G RoederSummaryAffiliation: Yale University Country: USA Publications
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Publications
Organization of the yeast Zip1 protein within the central region of the synaptonemal complexH Dong
Department of Molecular, Cellular and Developmental Biology, Howard Hughes Medical Institute, Yale University, New Haven, Connecticut 06520 8103, USA
J Cell Biol 148:417-26. 2000..Together, these results suggest that two Zip1 dimers, lying head-to-head, span the width of the SC...
The pachytene checkpointG S Roeder
Howard Hughes Medical Institute, Yale University, PO Box 208103, New Haven, CT 06520 8103, USA
Trends Genet 16:395-403. 2000..Progress has been made in identifying components of the cell-cycle machinery that are impacted by the checkpoint...
Meiotic chromosomes: it takes two to tangoG S Roeder
Department of Molecular, Cellular, and Developmental Biology, Yale University, New Haven, Connecticut 06520-8103 USA
Genes Dev 11:2600-21. 1997
Bdf1, a yeast chromosomal protein required for sporulationP Chua
Department of Biology, Yale University, New Haven, Connecticut 06520 8103, USA
Mol Cell Biol 15:3685-96. 1995..We propose that the Bdf1 protein is a component of chromatin and that the mitotic and meiotic defects of the bdf1 null mutant result from alterations in chromatin structure...
Pch2 links chromatin silencing to meiotic checkpoint controlP A San-Segundo
Howard Hughes Medical Institute, and Department of Molecular, Cellular, and Developmental Biology, Yale University, New Haven, Connecticut 06520 8103, USA
Cell 97:313-24. 1999..Under certain circumstances, Sir3-dependent localization of Pch2 to telomeres also provides checkpoint function. These unexpected findings link the nucleolus, chromatin silencing, and the pachytene checkpoint...
Zip3 provides a link between recombination enzymes and synaptonemal complex proteinsS Agarwal
Howard Hughes Medical Institute, Department of Molecular, Cellular and Developmental Biology, Yale University, New Haven, Connecticut 06520, USA
Cell 102:245-55. 2000..We speculate that Zip3 is a component of recombination nodules and serves to link the initiation of synapsis to meiotic recombination...
Bypass of a meiotic checkpoint by overproduction of meiotic chromosomal proteinsJ M Bailis
Department of Molecular, Cellular, and Developmental Biology, Yale University, New Haven, CT 06520 8103, USA
Mol Cell Biol 20:4838-48. 2000....
Pachytene exit controlled by reversal of Mek1-dependent phosphorylationJ M Bailis
Department of Molecular, Cellular, and Developmental Biology, Yale University, New Haven, Connecticut 06520, USA
Cell 101:211-21. 2000..We speculate that phosphorylated Red1 prevents exit from pachytene and that completion of meiotic recombination triggers Glc7-dependent dephosphorylation of Red1...
Zip2, a meiosis-specific protein required for the initiation of chromosome synapsisP R Chua
Department of Molecular, Cellular, and Developmental Biology, Yale University, New Haven, Connecticut 06520 8103, USA
Cell 93:349-59. 1998..We propose that Zip2p promotes the initiation of chromosome synapsis and that localization of Zip2p to sites of interhomolog recombination ensures synapsis between homologous chromosomes...
The meiosis-specific Hop2 protein of S. cerevisiae ensures synapsis between homologous chromosomesJ Y Leu
Department of Molecular, Cellular, and Developmental Biology, Yale University, New Haven, Connecticut 06520 8103, USA
Cell 94:375-86. 1998..We propose that the Hop2 protein functions to prevent synapsis between nonhomologous chromosomes...
The rec102 mutant of yeast is defective in meiotic recombination and chromosome synapsisJ Bhargava
Department of Biology, Yale University, New Haven, Connecticut 06511 8112
Genetics 130:59-69. 1992..The REC102 gene was cloned based on complementation of the mutant defect and the gene was mapped to chromosome XII between CDC25 and STE11...
Roles for two RecA homologs in promoting meiotic chromosome synapsisB Rockmill
Department of Biology, Yale University, New Haven, Connecticut 06520 8103, USA
Genes Dev 9:2684-95. 1995..In a zip1 haploid, axial associations are not apparent, suggesting that these associations depend on interactions between homologous sequences...
Synaptonemal complex morphogenesis and sister-chromatid cohesion require Mek1-dependent phosphorylation of a meiotic chromosomal proteinJ M Bailis
Department of Molecular, Cellular and Developmental Biology, Yale University, New Haven, Connecticut 06520 8103 USA
Genes Dev 12:3551-63. 1998..Fluorescent in situ hybridization analysis indicates that Mek1-mediated phosphorylation of Red1 is required for meiotic sister-chromatid cohesion, raising the possibility that cohesion is regulated by protein phosphorylation...
