7SK RNA: Difference between revisions

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In [[molecular biology]] '''7SK''' is an abundant small nuclear RNA found in [[metazoa]]ns.<ref>{{cite journal | vauthors = Diribarne G, Bensaude O | title = 7SK RNA, a non-coding RNA regulating P-TEFb, a general transcription factor | journal = RNA Biology | volume = 6 | issue = 2 | pages = 122–8 | year = 2009 | pmid = 19246988 | url = http://www.landesbioscience.com/journals/rnabiology/article/8115/?nocache=926590083 }}</ref>  It plays a role in regulating transcription by controlling the positive transcription elongation factor [[P-TEFb]].<ref name="Peterlin">{{cite journal | vauthors = Peterlin BM, Brogie JE, Price DH | title = 7SK snRNA: a noncoding RNA that plays a major role in regulating eukaryotic transcription | journal = Wiley Interdisciplinary Reviews. RNA | volume = 3 | issue = 1 | pages = 92–103 | year = 2012 | pmid = 21853533 | pmc = 3223291 | doi = 10.1002/wrna.106 | url = http://onlinelibrary.wiley.com/doi/10.1002/wrna.106/pdf }}</ref> 7SK is found in a [[Small Nuclear Ribonucleoprotein Particles|small nuclear ribonucleoprotein complex]] (snRNP) with a number of other proteins that regulate the stability and function of the complex.
In [[molecular biology]] '''7SK''' is an abundant small nuclear RNA found in [[metazoa]]ns.<ref>{{cite journal | vauthors = Diribarne G, Bensaude O | title = 7SK RNA, a non-coding RNA regulating P-TEFb, a general transcription factor | journal = RNA Biology | volume = 6 | issue = 2 | pages = 122–8 | year = 2009 | pmid = 19246988 | url = http://www.landesbioscience.com/journals/rnabiology/article/8115/?nocache=926590083 | doi=10.4161/rna.6.2.8115}}</ref>  It plays a role in regulating transcription by controlling the positive transcription elongation factor [[P-TEFb]].<ref name="Peterlin">{{cite journal | vauthors = Peterlin BM, Brogie JE, Price DH | title = 7SK snRNA: a noncoding RNA that plays a major role in regulating eukaryotic transcription | journal = Wiley Interdisciplinary Reviews: RNA | volume = 3 | issue = 1 | pages = 92–103 | year = 2012 | pmid = 21853533 | pmc = 3223291 | doi = 10.1002/wrna.106 | url = http://onlinelibrary.wiley.com/doi/10.1002/wrna.106/pdf }}</ref> 7SK is found in a [[Small Nuclear Ribonucleoprotein Particles|small nuclear ribonucleoprotein complex]] (snRNP) with a number of other proteins that regulate the stability and function of the complex.


==Structure ==
==Structure ==


An early study indicated that 7SK in cells is associated with a number of proteins and [[RNA structure probing|probing]] of the [[RNA structure|secondary structure]] suggested a model for [[base pair]]ing between different regions of the RNA.<ref>{{cite journal | vauthors = Wassarman DA, Steitz JA | title = Structural analyses of the 7SK ribonucleoprotein (RNP), the most abundant human small RNP of unknown function | journal = Molecular and Cellular Biology | volume = 11 | issue = 7 | pages = 3432–45 | date = July 1991 | pmid = 1646389 | pmc = 361072 | doi = 10.1128/MCB.11.7.3432 | url = http://mcb.asm.org/content/11/7/3432.long }}</ref> A breakthrough in the function of the 7SK snRNP came with the finding that the positive transcription elongation factor P-TEFb was a component of the complex.<ref>{{cite journal | vauthors = Nguyen VT, Kiss T, Michels AA, Bensaude O | title = 7SK small nuclear RNA binds to and inhibits the activity of CDK9/cyclin T complexes | journal = Nature | volume = 414 | issue = 6861 | pages = 322–5 | date = November 2001 | pmid = 11713533 | doi = 10.1038/35104581 | url = http://www.nature.com/nature/journal/v414/n6861/full/414322a0.html }}</ref><ref>{{cite journal | vauthors = Yang Z, Zhu Q, Luo K, Zhou Q | title = The 7SK small nuclear RNA inhibits the CDK9/cyclin T1 kinase to control transcription | journal = Nature | volume = 414 | issue = 6861 | pages = 317–22 | date = November 2001 | pmid = 11713532 | doi = 10.1038/35104575 | url = http://www.nature.com/nature/journal/v414/n6861/full/414317a0.html }}</ref> 7SK associates with and