7SK small nuclear RNA directly affects HMGA1 function in transcription regulation

被引:45
作者
Eilebrecht, Sebastian [1 ,2 ]
Brysbaert, Guillaume [1 ,2 ]
Wegert, Thomas [3 ]
Urlaub, Henning [4 ]
Benecke, Bernd-Joachim [3 ]
Benecke, Arndt [1 ,2 ]
机构
[1] Inst Hautes Etud Sci, F-91440 Bures Sur Yvette, France
[2] Ctr Natl Rech Sci USR3078, F-91440 Bures Sur Yvette, France
[3] Ruhr Univ Bochum, Dept Biochem, D-44780 Bochum, Germany
[4] Max Planck Inst Biophys Chem, Dept Cellular Biochem, Bioanalyt Mass Spectrometry Grp, D-37077 Gottingen, Germany
关键词
FACTOR P-TEFB; POLYMERASE-II TRANSCRIPTION; NONCODING RNAS; THERAPEUTIC STRATEGIES; GENE-EXPRESSION; BINDING DOMAIN; HIV-1; TAT; PROTEINS; ELONGATION; CHROMATIN;
D O I
10.1093/nar/gkq1153
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Non-coding (nc) RNAs are increasingly recognized to play important regulatory roles in eukaryotic gene expression. The highly abundant and essential 7SK ncRNA has been shown to negatively regulate RNA Polymerase II transcription by inactivating the positive transcription elongation factor b (P-TEFb) in cellular and Tat-dependent HIV transcription. Here, we identify a more general, P-TEFb-independent role of 7SK RNA in directly affecting the function of the architectural transcription factor and chromatin regulator HMGA1. An important regulatory role of 7SK RNA in HMGA1-dependent cell differentiation and proliferation regulation is uncovered with the identification of over 1500 7SK-responsive HMGA1 target genes. Elevated HMGA1 expression is observed in nearly every type of cancer making the use of a 7SK substructure in the inhibition of HMGA1 activity, as pioneered here, potentially useful in therapy. The 7SK-HMGA1 interaction not only adds an essential facet to the comprehension of transcriptional plasticity at the coupling of initiation and elongation, but also might provide a molecular link between HIV reprogramming of cellular gene expression-associated oncogenesis.
引用
收藏
页码:2057 / 2072
页数:16
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