TY - JOUR
T1 - Nuclear organization and dynamics of 7SK RNA in regulating gene expression
AU - Prasanth, Kannanganattu V.
AU - Camiolo, Matthew
AU - Chan, Grace
AU - Tripathi, Vidisha
AU - Denis, Laurence
AU - Nakamura, Tetsuya
AU - Hübner, Michael R.
AU - Spector, David L.
PY - 2010/12/1
Y1 - 2010/12/1
N2 - 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.
AB - 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.
UR - http://www.scopus.com/inward/record.url?scp=78650084265&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=78650084265&partnerID=8YFLogxK
U2 - 10.1091/mbc.E10-02-0105
DO - 10.1091/mbc.E10-02-0105
M3 - Article
C2 - 20881057
AN - SCOPUS:78650084265
SN - 1059-1524
VL - 21
SP - 4184
EP - 4196
JO - Molecular biology of the cell
JF - Molecular biology of the cell
IS - 23
ER -