• Documents
  • Authors
  • Tables
  • Log in
  • Sign up
  • MetaCart
  • DMCA
  • Donate

CiteSeerX logo

Advanced Search Include Citations
Advanced Search Include Citations

Functional interactions between the hBRM/hBRG1 transcriptional activators and the pRB family of proteins. (1996)

by B E Strober, J L Dunaief, Goff Guha, S P
Venue:Mol. Cell. Biol.
Add To MetaCart

Tools

Sorted by:
Results 1 - 10 of 29
Next 10 →

Transcription activator interactions with multiple SWI/SNF subunits

by Kristen E. Neely, Ahmed H. Hassan, Christine E. Brown, Leann Howe, Jerry L. Workman, Kristen E. Neely, Ahmed H. Hassan, Christine E. Brown, Leann Howe, Jerry L. Workman , 2002
"... These include: This article cites 73 articles, 38 of which can be accessed free at: ..."
Abstract - Cited by 43 (2 self) - Add to MetaCart
These include: This article cites 73 articles, 38 of which can be accessed free at:
(Show Context)

Citation Context

...also been implicated as a tumor suppressor and as a target for mutation in human cancer (69). BRG1 is also an important regulator of cell growth through its interactions with the tumor suppressor pRb =-=(14, 55, 75)-=-. A BRG1-containing SWI/SNF complex was recently purified via association with the tumor suppressor and transcriptional regulator BRCA1 through a direct interaction between BRG1 and BRCA1 (4). Our exp...

Mammalian SWI-SNF complexes contribute to activation of the hsp70

by Ivana L. De La Serna, Kerri A. Carlson, David A. Hill, J. Guidi, Ryan O. Stephenson, Saïd Sif, Robert E. Kingston, Anthony N. Imbalzano, Ivana L. De La Serna, Kerri A. Carlson, David A. Hill, Cynthia J. Guidi, Ryan O. Stephenson, Saïd Sif, Robert E. Kingston, Anthony N. Imbalzano , 2000
"... This article cites 92 articles, 43 of which can be accessed free at: ..."
Abstract - Cited by 28 (10 self) - Add to MetaCart
This article cites 92 articles, 43 of which can be accessed free at:
(Show Context)

Citation Context

...h, and development and differentiation (reviewed in reference 23). Regulation of cell cycle progression may occur via interaction of BRG1-hBRM with the retinoblastoma oncoprotein (Rb) and/or cyclin E =-=(14, 62, 65, 69)-=-. In addition, the complex or individual subunits may be targeted by viral regulatory proteins upon infection of cells by adenovirus, EpsteinBarr virus, human papillomavirus, and human immunodeficienc...

Prohibitin facilitates cellular senescence by recruiting specific corepressors to inhibit E2F target genes. Mol Cell Biol 2006

by Shipra Rastogi, Bharat Joshi, Piyali Dasgupta, Mark Morris, Kenneth Wright
"... Prohibitin is a growth regulatory gene that has pleiotropic functions in the nucleus, mitochondria, and cytoplasmic compartments. Earlier studies had proposed a role for prohibitin in modulating cellular senes-cence, but the underlying mechanisms remain unknown. Here we show that senescence induced ..."
Abstract - Cited by 12 (2 self) - Add to MetaCart
Prohibitin is a growth regulatory gene that has pleiotropic functions in the nucleus, mitochondria, and cytoplasmic compartments. Earlier studies had proposed a role for prohibitin in modulating cellular senes-cence, but the underlying mechanisms remain unknown. Here we show that senescence induced by DNA-damaging agents causes the localization of prohibitin to specific heterochromatic foci. Prohibitin could bind to heterochromatin protein 1 (HP1) family proteins and colocalized with HP1 in senescence-associated hetero-chromatic foci. Further, HP1 could synergize with prohibitin to repress E2F1-mediated transcriptional activity. The depletion of prohibitin by small interfering RNA or antisense techniques led to a reduction in the senescent phenotype, correlating with a reduced expression of senescence-associated -galactosidase and fewer numbers of senescence-associated heterochromatic foci. Chromatin immunoprecipitation assays showed that prohibitin is needed for the recruitment of HP1 to E2F1-regulated proliferative promoters, leading to their repression. The ablation of prohibitin prevented the recruitment of HPI, but not Suv39H, to the promoters upon senescence. Prohibitin-mediated recruitment of HP1 occurred in only senescent cells, not in quiescent cells; thus, there is a dichotomy in the recruitment of different corepressors by prohibitin, depending on the type of growth arrest. These studies show that prohibitin plays a vital role in inducing cellular senescence. Primary mammalian cells in culture undergo a period of
(Show Context)

Citation Context

...ssors, including histone deacetylase 1 (HDAC1), DNA methyltransferase, and Polycomb proteins as well as chromatin-remodeling complexes like Brg and Brm, to repress the transcriptional activity of E2F =-=(4, 32, 33, 35, 48, 58, 61, 62, 66)-=-. Rb has been shown to associate with HP1 and histone methyltransferase Suv39H to facilitate senescence (28, 37, 60). This facilitation is achieved by accumulating on E2Fresponsive proliferative promo...

