytokinin biosynthetic enzyme expressed during kernel development. Cytokinin biosynthesis in maizeNorbert Brugière
Discovery Group Agronomic Traits, Pioneer Hi Bred International, Inc, A DuPont Business, Johnston, IA 50131 0522, USA
Plant Mol Biol 67:215-29. 2008..In maize, CKs are thought to play an important role in establishing seed size and increasing seed set under normal and ..
- Cloning and expression analysis of some genes involved in the phosphoinositide and phospholipid signaling pathways from maize (Zea mays L.)Zhenhua Sui
School of Life Science, Shandong University, Jinan 250100, People s Republic of China
Gene 426:47-56. 2008..However, little is known about the phosphoinositide and phospholipid signaling pathways in maize (Zea mays L.)...
- Molecular interactions of ROOTLESS CONCERNING CROWN AND SEMINAL ROOTS, a LOB domain protein regulating shoot-borne root initiation in maize (Zea mays L.)Christine Majer
ZMBP, Center for Plant Molecular Biology, Department of General Genetics, University of Tuebingen, Auf der Morgenstelle 28, 72076 Tuebingen, Germany
Philos Trans R Soc Lond B Biol Sci 367:1542-51. 2012..encodes a LATERAL ORGAN BOUNDARIES domain (LBD) protein that regulates shoot-borne root initiation in maize (Zea mays L.)...
- The profilin multigene family of maize: differential expression of three isoformsC J Staiger
Department of Cell Biology, John Innes Centre for Plant Science Research, Norwich, UK
Plant J 4:631-41. 1993..Here we have identified and characterized three members of the profilin multigene family from the plant Zea mays. Two cDNAs isolated from a maize pollen library (ZmPRO 1 and ZmPRO 3) each have a single, large open reading ..
- Metabolic regulation of asparagine synthetase gene expression in maize (Zea mays L.) root tipsC Chevalier
Station de Physiologie Végétale, Institut National de la Recherche Agronomique, Villenave D Ornon, France
Plant J 9:1-11. 1996Differential hybridization of a cDNA library constructed with poly(A)+ mRNA from 24 h starved maize (Zea mays L.) root tips, resulted in the isolation of a cDNA (called pZSS1) that was highly induced during glucose deprivation...
- Root-specific expression of a Zea mays gene encoding a novel glycine-rich protein, zmGRP3M L Goddemeier
University of Freiburg, Institute of Biology III, Germany
Plant Mol Biol 36:799-802. 1998The isolation and characterization of a cDNA clone from Zea mays coding for a novel glycine-rich protein (GRP) is described. The corresponding 1...
- Characterization of a maize heat-shock protein 101 gene, HSP101, encoding a ClpB/Hsp100 protein homologueJ Nieto-Sotelo
Instituto de Biotecnologia, Universidad Nacional Autonoma de Mexico, Department of Plant Molecular Biology, Apdo Postal 510 3, Cuernavaca, Mor, 62250, Mexico
Gene 230:187-95. 1999Heat shock protein 101 (HSP101) cDNA and genomic clones from maize have been isolated. The structure of maize HSP101 reveals the presence of six exons interrupted by five introns...
- Maize profilin isoforms are functionally distinctD R Kovar
Department of Biological Sciences, Purdue University, West Lafayette, Indiana 47907, USA
Plant Cell 12:583-98. 2000..In this study, an analysis of native and recombinant proteins from maize demonstrates the existence of two classes of functionally distinct profilin isoforms...
- Diversification in substrate usage by glutathione synthetases from soya bean (Glycine max), wheat (Triticum aestivum) and maize (Zea mays)Mark Skipsey
Crop Protection Group, School of Biological and Biomedical Sciences, University of Durham, South Road, Durham DH1 3LE, UK
Biochem J 391:567-74. 2005..wheat (hydroxymethylglutathione or gamma-glutamyl-L-cysteinyl-serine) and maize (gamma-Glu-Cys-Glu)...
- Nitrogen metabolism in the developing ear of maize (Zea mays): analysis of two lines contrasting in their mode of nitrogen managementRafael A Cañas
Unité de Nutrition Azotée des Plantes, Institut Jean Pierre Bourgin, Institut National de la Recherche Agronomique, F 78026 Versailles Cedex, France
New Phytol 184:340-52. 2009The main steps of nitrogen (N) metabolism were characterized in the developing ear of the two maize (Zea mays) lines F2 and Io, which were previously used to investigate the genetic basis of nitrogen use efficiency (NUE) in relation to ..
- Cloning and characterization of a cDNA encoding a maize seedling phytaseS Maugenest
Laboratoire de Biologie des Semences, INRA INA PG, Versailles, France
Biochem J 322:511-7. 1997During germination, maize seedlings express a phytase able to hydrolyse the large amount of phytin stored in the dry seed...
- Genomic organization and promoter activity of the maize starch branching enzyme I geneK N Kim
Intercollege Graduate Programs in Plant Physiology, Genetics, The Biotechnology Institute, Department of Horticulture, The Pennsylvania State University, University Park, Pennsylvania, PA 16802, USA
Gene 216:233-43. 1998..In maize (Zea mays L...
