Research Topics
Genomes and Genes | X LinSummaryAffiliation: Baylor College of Medicine Country: USA Publications
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Publications
Smad6 recruits transcription corepressor CtBP to repress bone morphogenetic protein-induced transcriptionXia Lin
Michael E DeBakey Department of Surgery, Baylor College of Medicine, One Baylor Plaza, Room 131D, Houston, TX 77030, USA
Mol Cell Biol 23:9081-93. 2003..We conclude that the nuclear functions and physical interaction of Smad6 and CtBP provide a novel mechanism for the transcriptional regulation by inhibitory Smads...
Abrogation of transforming growth factor-beta signaling in pancreatic cancerXia Lin
Michael E DeBakey Department of Surgery, Baylor College of Medicine, Room 131D, Houston, Texas 77030, USA
World J Surg 29:312-6. 2005..In this review, we summarize recent research progress on TGFbeta signaling and pancreatic cancer...
Smurf2 is a ubiquitin E3 ligase mediating proteasome-dependent degradation of Smad2 in transforming growth factor-beta signalingX Lin
Departments of Surgery and Molecular and Cellular Biology, Baylor College of Medicine, Houston, Texas 77030, USA
J Biol Chem 275:36818-22. 2000..Consistent with these results, Smurf2 potently reduced the transcriptional activity of Smad2. These data suggest that a ubiquitin/proteasome-dependent mechanism is important for proper regulation of TGF-beta signaling...
Direct interaction of c-Myc with Smad2 and Smad3 to inhibit TGF-beta-mediated induction of the CDK inhibitor p15(Ink4B)Xin Hua Feng
Michael E DeBakey Department of Surgery, Baylor College of Medicine, Houston, TX 77030, USA
Mol Cell 9:133-43. 2002..These results suggest that oncogenic c-Myc promotes cell growth and cancer development partly by inhibiting the growth inhibitory functions of Smads...
Fluorescent probes attached to Cys 35 or Cys 84 in cardiac troponin C are differentially sensitive to Ca(2+)-dependent events in vitro and in situJ A Putkey
Department of Biochemistry and Molecular Biology, University of Texas Medical School, Houston 77225, USA
Biochemistry 36:970-8. 1997....
Smad2, Smad3 and Smad4 cooperate with Sp1 to induce p15(Ink4B) transcription in response to TGF-betaX H Feng
Departments of Growth and Development and Anatomy, and Programs in Cell Biology and Developmental Biology, University of California, San Francisco, CA 94143 0640, USA
EMBO J 19:5178-93. 2000..These findings explain the tumor suppressor roles of Smad2 and Smad4 in growth arrest signaling by TGF-beta...
SUMO-1/Ubc9 promotes nuclear accumulation and metabolic stability of tumor suppressor Smad4Xia Lin
Michael E DeBakey Department of Surgery, Baylor College of Medicine, Houston, Texas 77030, USA
J Biol Chem 278:31043-8. 2003....
Critical regulation of TGFbeta signaling by Hsp90Katharine H Wrighton
Michael E DeBakey Department of Surgery, Baylor College of Medicine, Houston, TX 77030, USA
Proc Natl Acad Sci U S A 105:9244-9. 2008..Our data reveal an essential level of TGFbeta signaling regulation mediated by Hsp90 by its ability to chaperone TbetaRs and also implicate the use of Hsp90 inhibitors in blocking undesired activation of TGFbeta signaling in diseases...
Opposed regulation of corepressor CtBP by SUMOylation and PDZ bindingXia Lin
Michael E DeBakey Department of Surgery, Baylor College of Medicine, Houston, TX 77030, USA
Mol Cell 11:1389-96. 2003..This study identifies SUMOylation as a regulatory mechanism underlying CtBP1-dependent transcriptional repression...
Small C-terminal domain phosphatases dephosphorylate the regulatory linker regions of Smad2 and Smad3 to enhance transforming growth factor-beta signalingKatharine H Wrighton
Michael E DeBakey Department of Surgery, Baylor College of Medicine, One Baylor Plaza, Houston, TX 77030, USA
J Biol Chem 281:38365-75. 2006..Taken together, this work identifies the first example of a Smad2/3 linker phosphatase(s) and reveals an important new substrate for SCPs...
