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ss18 together with animal-specific factors defines human baf-type swisnf complexesss18一起种只感染动物的因素定义了人类baf-type swisnf复合物.pdfVIP

ss18 together with animal-specific factors defines human baf-type swisnf complexesss18一起种只感染动物的因素定义了人类baf-type swisnf复合物.pdf

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ss18 together with animal-specific factors defines human baf-type swisnf complexesss18一起种只感染动物的因素定义了人类baf-type swisnf复合物

SS18 Together with Animal-Specific Factors Defines Human BAF-Type SWI/SNF Complexes ¤ Evelien Middeljans, Xi Wan, Pascal W. Jansen , Vikram Sharma, Hendrik G. Stunnenberg, Colin Logie* Department of Molecular Biology, Nijmegen Centre for Molecular Life Sciences, Radboud University, Nijmegen, The Netherlands Abstract Background: Nucleosome translocation along DNA is catalyzed by eukaryotic SNF2-type ATPases. One class of SNF2- ATPases is distinguished by the presence of a C-terminal bromodomain and is conserved from yeast to man and plants. This class of SNF2 enzymes forms rather large protein complexes that are collectively called SWI/SNF complexes. They are involved in transcription and DNA repair. Two broad types of SWI/SNF complexes have been reported in the literature; PBAF and BAF. These are distinguished by the inclusion or not of polybromo and several ARID subunits. Here we investigated human SS18, a protein that is conserved in plants and animals. SS18 is a putative SWI/SNF subunit which has been implicated in the etiology of synovial sarcomas by virtue of being a target for oncogenic chromosomal translocations that underlie synovial sarcomas. Methodology/Principal Findings: We pursued a proteomic approach whereby the SS18 open reading frame was fused to a tandem affinity purification tag and expressed in amenable human cells. The fusion permitted efficient and exclusive purification of so-called BAF-type SWI/SNF complexes which bear ARID1A/BAF250a or ARID1B/BAF250b subunits. This demonstrates that SS18 is a BAF subtype-specific SWI/SNF complex subunit. The same result was obtained when using the SS18-SSX1 oncogenic translocation product. Furthermore, SS18L1, DPF1, DPF2, DPF3, BRD9, BCL7A, BCL7B and BCL7C were identi

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