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SWI/SNF complex

Pereira LA, Bentley K, Peelers A, ChurchiU MJ, Deacon NJ (2000) A compilation of cellular transcription factor interactions with the HIV-1 LTR promoter. Nucleic Acids Res 28(3) 663-668 Persaud D, Zhou Y, Siliciano JM, Siliciano RF (2003) Latency in human immunodeficiency virus type 1 infection no easy answers. J Virol 77(3) 1659-1665 Peterson CL, Tamkun JW (1995) The SWI-SNF complex a chromatin remodeling machine Trends Biochem Sci 20(4) 143-146... [Pg.115]

Several links have emerged between remodelling factors and oncogenesis (reviewed in Cairns, 2001). Subunits of the mammalian SWI/SNF complex possess intrinsic tumour suppressor function or are required for the activity of other... [Pg.33]

Pray-Grant MG, Daniel JA, Schieltz D, Yates JR, 3rd, Grant PA (2005) Chdl chromodomain links histone H3 methylation with SAGA- and SLlK-dependent acetylation. Nature 433 434-438 Rando OJ, Zhao K, Janmey P, Crabtree GR (2002) Phosphatidylinositol-dependent actin filament binding by the SWI/SNF-hke BAF chromatin remodehng complex. Proc Natl Acad Sci USA 99 2824-2829 Roberts CW, Orkin SH (2004) The SWI/SNF complex - chromatin and cancer. Nat Rev Cancer 4 133-142... [Pg.43]

Whitehouse 1, Stockdale C, Haus A, Szczelkun MD, Owen-Hughes T (2003) Evidence for DNA translocation by the ISWl chromatin-remodeling enzyme. Mol Cell Biol 23 1935—1945 Wong AK, Shanahan E, Chen Y, Lian L, Ha P, Hendricks K, Ghaffari S, lliev D, Penn B, Woodland AM et al (2000) BRG1, a component of the SWI-SNF complex, is mutated in multiple human mmor cell lines. Cancer Res 60 6171—6177... [Pg.44]

Martens JA, Winston E (2003) Recent advances in understanding chromatin remodeling by Swi/Snf complexes. Curr Opin Genet Dev 13 136-142... [Pg.142]

Peterson CL, Workman JL (2000) Promoter targeting and chromatin remodeling by the SWI/SNF complex. Curr Opin Genet Dev 10 187-192... [Pg.394]

Bazett-Jones, D.P., Cote, J., Landel, C.C., Peterson, C.L., and Workman, J.L. (1999a) The SWI/ SNF complex creates loop domains in DNA and polynucleosome arrays and can disrupt DNA-histone contacts within these domains. Mol. Cell. Biol. 19(2), 1470-1478. [Pg.365]

S. cerevisiae 1000 molecules/cell. Chdlp is partially redundant with SWI/SNF complex, ISWlp and ISW2p [94,98]. Chdlp may function during transcript elongation [255]. [Pg.426]

More than one type of both the SWI/SNF and the ISWI polypeptides are found in most eukaryotic cells. Thus, the yeast representatives of the SWI/SNF complex are the SWI/SNF complex itself containing the Swi2p/Snf2p ATPase and the much more abundant RSC complex for which Sthlp is the ATPase subunit [35,77]. Both these complexes are very large ( 2 MDa) and contain 10-15 polypeptides [77-79]. Homologous assemblies are also found in vertebrates [80,81] BAF (otherwise known as hSwi/Snf-B) and PBAF (otherwise hSwi/Snf-A) being homologous to the yeast RSC and SWI/SNF complexes, respectively [82]. In addition, both the mammalian SWI/SNF and yeast RSC complexes can exist in functionally distinct forms [44,83,84]. [Pg.429]

Dallas, P.B., Pacchione, S., Wilsker, D., Bowrin, V., Kobayashi, R., and Moran, E. (2000) The human SWI-SNF complex protein p270 is an ARID family member with non-sequence-specific DNA binding activity. Mol. Cell. Biol. 20, 3137-3146. [Pg.456]

Aoyagi, S., Narlikar, G., Zheng, C., Sif, S., Kingston, R.E., and Hayes, J.J. (2002) Nucleosome remodeling by the human SWI/SNF complex requires transient global disruption of histone-DNA interactions. Mol. Cell. Biol. 22, 3653-3662. [Pg.457]


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See also in sourсe #XX -- [ Pg.8 ]




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