Role for BRG1 in cell cycle control and tumor suppression

by Kristin B. Hendricks, Frances Shanahan, Emma Lees, Updated Information, Kristin B. Hendricks, Frances Shanahan, Emma Lees - Mol. Cell. Biol , 2004
"... This article cites 62 articles, 30 of which can be accessed free ..."
Abstract - Cited by 11 (0 self) - Add to MetaCart
This article cites 62 articles, 30 of which can be accessed free
(Show Context)

Citation Context

...complex, the ATPase activity being generated by BRG1, a 190-kDa component, or a related protein, hBRM (58). In mammalian cells BRG1 is known to play a role in the regulation of cellular proliferation =-=(8, 49)-=-. This activity of BRG1 has been shown to be dependent on its association with the retinoblastoma tumor suppressor gene product (pRB) and, consequently, via the repression of E2F target gene expressio...

The activity of mammalian brm/SNF2� is dependent on a high-mobility-group protein I/Y-like DNA binding domain

by Brigitte Bourachot, Moshe Yaniv, Christian Muchardt, Mol Cell Biol, Brigitte Bourachot, Moshe Yaniv, Christian Muchardt , 1999
"... These include: This article cites 61 articles, 21 of which can be accessed free at: ..."
Abstract - Cited by 8 (0 self) - Add to MetaCart
These include: This article cites 61 articles, 21 of which can be accessed free at:
(Show Context)

Citation Context

... simian virus 40 large T antigen. In addition, the brm and BRG-1 proteins, when transiently transfected in SW13 cells, can cooperate with p105 Rb to induce the formation of flat, growtharrested cells =-=(12, 43, 47)-=-. Cotransfection studies also show a cooperation between brm and p105 Rb for the repression of E2F-activated transcription (50). Consistent with these observations, the brm protein was found to accumu...

The BRG1- and hBRM-Associated Factor BAF57 Induces Apoptosis by Stimulating Expression of the Cylindromatosis Tumor Suppressor Gene†

by Li Wang, Robert A. Baiocchi, Sharmistha Pal, Michael Caligiuri, Saïd Sif, Li Wang, Robert A. Baiocchi, Sharmistha Pal, George Mosialos, Michael Caligiuri, Saïd Sif , 2005
"... This article cites 52 articles, 21 of which can be accessed free ..."
Abstract - Cited by 7 (2 self) - Add to MetaCart
This article cites 52 articles, 21 of which can be accessed free
(Show Context)

Citation Context

...r proteins lends further support to the notion that BRG1- and hBRM-based hSWI/SNF complexes affect cell growth and proliferation by interacting with and probably controlling tumor suppressor pathways =-=(6, 8, 13, 18, 43, 46, 52)-=-. The BT549 cell line is an invasive human ductal epithelial breast cancer line that lacks expression of BAF57, which can bind DNA via its high-mobility group-like domain and mediate interaction with ...