Activation of transforming growth factor-beta signaling by SUMO-1 modification of tumor suppressor Smad4/DPC4Xia Lin
Michael E DeBakey Department of Surgery, Baylor College of Medicine, Houston, Texas 77030, USA
J Biol Chem 278:18714-9. 2003..2 promoter. Importantly, SUMO-1 overexpression enhanced TGF-beta-induced transcriptional responses. These findings identify sumoylation as a unique mechanism to modulate Smad4-dependent cellular responses...
Nuclear export of Smad2 and Smad3 by RanBP3 facilitates termination of TGF-beta signalingFangyan Dai
Department of Molecular and Cellular Biology, Baylor College of Medicine, Houston, TX 77030, USA
Dev Cell 16:345-57. 2009..In conclusion, our study supports a definitive role for RanBP3 in mediating Smad2/3 nuclear export and terminating TGF-beta signaling...
PPM1A functions as a Smad phosphatase to terminate TGFbeta signalingXia Lin
Michael E DeBakey Department of Surgery, Baylor College of Medicine, Houston, TX 77030, USA
Cell 125:915-28. 2006..This work demonstrates that PPM1A/PP2Calpha, through dephosphorylation of Smad2/3, plays a critical role in terminating TGFbeta signaling...
Ubiquitination and proteolysis of cancer-derived Smad4 mutants by SCFSkp2Min Liang
Department of Molecular and Cellular Biology, Baylor College of Medicine, One Baylor Plaza, Room 137D, Houston, TX 77030, USA
Mol Cell Biol 24:7524-37. 2004..These results suggest an important role for the SCFSkp2 complex in switching cancer mutants of Smad4 to undergo polyubiquitination-dependent degradation...
Regulation of Smad4 sumoylation and transforming growth factor-beta signaling by protein inhibitor of activated STAT1Min Liang
Michael E DeBakey Department of Surgery, Baylor College of Medicine, Houston, Texas 77030, USA
J Biol Chem 279:22857-65. 2004..These data demonstrate that PIAS1 protein positively modulates TGF-beta responses as a SUMO E3 ligase for Smad4...
Resistance to transforming growth factor-beta occurs in the presence of normal Smad activationDavid H Berger
Department of Surgery, The Baylor College of Medicine, Houston, Tex, USA
Surgery 132:310-6. 2002..In this study we hypothesized that decreased TGF-beta receptor expression leads to reduced Smad signaling and overexpression of c-Myc in intestinal epithelial (RIE) and transformed intestinal epithelial cells (RIE-Tr) cells...
Transforming Growth Factor {beta} Can Stimulate Smad1 Phosphorylation Independently of Bone Morphogenic Protein ReceptorsKatharine H Wrighton
Michael E DeBakey Department of Surgery and Department of Molecular and Cellular Biology, Baylor College of Medicine, Houston, Texas 77030, USA
J Biol Chem 284:9755-63. 2009..Thus, TGFbeta-mediated Smad1 phosphorylation appears to occur via different receptor complexes in a cell type-specific manner...
BCL6 represses Smad signaling in transforming growth factor-beta resistanceDegang Wang
Michael E DeBakey Department of Surgery, Baylor College of Medicine, Houston, Texas 77030, USA
Cancer Res 68:783-9. 2008..This study provides strong evidence that overexpression of BCL6 contributes to TGF-beta resistance in B-cell lymphoma...
Erbin inhibits transforming growth factor beta signaling through a novel Smad-interacting domainFangyan Dai
Department of Molecular and Cellular Biology, Baylor College of Medicine, One Baylor Plaza, Room 137D, Houston, TX 77030, USA
Mol Cell Biol 27:6183-94. 2007..Therefore, these results define Erbin as a novel negative modulator of Smad2/Smad3 functions and expand the physiological role of Erbin to the regulation of TGFbeta signaling...
