汤其群
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- 姓名:汤其群
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学术头衔:
博士生导师
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生物化学
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汤其群,教授,1990年上海医科大学法医系本科毕业,1995年获上海医科大学生物化学与分子生物学专业博士学位。1995-97年美国Johns Hopkins大学医学院生物化学系博士后,1997-2002年美国Johns Hopkins大学医学院生化系Faculty of Research Associate,2002年开始担任美国Johns Hopkins大学医学院儿科内分泌以及生化系助理教授。1999年获教育部“长江计划”特聘教授。现任复旦大学医学院教授,教育部分子医学重点实验室主任。曾承担国家重点攻关和上海市重点攻关项目各一个,均及时圆满完成,并因此获奖两次。现承担国家自然科学基金一项,国家“863”项目二项,高等学校骨干教师资助计划1项,上海市重大课题1项,重点课题3项,重点实验室合作开放基金1项。在研究生期间出色完成了基因工程链激酶(r-Sk)和基因工程葡激酶(r-Sak)的研制工作,为我国第一个有自主知识产权的一类生物技术新药r-Sk的研制和开发奠定了基础。作为主要完成人获国家科技进步二等奖,卫生部科技进步一等奖,上海市科技进步一等奖,中国专利金奖一项。还获得过“霍英东优秀青年教师”一等奖。近十年来主要从事脂肪细胞发育分化的分子机理研究,共发表SCI论文20篇,包括GENE&DEVELOPMENT、MCB、 PNAS等,他引384次。
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【期刊论文】Repressive Effect of Sp1 on the C/EBPα Gene Promoter: Role in Adipocyte Differentiation
汤其群, QI-QUN TANG, MAN-SHIOW JIANG, AND M. DANIEL LANE*
MOLECULAR AND CELLULAR BIOLOGY July 1999 p. 4855-4865,-0001,():
-1年11月30日
Expression of C/EBPα is required for differentiation of 3T3-L1 preadipocytes into adipocytes. Previous investigations indicated that transcription of the C/EBPα gene is sequentially activated during differentiation, initially by C/EBPβ and C/EBPδ and later by C/EBPα (autoactivation). These events are mediated by a C/EBP regulatory element in the promoter of the C/EBPα gene. This article presents evidence that members of the Sp family, notably Sp1, act repressively on the C/EBPα promoter prior to the induction of differentiation. Sp1 was shown to bind to a GC box at the 5' end of the C/EBP regulatory element in the C/EBPα promoter and, in so doing, to competitively prevent binding to and transactivation of the promoter by the C/EBPs. One of the differentiation inducers methylisobutylxanthine (a cAMP phosphodiesterase inhibitor) or Forskolin, both of which increase the cellular cAMP level, causes down-regulation of Sp1. This decrease in Sp1 level early in the differentiation program appears to facilitate access of C/EBPβ and/or C/EBPδ to the C/EBP regulatory element and, thereby, derepression of the C/EBPα gene.
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【期刊论文】Derepression of the C/EBPα gene during adipogenesis: Identification of AP-2α as a repressor
汤其群, MAN-SHIOW JIANG, QI-QUN TANG, JOHN MCLENITHAN, DEB GEIMAN, WENDY SHILLINGLAW*, WILLIAM J. HENZEL*, AND M. DANIEL LANE†
Proc. Natl. Acad. Sci. USA Vol. 95, pp. 3467-3471, March 1998 Biochemistry,-0001,():
-1年11月30日
ABSTRACT During adipogenesis, CCAAT/enhancer binding protein α(C/EBPα) serves as a pleiotropic transcriptional activator of adipocyte genes. Previously, we identified dual repressive elements in the C/EBPα gene and a putative transacting factor (C/EBPα undifferentiated protein, or CUP) expressed by preadipocytes, but not adipocytes, that bind to these elements. In the present investigation, CUP was purified 17,000-fold from nuclear extracts of 3T3-L1 preadipocytes. Amino acid sequence and mass spectral analysis of tryptic peptides derived from purifed CUP (molecular mass '50 kDa) revealed that the repressor is (or contains) an isoform of the transcription factor, AP-2α. Electrophoretic mobility shift and Western blot analysis on purified CUP and preadipocyte nuclear extracts confirmed the identity of CUP as AP-2α. Both AP-2α protein and CUP binding activity are expressed by preadipocytes and then decrease concomitantly during differentiation of 3T3-L1 preadipocytes into adipocytes. Consistent with a repressive role of AP-2α/CUP, an AP-2α1 expression vector, cotransfected with a C/EBPα promoter-reporter construct into 3T3-L1 adipocytes, inhibited reporter gene transcription. Taken together with previous results, these findings suggest that in preadipocytes the C/EBPα gene is repressed by AP-2α/CUP, which, upon induction of differentiation, is down-regulated, allowing expression of the gene.