Adenovirus E1A specifically blocks SWI/SNFdependent transcriptional activation

by Mary E. Miller, Bradley R. Cairns, Randy S. Levinson, Keith R. Yamamoto, Daniel A. Engel, M. Mitchell Smith , 1996
"... Expression of the adenovirus E1A243 oncoprotein in Saccharomyces cerevisiae produces a slow-growth phe-notype with accumulation of cells in the G1 phase of the cell cycle. This effect is due to the N-terminal and CR1 domains of E1A243, which in rodent cells are involved in triggering cellular transf ..."
Abstract - Cited by 5 (1 self) - Add to MetaCart
Expression of the adenovirus E1A243 oncoprotein in Saccharomyces cerevisiae produces a slow-growth phe-notype with accumulation of cells in the G1 phase of the cell cycle. This effect is due to the N-terminal and CR1 domains of E1A243, which in rodent cells are involved in triggering cellular transformation and also in binding to the cellular transcriptional coactivator p300. A genetic screen was undertaken to identify genes required for the function of E1A243 in S. cerevisiae. This screen identified SNF12, a gene encoding the 73-kDa subunit of the SWI/SNF transcriptional regulatory complex. Mutation of genes encoding known members of the SWI/SNF complex also led to loss of E1A function, suggesting that the SWI/SNF complex is a target of E1A243. Moreover, expression of E1A in wild-type cells specifically blocked transcriptional activation of the INO1 and SUC2 genes, whose activation pathways are distinct but have a common requirement for the SWI/SNF complex. These data demonstrate a specific functional interaction between E1A and the SWI/SNF complex and suggest that a similar interaction takes place in rodent and human cells. The adenovirus E1A gene encodes potent oncoproteins that function as regulators of cellular and viral transcription. In the context of a normal adenovirus replicative cycle in permissive human hosts, the E1A proteins perform two main functions.
(Show Context)

Citation Context

... yeast SNF2 (8). A connection between E1A and mammalian SWI/SNF is also suggested by the fact that Rb, itself a target of E1A, can physically interact with hBRG1 and hBRM, a second human SNF2 homolog =-=(12, 53)-=-. Therefore, E1A may have evolved to alter mammalian SWI/SNF function in more than one way. In S. cerevisiae, E1A may bind directly to a specific member of the SWI/SNF complex, a homolog of p300, or a...

Nucleocytoplasmic Shuttling of p130/RBL2: Novel Regulatory Mechanism

by Anton Chestukhin, Larisa Litovchick, Katherine Rudich, James A. Decaprio, Updated Information, Anton Chestukhin, Larisa Litovchick, Katherine Rudich, James A. Decaprio , 2001
"... These include: This article cites 87 articles, 53 of which can be accessed free at: ..."
Abstract - Cited by 4 (0 self) - Add to MetaCart
These include: This article cites 87 articles, 53 of which can be accessed free at:
(Show Context)

Citation Context

... including adenovirus E1A, simian virus 40 (SV40) large T antigen (T-Ag), and human papillomavirus E7 (18, 23, 81), as well as cellular proteins such as histone deacetylase 1 and 2 (5, 50), BRG1, BRM =-=(22, 73, 76)-=-, and others (20). The ability of the LXCXE motif of viral oncoproteins to interact with pRb family members is indispensable for virus-mediated transformation (9, 74, 83, 88, 89). However, pRb mutants...

Regulation of cellular genes in a chromosomal context by the retinoblastoma tumor suppressor protein

by Ann Marie Buchmann, Sathyamangalam Swaminathan, Mol Cell Biol, Ann Marie Buchmann, Sathyamangalam Swaminathan , 1998
"... These include: This article cites 63 articles, 37 of which can be accessed free at: ..."
Abstract - Cited by 3 (0 self) - Add to MetaCart
These include: This article cites 63 articles, 37 of which can be accessed free at:
(Show Context)

Citation Context

...eviewed in reference 55). pRb binds two of these proteins, hBRM and hBRG1, and overexpression of these proteins produces a growth suppression phenotype similar to that seen with overexpression of pRb =-=(47)-=-. Thus, it is likely that transcriptional control by pRb is greatly influenced by promoter structure. Our own experiments have seen discrepancies in transcriptional regulation between transient-transf...

ATP-Dependent Chromatin-Remodeling Complexes

by Doi:mol Cell Biol, Jerry L. Workman, Marissa Vignali, Ahmed H. Hassan, Kristen E. Neely, Marissa Vignali, Ahmed H. Hassan, Kristen E. Neely, Jerry, L. Workman
"... This article cites 126 articles, 56 of which can be accessed free ..."
Abstract - Cited by 3 (0 self) - Add to MetaCart
This article cites 126 articles, 56 of which can be accessed free
(Show Context)

Citation Context

...s, can physically interact with Rb. Furthermore, these studies showed that hBRG1/hBRM can function as tumor suppressor genes and induce the formation of growth-arrested cells in an Rbdependent manner =-=(24, 99)-=-. Rb has a central role in the control of fundamental cellular processes such as proliferation and differentiation. Therefore, these studies suggest that the ATPase subunits of hSWI/SNF complexes coop...

Powered by: Apache Solr
  • About CiteSeerX
  • Submit and Index Documents
  • Privacy Policy
  • Help
  • Data
  • Source
  • Contact Us

Developed at and hosted by The College of Information Sciences and Technology

© 2007-2019 The Pennsylvania State University