Phospho-control of TGF-beta superfamily signalingKatharine H Wrighton
Michael E DeBakey Department of Surgery, Department of Molecular and Cellular Biology and Dan L Duncan Cancer Center, Baylor College of Medicine, Houston, TX 77030, USA
Cell Res 19:8-20. 2009..This article illustrates the essential roles of reversible phosphorylation in controlling the strength and duration of TGF-beta signaling and the ensuing physiological responses...
Protein serine/threonine phosphatase PPM1A dephosphorylates Smad1 in the bone morphogenetic protein signaling pathwayXueyan Duan
Department of Molecular and Cellular Biology, Michael E DeBakey Department of Surgery, Baylor College of Medicine, Houston, Texas 77030, USA
J Biol Chem 281:36526-32. 2006..Collectively, our study suggests that PPM1A plays an important role in controlling BMP signaling through catalyzing Smad dephosphorylation...
Identification of a human brain-specific gene, calneuron 1, a new member of the calmodulin superfamilyY Q Wu
Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas 77030, USA
Mol Genet Metab 72:343-50. 2001....
Smad2 positively regulates the generation of Th17 cellsGustavo J Martinez
Department of Immunology and Center for Inflammation and Cancer, MD Anderson Cancer Center, Houston, Texas 77030, USA
J Biol Chem 285:29039-43. 2010..These results demonstrate that Smad2 positively regulates the generation of inflammatory Th17 cells...
Smad3 differentially regulates the induction of regulatory and inflammatory T cell differentiationGustavo J Martinez
Department of Immunology, M D Anderson Cancer Center, Houston, Texas 77054, USA
J Biol Chem 284:35283-6. 2009..These results demonstrate that Smad3 is differentially involved in the reciprocal regulatory and inflammatory T cell generation...
Termination of TGF-beta superfamily signaling through SMAD dephosphorylation--a functional genomic viewXia Lin
Michael E DeBakey Department of Surgery, Baylor College of Medicine, Houston TX 77030, USA
J Genet Genomics 34:1-9. 2007..This article briefly reviews how dynamic phosphorylation and dephosphorylation of SMADs control or fine-tune the signaling strength and duration and ultimately the physiological consequences in TGF-beta signaling...
dSmurf selectively degrades decapentaplegic-activated MAD, and its overexpression disrupts imaginal disc developmentYao Yun Liang
Michael E DeBakey Department of Surgery, Department of Molecular and Cellular Biology, Ophthalmology, Program of Developmental Biology, Baylor College of Medicine, Houston, Texas 77030, USA
J Biol Chem 278:26307-10. 2003..We conclude that dSmurf specifically targets phosphorylated MAD to proteasome-dependent degradation and regulates DPP signaling during development...
Human NDUFB9 gene: genomic organization and a possible candidate gene associated with deafness disorder mapped to chromosome 8q13X Lin
Department of Biology and Institute of Molecular Biology, University of Houston, Houston, Tex, USA
Hum Hered 49:75-80. 1999..To identify whether mutations in NDUFB9 are involved in causing the BOR syndrome, we screened 9 BOR families which did not show mutations in the EYA1 gene by heteroduplex analysis; however, no mutations were found...
Coupling of dephosphorylation and nuclear export of Smads in TGF-beta signalingFangyan Dai
Department of Molecular and Cellular Biology, Baylor College of Medicine, Houston, TX, USA
Methods Mol Biol 647:125-37. 2010..The second step involves nuclear export of dephosphorylated Smad2/3 with the aid of nuclear protein RanBP3 to terminate Smad signaling. This chapter introduces methods for examining nuclear export of Smad2/3 in TGF-beta signaling...
Smad3 mediates immediate early induction of Id1 by TGF-betaYao Yun Liang
Michael E DeBakey Department of Surgery, Baylor College of Medicine, BCM 390, Research Tower, Room R711, One Baylor Plaza, Houston, TX 77030, USA
Cell Res 19:140-8. 2009..Chromatin immunoprecipitation assay confirms that Smad3 and Smad4 bind to the upstream region of the Id1 gene. Our results demonstrate that Smad3, but not Smad2, mediates TGF-beta1-dependent early transcriptional induction of Id1...