- Purification and molecular genetic characterization of ZPU1, a pullulanase-type starch-debranching enzyme from maizeM K Beatty
Department of Biochemistry, Biophysics, and Molecular Biology, Iowa State University, Ames 50011, USA
Plant Physiol 119:255-66. 1999..purified specific isoamylase- and pullulanase-type starch-debranching enzymes (DBEs) present in developing maize (Zea mays L.) endosperm. The cDNA clone Zpu1 was isolated based on its homology with a rice (Oryza sativa L...
- Cloning and sequencing of the casein kinase 2 alpha subunit from Zea maysG Dobrowolska
Institute of Biochemistry and Biophysics, Polish Academy of Sciences, Warsaw
Biochim Biophys Acta 1129:139-40. 1991The nucleotide sequence of the cDNA coding for the alpha subunit of casein kinase 2 of Zea mays has been determined. The cDNA clone contains an open reading frame of 996 nucleotides encoding a polypeptide comprising 332 amino acids...
- A SecY homologue is required for the elaboration of the chloroplast thylakoid membrane and for normal chloroplast gene expressionL M Roy
Institute of Molecular Biology, University of Oregon, Eugene, Oregon 97403, USA
J Cell Biol 141:385-95. 1998..To explore the role of cpSecY, we obtained maize mutants with transposon insertions in the corresponding gene...
- Mechanisms by which a fungal HDAC inhibitor suppresses innate immunity in maizeJUSTIN WILLIAM WALLEY; Fiscal Year: 2012..One devastating disease of Zea mays (corn) is caused by the fungal pathogen Cochliobolus carbonum. Intriguingly, the main determinant of C...
- GENETICS OF SEX DETERMINATION AND CELL DEATH IN PLANTSStephen Dellaporta; Fiscal Year: 2004..of this program is to understand the fundamental mechanisms or sex determination in the model genetic organism Zea mays (maize), a species that produces unisexual flowers (called "florets") through the action of sex determination (SD)..
- Environmental Stresses on Protein Structure of the Repair Response in Higher PlanSARAH VILLA; Fiscal Year: 2007..Since light induced oxidation reactions may regulate the expression of PIMT in Zea mays (corn), the endogenous PIMT activity will be measured in homogenates from corn plants grown under high light ..
- ANALYSIS OF THE ANAEROBIC-STRESS RESPONSE IN MAIZEMartin Sachs; Fiscal Year: 1992I propose to study the anaerobic-stress response in Zea mays. Anaerobic treatment dramatically alters the pattern of gene expression in maize seedlings...
- Gene expression effects of heterosis and ploidy levelNICOLE RIDDLE; Fiscal Year: 2005..Focusing mainly on the use of microarrays and gene expression analysis in Zea mays, the proposed experiments will allow us collect the necessary data to develop a molecular model for heterosis...
- REGULATORY MECHANISMS OF AN INDUCIBLE GENEJohn Walker; Fiscal Year: 1992..required for the transcription expression of a specific set of genes during conditions of low oxygen-stress in Zea mays. Low-oxygen stress overrides the normal developmental program of gene expression and induces the synthesis of a ..
- VARIATION IN MITOCHONDRIAL GENOTYPE AND PHENOTYPEVirginia Walbot; Fiscal Year: 1980We propose a model of mitochondrial DNA organization in Zea mays of multiple, circular chromosomes of variable ploidy. Variant mitochondrial DNA organization correlates with whole organism male sterility and sensitivity to fungal toxins...
- MUTATOR TRANSPORTABLE ELEMENTS OF MAIZEVirginia Walbot; Fiscal Year: 2005..The MuDR/Mu (Mutator) transposons of maize move by a "cut and paste" mechanism in somatic tissues, very late in development resulting in a wide spectrum of ..
- MEMBRANE FUNCTION IN MUTANTS OF CAENORHABDITIS ELEGANSJohn Browse; Fiscal Year: 2004..Quantitative measures of low-temperature performance and thermotolerance of the range of desaturase mutants will be correlated with fatty acid composition and measurements of membrane fluidity. ..
- ALIGNMENT BASED METHODS FOR MOLECULAR SEQUENCE ANALYSISSteven Henikoff; Fiscal Year: 2001..This effort could yield new eukaryotic family members of great importance for understanding epigenetic phenomena, some of which, such as parental imprinting, are relevant to human disease. ..
- Maintenance of blocks-based tools for functional genomicSteven Henikoff; Fiscal Year: 2006..These various components will be packaged to facilitate updates and local implementations. [unreadable] [unreadable]..
- Genetics of Variation for Complex TraitsJohn Doebley; Fiscal Year: 2007..genetic, developmental and molecular basis of naturally occurring variation for complex morphological traits using maize as the model system...
- Comparative Genomics in the EnterobateriaceaeSandra Clifton; Fiscal Year: 2009....
- Molecular Mechanisms of Genome DuplicationZENGJIAN CHEN; Fiscal Year: 2009..abstract_text> ..
- FUNCTIONAL ANALYSIS OF MAIZE GROUP-1 POLLEN ALLERGENSDaniel Cosgrove; Fiscal Year: 2004..25 percentof the US population. We recently discovered that the group-I allergen from maize pollen (called Zea ml) loosens the extracellular matrix (wall) of the grass stigma...
- Mammalian Lactoferrin Receptors: Structure and FunctionBo Lonnerdal; Fiscal Year: 2007..Overall, our understanding of the physiological significance of Lf and its receptor will be increased. ..
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