inhibits the cyclin dependent kinase activity of P-TEFb through the action of the RNA binding proteins [[HEXIM1]]<ref>{{cite journal | vauthors = Michels AA, Nguyen VT, Fraldi A, Labas V, Edwards M, Bonnet F, Lania L, Bensaude O | title = MAQ1 and 7SK RNA interact with CDK9/cyclin T complexes in a transcription-dependent manner | journal = Molecular and Cellular Biology | volume = 23 | issue = 14 | pages = 4859–69 | date = July 2003 | pmid = 12832472 | pmc = 162212 | doi = 10.1128/MCB.23.14.4859-4869.2003 | url = http://mcb.asm.org/content/23/14/4859.long }}</ref><ref>{{cite journal | vauthors = Yik JH, Chen R, Nishimura R, Jennings JL, Link AJ, Zhou Q | title = Inhibition of P-TEFb (CDK9/Cyclin T) kinase and RNA polymerase II transcription by the coordinated actions of HEXIM1 and 7SK snRNA | journal = Molecular Cell | volume = 12 | issue = 4 | pages = 971–82 | date = October 2003 | pmid = 14580347 | doi = 10.1016/S1097-2765(03)00388-5 | url = http://www.sciencedirect.com/science/article/pii/S1097276503003885 }}</ref> or [[HEXIM2]].<ref>{{cite journal | vauthors = Byers SA, Price JP, Cooper JJ, Li Q, Price DH | title = HEXIM2, a HEXIM1-related protein, regulates positive transcription elongation factor b through association with 7SK | journal = The Journal of Biological Chemistry | volume = 280 | issue = 16 | pages = 16360–7 | date = April 2005 | pmid = 15713662 | doi = 10.1074/jbc.M500424200 | url = http://www.jbc.org/content/280/16/16360.long }}</ref><ref>{{cite journal | vauthors = Yik JH, Chen R, Pezda AC, Zhou Q | title = Compensatory contributions of HEXIM1 and HEXIM2 in maintaining the balance of active and inactive positive transcription elongation factor b complexes for control of transcription | journal = The Journal of Biological Chemistry | volume = 280 | issue = 16 | pages = 16368–76 | date = April 2005 | pmid = 15713661 | doi = 10.1074/jbc.M500912200 | url = http://www.jbc.org/content/280/16/16368.long }}</ref> The gamma phosphate at the 5' end of 7SK is methylated by the methylphosphate capping enzyme MEPCE which is a constitutive component of the 7SK snRNP.<ref>{{cite journal | vauthors = Jeronimo C, Forget D, Bouchard A, Li Q, Chua G, Poitras C, Thérien C, Bergeron D, Bourassa S, Greenblatt J, Chabot B, Poirier GG, Hughes TR, Blanchette M, Price DH, Coulombe B | title = Systematic analysis of the protein interaction network for the human transcription machinery reveals the identity of the 7SK capping enzyme | journal = Molecular Cell | volume = 27 | issue = 2 | pages = 262–74 | date = July 2007 | pmid = 17643375 | doi = 10.1016/j.molcel.2007.06.027 | url = http://www.sciencedirect.com/science/article/pii/S1097276507004170 }}</ref>  A La related protein LARP7 is also found associated with 7SK, presumably in part through its interaction with the 3' end of the RNA.<ref>{{cite journal | vauthors = Krueger BJ, Jeronimo C, Roy BB, Bouchard A, Barrandon C, Byers SA, Searcey CE, Cooper JJ, Bensaude O, Cohen EA, Coulombe B, Price DH | title = LARP7 is a stable component of the 7SK snRNP while P-TEFb, HEXIM1 and hnRNP A1 are reversibly associated | journal = Nucleic Acids Research | volume = 36 | issue = 7 | pages = 2219–29 | date = April 2008 | pmid = 18281698 | pmc = 2367717 | doi = 10.1093/nar/gkn061 | url = http://nar.oxfordjournals.org/content/36/7/2219.long }}</ref><ref>{{cite journal | vauthors = Markert A, Grimm M, Martinez J, Wiesner J, Meyerhans A, Meyuhas O, Sickmann A, Fischer U | title = The La-related protein LARP7 is a component of the 7SK ribonucleoprotein and affects transcription of cellular and viral polymerase II genes | journal = EMBO Reports | volume = 9 | issue = 6 | pages = 569–75 | date = June 2008 | pmid = 18483487 | pmc = 2427381 | doi = 10.1038/embor.2008.72 | url = http://www.nature.com/embor/journal/v9/n6/full/embor200872.html }}</ref><ref>{{cite journal | vauthors = He N, Jahchan NS, Hong E, Li Q, Bayfield MA, Maraia RJ, Luo K, Zhou Q | title = A La-related protein modulates 7SK snRNP integrity to suppress P-TEFb-dependent transcriptional elongation and tumorigenesis | journal = Molecular Cell | volume = 29 | issue = 5 | pages = 588–99 | date = March 2008 | pmid = 18249148 | doi = 10.1016/j.molcel.2008.01.003 | url = http://www.sciencedirect.com/science/article/pii/S1097276508000361 }}</ref>    Reduction of either MEPCE or LARP7 by siRNA mediated knockdown leads to destabilization of 7SK in vivo.  A subset of 7SK snRNPs lack P-TEFb and HEXIM, but contains hnRNPs instead.<ref>url = https://academic.oup.com/nar/article/44/16/7527/2460216/Cracking-the-control-of-RNA-polymerase-II</ref>