PPM1A and PPM1B act as IKKbeta phosphatases to terminate TNFalpha-induced IKKbeta-NF-kappaB activationWenjing Sun
Texas Children s Cancer Center, Department of Pediatrics, Dan L Duncan Cancer Center, Baylor College of Medicine, Houston, TX 77030, United States
Cell Signal 21:95-102. 2009..These data suggest that PPM1A and PPM1B play an important role in the termination of TNFalpha-mediated NF-kappaB activation through dephosphorylating and inactivating IKKbeta...
Phosphatase PPM1A regulates phosphorylation of Thr-186 in the Cdk9 T-loopYan Wang
Department of Molecular Virology and Microbiology, Baylor College of Medicine, Houston, Texas 77030, USA
J Biol Chem 283:33578-84. 2008..PPM1B only efficiently dephosphorylated Cdk9 Thr-186 in vitro when 7SK RNA was depleted from P-TEFb. Taken together, our data indicate that PPM1A and to some extent PPM1B are important negative regulators of P-TEFb function...
Transforming growth factor-beta-independent regulation of myogenesis by SnoN sumoylationKatharine H Wrighton
Michael E DeBakey Department of Surgery and Department of Molecular and Cellular Biology, Baylor College of Medicine, Houston, Texas 77030, USA
J Biol Chem 282:6517-24. 2007..Our study suggests a novel role for SUMO modification in the regulation of myogenic differentiation...
Smad ubiquitination regulatory factor-2 in the fibrotic kidney: regulation, target specificity, and functional implicationRuoyun Tan
Department of Medicine, The Second Affiliated Hospital, Nanjing Medical University, Nanjing, China
Am J Physiol Renal Physiol 294:F1076-83. 2008..It appears that dysregulation of Smurf2 could contribute to an aberrant TGF-beta/Smad signaling in the pathogenesis of kidney fibrosis...
Bioconjugated nanoparticles for DNA protection from cleavageXiao-xiao He
State Key Laboratory of Chemo/Biosensing and Chemometrics, College of Chemistry and Chemical Engineering, Institute of Biological Technology, Hunan University, Changsha 410082, P. R. China
J Am Chem Soc 125:7168-9. 2003....
C. elegans serine-threonine kinase KIN-29 modulates TGFbeta signaling and regulates body size formationLisa L Maduzia
Waksman Institute, Department of Molecular Biology and Biochemistry, and Cancer Institute of New Jersey, Rutgers University, Piscataway, NJ 08854 8020, USA
BMC Dev Biol 5:8. 2005..To identify additional factors that modulate TGFbeta signaling in the Sma/Mab pathway, we have undertaken a genetic screen for small animals and have identified kin-29...
TGFbeta1 regulation of vimentin gene expression during differentiation of the C2C12 skeletal myogenic cell line requires Smads, AP-1 and Sp1 family membersYongzhong Wu
Department of Biochemistry and the Massey Cancer Center, Medical College of Virginia Campus, Virginia Commonwealth University, Richmond, VA 23298 0614, USA
Biochim Biophys Acta 1773:427-39. 2007..DNA precipitation and ChIP assays suggest that c-Jun, c-Fos, Smad3 and Sp1/Sp3 interact over this region, but this interaction changes during myogenesis with TGFbeta1 induction...
Smad7-induced beta-catenin degradation alters epidermal appendage developmentGangwen Han
Department of Otolaryngology, Oregon Health and Science University, Portland, 97239, USA
Dev Cell 11:301-12. 2006..Our data reveal a mechanism for Smad7 in antagonizing Wnt/beta-catenin signaling, thereby shifting the skin differentiation program from forming hair follicles to sebaceous glands...
Research Grants
- Regulation of SMAD2 Signaling by SMP1 PhosphataseXia Lin; Fiscal Year: 2007..The results will be pertinent towards development for a foundation for the rational design of novel therapeutic approaches for prevention and treatment of human cancers and other diseases. ..
- Control of SnoN Activity by SUMO modificationXia Lin; Fiscal Year: 2006..Finally, the results may also provide a foundation for the rational design of novel therapeutic approaches for prevention and treatment of cancer and musculoskeletal diseases. ..