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【期刊论文】CCAAT/enhancer-binding proteinβ is required for mitotic clonal expansion during adipogenesis
汤其群, Qi-Qun Tang*†‡, Tamara C. Otto*, and M. Daniel Lane*
PNAS February 4, 2003 vol. 100 no.3 853,-0001,():
-1年11月30日
Hormonal induction of growth-arrested 3T3-L1 preadipocytes triggers a signaling cascade that culminates in adipogenesis. CCAAT/enhancer-binding protein (C/EBP)β is expressed immediately but gains DNA-binding activity only after a long lag as the cells synchronously begin mitotic clonal expansion (MCE). After MCE, a process required for adipogenesis, C/EBP activates expression of C/EBPα and peroxisome proliferator-activated receptorγ, which then transcriptionally activate genes that produce the adipocyte phenotype. When mouse embryo fibroblasts (MEFs) are subjected to the same differentiation protocol, a subset of the MEFs undergoes a similar program of events. Similar to 3T3-L1 preadipocytes, the MEFs reenter the cell cycle (as indicated by the synchronous expression of cyclin A) and undergo MCE as evidenced by the incorporation of BrdUrd into DNA and the formation of mitotic foci of cells that undergo adipogenesis. C/EBPβ is expressed immediately after induction but exhibits delayed acquisition of DNAbinding activity followed by expression of adipocyte markers and the accumulation of cytoplasmic triglyceride. MEFs from C/EBPβ (-/-) mice, however, neither undergo MCE nor differentiate into adipocytes. Forced expression of C EBP (LAP) but not dominant-negative C/EBPβ (LIP) in C/EBPβ (-/-) MEFs restores MCE, expression of adipocyte markers, and the capacity to form mitotic foci of cells that undergo adipogenesis. These findings demonstrate that expression of C/EBPβ is a prerequisite for MCE in the adipocyte-differentiation program.
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汤其群, Frederick Y. Wu*†, Qi-Qun Tang‡§, Honglin Chen†, Colette ApRhys†, Christopher Farrell*, Jianmeng Chen*, Masahiro Fujimuro†, M. Daniel Lane‡, and Gary S. Hayward*†¶
PNAS August 6, 2002 vol. 99 no.16 10687,-0001,():
-1年11月30日
Kaposi sarcoma-associated herpesvirus (KSHV) is an oncogenic DNA virus that causes Kaposi sarcoma and AIDS-related primary effusion lymphoma (PEL). Here we show that KSHV lytic cycle replication in PEL cells induces G1 cell cycle arrest, presumably to facilitate the progression of viral DNA replication. Expression of a KSHV-encoded early lytic protein referred to as RAP or K8 is induced within 12-2h after the onset of lytic cycle induction in host PEL cells, and coincides with increased levels of both the endogenous C/EBPα and p21CIP-1 proteins in the nucleus of the same cells. The KSHV RAP protein binds to C/EBPα in vitro and stimulates C/EBPα-induced expression from both the C/EBPα and p21 promoters in cotransfected cells. A recombinant adenovirus expressing the RAP protein induced the expression of both the C/EBPα and p21 proteins in primary human fibroblasts, and flow cytometric analysis revealed a dramatic inhibition of G1 to S cell cycle progression in the same cells. All of these effects were abolished in cells that lack C/EBPα or by deletion of the basic leucine zipper region in RAP that interacts with C/EBPα. Therefore, C/EBPα is essential for the p21-mediated inhibition of G1 to S-phase progression by RAP in KSHV-infected host cells.
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汤其群, Qi-Qun Tang and M. Daniel Lane
GENES & DEVELOPMENT 13: 2231-2241,-0001,():
-1年11月30日
Hormonal induction of 3T3-L1 preadipocytes triggers a cascade of events that initiate differentiation into adipocytes. CCAAT/enhancer-binding proteinsβ andδ (C/EBPβ/δ) are expressed early in the differentiation program, but are not immediately active. After a long lag, C/EBPβ/δ become competent to bind to the C/EBP regulatory element in the C/EBPa gene promoter, C/EBPa being a transcriptional activator of numerous adipocyte genes. As C/EBPβ/δ acquire binding activity, they become localized to centromeres as preadipocytes synchronously enter S phase at the onset of mitotic clonal expansion. Localization to centromeres occurs through C/EBP consensus-binding sites in centromeric satellite DNA. C/EBPa, which is antimitotic, becomes centromere-associated much later in the differentiation program as mitotic clonal expansion ceases and the cells become terminally differentiated.