A meiosis-specific protein kinase homolog required for chromosome synapsis and recombinationB Rockmill
Department of Biology, Yale University, New Haven, Connecticut 06511 8112
Genes Dev 5:2392-404. 1991..The sequence of the MEK1 gene predicts a 56.8-kD protein with homology to serine-threonine protein kinases. The MEK1 gene maps to chromosome XV, 13 cM proximal to CDC64. Models for the function of the MEK1 gene product are proposed...
Tam1, a telomere-associated meiotic protein, functions in chromosome synapsis and crossover interferenceP R Chua
Department of Molecular, Cellular and Developmental Biology, Yale University, New Haven, Connecticut 06520 8103, USA
Genes Dev 11:1786-800. 1997..We discuss here possibilities for how a telomere-associated protein might function in chromosome synapsis and crossover interference...
The pachytene checkpoint prevents accumulation and phosphorylation of the meiosis-specific transcription factor Ndt80K S Tung
Howard Hughes Medical Institute, Yale University, New Haven, CT 06520 8103, USA
Proc Natl Acad Sci U S A 97:12187-92. 2000..Our results indicate that inhibition of Ndt80 activity is one mechanism used to achieve pachytene arrest...
The pachytene checkpoint in S. cerevisiae depends on Swe1-mediated phosphorylation of the cyclin-dependent kinase Cdc28J Y Leu
Department of Molecular, Cellular, and Developmental Biology, Yale University, New Haven, Connecticut 06520 8103, USA
Mol Cell 4:805-14. 1999..The requirement for Swe1 distinguishes the pachytene checkpoint from the DNA damage checkpoints operating in vegetative cells...
The yeast MER2 gene is required for chromosome synapsis and the initiation of meiotic recombinationB Rockmill
Department of Biology, Yale University, New Haven, Connecticut 06520 8103, USA
Genetics 141:49-59. 1995..We suggest that the primary defect in the mer2 mutant is in the initiation of meiotic genetic exchange...
Meiotic gene conversion and crossing over: their relationship to each other and to chromosome synapsis and segregationJ Engebrecht
Department of Biology, Yale University, New Haven, Connecticut 06511 8112
Cell 62:927-37. 1990..One interpretation of this result is that only those crossovers that occur in the context of the synaptonemal complex lead to the establishment of functional chiasmata. The MER2 gene product is essential for meiosis...
Expression and DNA sequence of RED1, a gene required for meiosis I chromosome segregation in yeastE A Thompson
Department of Biology, Yale University, New Haven, CT 06511 8112
Mol Gen Genet 218:293-301. 1989..5 kilodaltons. There is no significant homology between the RED1 amino acid sequence and other known protein sequences, including those encoded by genes essential for meiosis...
Yeast mer1 mutants display reduced levels of meiotic recombinationJ Engebrecht
Department of Biology, Yale University, New Haven, Connecticut 06511
Genetics 121:237-47. 1989..Strains carrying disruptions of the MER1 gene are mitotically viable. The epistatic relationships between MER1 and previously characterized meiotic genes are described...
MEI4, a yeast gene required for meiotic recombinationT M Menees
Department of Biology, Yale University, New Haven, Connecticut 06511 8112
Genetics 123:675-82. 1989..The mei4 mutation is able to rescue the spore-inviability phenotype of spo13 and 52 strains (i.e., mei4 spo13 rad52 mutants produce viable spores), indicating that MEI4 acts before RAD52 in the meiotic recombination pathway...
Role for the silencing protein Dot1 in meiotic checkpoint controlP A San-Segundo
Howard Hughes Medical Institute, Department of Molecular, Cellular and Developmental Biology, Yale University, New Haven, Connecticut 06520 8103, USA
Mol Biol Cell 11:3601-15. 2000..In vegetative cells, mutation of DOT1 results in delocalization of Sir3 from telomeres, accounting for the impaired telomeric silencing in dot1...
MEI4, a meiosis-specific yeast gene required for chromosome synapsisT M Menees
Department of Biology, Yale University, New Haven, Connecticut 06511 8112
Mol Cell Biol 12:1340-51. 1992..Cytological analysis of mei4 mutant strains during meiotic prophase demonstrates that the chromosomes form long axial elements that fail to undergo synapsis. The meiosis II division is delayed in mei4 strains...
Meiotic chromosome morphology and behavior in zip1 mutants of Saccharomyces cerevisiaeK S Tung
Howard Hughes Medical Institute, Yale University, New Haven, Connecticut 06520 8103, USA
Genetics 149:817-32. 1998..In contrast, the role of Zip1p in synapsis is separable from its role in meiotic cell cycle progression. zip1 mutants display interval-specific effects on crossing over...
Meiosis-specific RNA splicing in yeastJ A Engebrecht
Department of Biology, Yale University, New Haven, Connecticut 06511 8112
Cell 66:1257-68. 1991..Therefore, at least one of the functions of the MER1 protein is to mediate splicing of the MER2 transcript. Genetic data suggest that the MER1 gene may also be responsible for splicing the transcript of at least one other gene...
