Nuclear Organization and Dynamics of 7SK RNA in Regulating Gene Expression

Author:

Prasanth Kannanganattu V.1,Camiolo Matthew1,Chan Grace1,Tripathi Vidisha2,Denis Laurence1,Nakamura Tetsuya13,Hübner Michael R.1,Spector David L.1

Affiliation:

1. Cold Spring Harbor Laboratory, Cold Spring Harbor, NY, 11724;

2. Department of Cell and Developmental Biology, University of Illinois at Urbana-Champaign, Urbana, IL 61801;

3. Department of Gasteroenterology and Hepatology, Tokyo Medical and Dental University, 1-5-45, Yushima Bunkyo-ku, Tokyo 113-8519

Abstract

Noncoding RNAs play important roles in various aspects of gene regulation. We have identified 7SK RNA to be enriched in nuclear speckles or interchromatin granule clusters (IGCs), a subnuclear domain enriched in pre-mRNA processing factors. 7SK RNA, in association with HEXIM 1 and 2, is involved in the inhibition of transcriptional elongation by RNA polymerase II. Inhibition occurs via sequestration of the active P-TEFb kinase complex (CDK 9 and Cyclin T1/T2a/b or K) that is involved in phosphorylating the C-terminal domain of RNA polymerase II. Our results demonstrate that knock-down of 7SK RNA, by specific antisense oligonucleotides, results in the mislocalization of nuclear speckle constituents in a transcription-dependent manner, and the transcriptional up-regulation of a RNA polymerase II transcribed reporter gene locus. Furthermore, 7SK RNA transiently associates with a stably integrated reporter gene locus upon transcriptional down-regulation and its presence correlates with the efficient displacement of P-TEFb constituents from the locus. Our results suggest that 7SK RNA plays a role in modulating the available level of P-TEFb upon transcriptional down-regulation by sequestering its constituents in nuclear speckles.

Publisher

American Society for Cell Biology (ASCB)

Subject

Cell Biology,Molecular Biology

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