3T3-L1 preadipocyte, cell cycle, C/, EBP, satellite DNA, centromere
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汤其群, Qi-Qun Tang* and M. Daniel Lane
PNAS November 7, 2000 vol. 97 no.23 12449,-0001,():
-1年11月30日
Hormone induction of growth-arrested preadipocytes triggers mitotic clonal expansion followed by expression of CCAAT/enhancer- binding protein (C/EBP)α and differentiation into adipocytes. The order of these events is critical because C/EBPα is antimitotic and its expression prematurely would block the mitotic clonal expansion required for differentiation. C/EBPβ, a transcriptional activator of the C/EBPα gene, is expressed early in the differentiation program, but lacks DNA-binding activity and fails to localize to centromeres until preadipocytes traverse the G1-S checkpoint of mitotic clonal expansion. Evidence is presented that dominantnegative CHOP-10 expressed by growth-arrested preadipocytes transiently sequesters C/EBPβ by heterodimerization. As preadipocytes reach S phase, CHOP-10 is down-regulated, apparently releasing C/EBPβ from inhibitory constraint and allowing transactivation of the C/EBPα gene. In support of these findings, up-regulation of CHOP-10 with the protease inhibitor N-acetyl-Leu-Leu-norleucinal prevents activation of C/EBPβ, expression of C/EBPα, and adipogenesis.
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汤其群, QI-QUN TANG, MAN-SHIOW JIANG, AND M. DANIEL LANE†
Proc. Natl. Acad. Sci. USA Vol. 94, pp. 13571-13575, December 1997 Biochemistry,-0001,():
-1年11月30日
ABSTRACT During adipocyte differentiation, the expression of CyEBPα is activated, which in turn serves to transcriptionally activate numerous adipocyte genes. A previous search for cis elements that regulate transcription of the CyEBPagene led to the identification of a potential repressive element within the proximal 5' flanking region of the gene. Nuclear extracts from 3T3-L1 preadipocytes, but not adipocytes, were found to contain a factor, CUP (C/EBPα undifferentiated protein), that binds to this site (the CUP-1 site). In the present investigation, we show that C/EBPα promoterluciferase constructs containing both the proximal 5' flanking and the entire 5' untranslated regions of the gene exhibit an expression pattern during adipocyte differentiation comparable to that of the endogenous C/EBPα gene. Mutation of the CUP-1 site in these constructs had little effect on reporter gene expression; however, when this mutation was combined with deletion of the 5' untranslated region, reporter gene expression by preadipocytes was dramatically up-regulated. Consistent with this finding, a second CUP binding site (the CUP-2 site) was identified in the 5' untranslated region. Although mutation of either CUP element in constructs containing both the 5' flanking and 5' untranslated region had little effect on reporter gene transcription, mutation of both CUP elements markedly activated transcription. Thus, it appears that dual CUP regulatory elements repress transcription of the C/EBPa gene prior to induction of the adipocyte differentiation program.
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【期刊论文】Mitotic clonal expansion: A synchronous process required for adipogenesis
汤其群, Qi-Qun Tang*†‡, Tamara C. Otto*, and M. Daniel Lane*
PNAS January 7, 2003 vol. 100 no.1 49,-0001,():
-1年11月30日
When induced to differentiate, growth-arrested 3T3-L1 preadipocytes synchronously reenter the cell cycle and undergo mitotic clonal expansion (MCE) followed by expression of genes that produce the adipocyte phenotype. The preadipocytes traverse the G1/S checkpoint synchronously as evidenced by the expression activation of cdk2-cyclin-E/A, turnover of p27 kip1, hyperphosphorylation of Rb, translocation of cyclin D1 from nuclei to cytoplasm and GSK-3β from cytoplasm to nuclei, and incorporation of [3H] thymidine into DNA. As the cells cross the G1/S checkpoint, C/EBPβ acquires DNA-binding activity, initiating a cascade of transcriptional activation that culminates in the expression of adipocyte proteins. The mitogen-activated protein kinase extracellular signal-regulated kinase kinase (MEK) inhibitor PD98059 delays, but does not block, MCE and differentiation, the extent of the delay causing a comparable delay in the expression of cell-cycle markers, MCE, and adipogenesis. The more potent and specific MEK inhibitor UO126 and the cyclin-dependent kinase inhibitor roscovitine, which inhibit the cell cycle at different points, block MCE, expression of cell cycle and adipocyte markers, as well as adipogenesis. These results show that MCE is a prerequisite for differentiation of 3T3-L1 preadipocytes into adipocytes.
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