The budding yeast Msh4 protein functions in chromosome synapsis and the regulation of crossover distributionJ E Novak
Department of Molecular, Cellular and Developmental Biology, Yale University, New Haven, Connecticut 06520 8103, USA
Genetics 158:1013-25. 2001..Both Zip2 and Zip1 are required for the normal localization of Msh4 to chromosomes, raising the possibility that the zip1 and zip2 defects in crossing over are indirect, resulting from the failure to localize Msh4 properly...
Binding of a cell-type-specific RNA splicing factor to its target regulatory sequenceK Nandabalan
Department of Biology, Yale University, New Haven, Connecticut 06520 8103
Mol Cell Biol 15:1953-60. 1995..RNase T1 footprinting indicates that the Mer1 protein contacts MER2 RNA at several points in the 5' exon and in the intron. Thus, Mer1 interacts directly with a regulatory element in MER2 RNA and promotes splicing...
Large-scale analysis of gene expression, protein localization, and gene disruption in Saccharomyces cerevisiaeN Burns
Department of Biology, Yale University, New Haven, Connecticut 06520 8103
Genes Dev 8:1087-105. 1994..Our results will allow researchers who identify a yeast gene to determine immediately whether that gene is expressed at a specific time during the life cycle and whether its gene product localizes to a specific subcellular location...
Mutations in U1 snRNA bypass the requirement for a cell type-specific RNA splicing factorK Nandabalan
Department of Biology, Yale University, New Haven, Connecticut 06511 8112
Cell 73:407-15. 1993..When this nucleotide is mutated to restore the consensus, base pairing with U1 snRNA is increased and the requirement for MER1 is alleviated...
A multipurpose transposon system for analyzing protein production, localization, and function in Saccharomyces cerevisiaeP Ross-MacDonald
Department of Biology, Yale University, New Haven, CT 06520 8103, USA
Proc Natl Acad Sci U S A 94:190-5. 1997..We demonstrate these features of the transposons by mutagenesis of the SPA2, ARP100, SER1, and BDF1 genes...
The yeast Red1 protein localizes to the cores of meiotic chromosomesA V Smith
Department of Biology, Yale University, New Haven, Connecticut 06520 8103, USA
J Cell Biol 136:957-67. 1997..These observations are consistent with previous genetic studies suggesting that Red1 and Hop1 directly interact. There is little or no Hop1 protein on pachytene chromosomes or in synapsed chromosomal regions...
Zip1-induced changes in synaptonemal complex structure and polycomplex assemblyM Sym
Department of Biology, Yale University, New Haven, Connecticut 06520 8103
J Cell Biol 128:455-66. 1995..Our results demonstrate that Zip1 is a structural component of the central region of the SC. More specifically, we speculate that Zip1 is a component of the transverse filaments that lie perpendicular to the long axis of the complex...
RED1: a yeast gene required for the segregation of chromosomes during the reductional division of meiosisB Rockmill
Department of Biology, Yale University, New Haven, CT 06511
Proc Natl Acad Sci U S A 85:6057-61. 1988..We propose that the RED1 gene product is involved in meiosis I chromosome disjunction, perhaps by maintaining the connections between homologous chromosomes through metaphase I...
Cloning and characterization of the Kluyveromyces lactis homologs of the Saccharomyces cerevisiae RED1 and HOP1 genesA V Smith
Howard Hughes Medical Institute, Department of Molecular, Cellular and Developmental Biology, Yale University, New Haven, CT 06520 8103, USA
Chromosoma 109:50-61. 2000..Unlike the S. cerevisiae RED1 gene, the K. lactis RED1 contains an intron; the transcript of the K. lactis gene is efficiently spliced during meiosis in S. cerevisiae...
The sep1 mutant of Saccharomyces cerevisiae arrests in pachytene and is deficient in meiotic recombinationD X Tishkoff
Dana Farber Cancer Institute, Department of Biological Chemistry and Molecular Pharmacology, Harvard Medical School, Boston, Massachusetts 02115, USA
Genetics 139:495-509. 1995..We hypothesize that the Sep1 protein participates directly in meiotic recombination and that other strand exchange enzymes, acting in parallel recombination pathways, are able to substitute partially for the absence of the Sep1 protein...
Research Grants
- MOLECULAR MECHANISMS OF GENETIC RECOMBINATION IN YEASTG Roeder; Fiscal Year: 1993..Some of the meiotic recombination genes will be cloned and sequenced; expression of the cloned genes will be examined through the construction and analysis of lacZ fusion genes...
- Chromosome Synapsis and Meiotic Cell Cycle RegulationG Roeder; Fiscal Year: 2005..Activity of the Cdcl4 phosphatase is regulated by sequestration in the nucleolus. The possibility that Pch2 regulates Cdcl4 activity will be tested by examining the effects of Cdcl4 inactivation and overproduction. ..
