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A strong internal promoter drives massive expression of YEATS-domain devoid MLLT3 transcripts in HSC and most lethal AML
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作者 ChloéBessière Ahmed Zamani +12 位作者 Romain Pfeifer Sandra Dailhau Camille Marchet Benoit Guibert Anthony Boureux Raissa Silva Da Silva Nicolas Gilbert Thérèse Commes Fabienne Meggetto Christian Touriol Christian Récher Marina Bousquet stéphane pyronnet 《Cancer Communications》 2025年第3期380-385,共6页
The AF9(protein AF9)transcription factor,encoded by MLLT3(mixed-lineage leukemia translocated to 3)on chromosome 9,functions as a chromatin reader.Through its N-terminal YEATS(Yaf9,ENL,AF9,Taf14,and Sas5)protein domai... The AF9(protein AF9)transcription factor,encoded by MLLT3(mixed-lineage leukemia translocated to 3)on chromosome 9,functions as a chromatin reader.Through its N-terminal YEATS(Yaf9,ENL,AF9,Taf14,and Sas5)protein domain,it interacts with acetylated[1]or crotonylated[2]histone H3,as well as with the PAF1(RNA polymerase II-associated factor 1 homolog)and P-TEFb(positive transcription elongation factor b)components of the super elongation complex(SEC).AF9 also interacts through its poly-serine domain(Poly-Ser)with the TFIID(Transcription factor II D)subunit of the RNA polymerase II(RNApol II)complex.In addition,its C-terminal transactivation domain,AHD(nuclear anchorage protein1 homology domain),binds other SEC components,such as AFF1 and AFF4(ALF transcription elongation factor 1 or 4),aswell as transcription regulators CBX8(chromobox 8),DOT1L(disruptor of telomeric silencing 1 like),and BCOR(B cell lymphoma 6 corepressor),as reviewed by Kabra&Bushweller[3](Figure 1A).Thus,MLLT3 is an integral part of the SEC,which is essential for optimizing the catalytic activity of RNApol II transcription at specific genome loci. 展开更多
关键词 chromatin reader Yeats domain Mixed lineage leukemia translocated chromatin readerthrough Transcription factor II D RNA polymerase II AF Poly serine domain
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