An early study indicated that 7SK in cells is associated with a number of proteins and [[RNA structure probing|probing]] of the [[RNA structure|secondary structure]] suggested a model for [[base pair]]ing between different regions of the RNA.<ref>{{cite journal | vauthors = Wassarman DA, Steitz JA | title = Structural analyses of the 7SK ribonucleoprotein (RNP), the most abundant human small RNP of unknown function | journal = Molecular and Cellular Biology | volume = 11 | issue = 7 | pages = 3432–45 | date = July 1991 | pmid = 1646389 | pmc = 361072 | doi = 10.1128/MCB.11.7.3432 | url = http://mcb.asm.org/content/11/7/3432.long }}</ref> A breakthrough in the function of the 7SK snRNP came with the finding that the positive transcription elongation factor P-TEFb was a component of the complex.<ref>{{cite journal | vauthors = Nguyen VT, Kiss T, Michels AA, Bensaude O | title = 7SK small nuclear RNA binds to and inhibits the activity of CDK9/cyclin T complexes | journal = Nature | volume = 414 | issue = 6861 | pages = 322–5 | date = November 2001 | pmid = 11713533 | doi = 10.1038/35104581 | url = http://www.nature.com/nature/journal/v414/n6861/full/414322a0.html }}</ref><ref>{{cite journal | vauthors = Yang Z, Zhu Q, Luo K, Zhou Q | title = The 7SK small nuclear RNA inhibits the CDK9/cyclin T1 kinase to control transcription | journal = Nature | volume = 414 | issue = 6861 | pages = 317–22 | date = November 2001 | pmid = 11713532 | doi = 10.1038/35104575 | url = http://www.nature.com/nature/journal/v414/n6861/full/414317a0.html }}</ref> 7SK associates with and inhibits the cyclin dependent kinase activity of P-TEFb through the action of the RNA binding proteins [[HEXIM1]]<ref>{{cite journal | vauthors = Michels AA, Nguyen VT, Fraldi A, Labas V, Edwards M, Bonnet F, Lania L, Bensaude O | title = MAQ1 and 7SK RNA interact with CDK9/cyclin T complexes in a transcription-dependent manner | journal = Molecular and Cellular Biology | volume = 23 | issue = 14 | pages = 4859–69 | date = July 2003 | pmid = 12832472 | pmc = 162212 | doi = 10.1128/MCB.23.14.4859-4869.2003 | url = http://mcb.asm.org/content/23/14/4859.long }}</ref><ref>{{cite journal | vauthors = Yik JH, Chen R, Nishimura R, Jennings JL, Link AJ, Zhou Q | title = Inhibition of P-TEFb (CDK9/Cyclin T) kinase and RNA polymerase II transcription by the coordinated actions of HEXIM1 and 7SK snRNA | journal = Molecular Cell | volume = 12 | issue = 4 | pages = 971–82 | date = October 2003 | pmid = 14580347 | doi = 10.1016/S1097-2765(03)00388-5 | url = http://www.sciencedirect.com/science/article/pii/S1097276503003885 }}</ref> or [[HEXIM2]].<ref>{{cite journal | vauthors = Byers SA, Price JP, Cooper JJ, Li Q, Price DH | title = HEXIM2, a HEXIM1-related protein, regulates positive transcription elongation factor b through association with 7SK | journal = The Journal of Biological Chemistry | volume = 280 | issue = 16 | pages = 16360–7 | date = April 2005 | pmid = 15713662 | doi = 10.1074/jbc.M500424200 | url = http://www.jbc.org/content/280/16/16360.long }}</ref><ref>{{cite journal | vauthors = Yik JH, Chen R, Pezda AC, Zhou Q | title = Compensatory contributions of HEXIM1 and HEXIM2 in maintaining the balance of active and inactive positive transcription elongation factor b complexes for control of transcription | journal = The Journal of Biological Chemistry | volume = 280 | issue = 16 | pages = 16368–76 | date = April 2005 | pmid = 15713661 | doi = 10.1074/jbc.M500912200 | url = http://www.jbc.org/content/280/16/16368.long }}</ref> The gamma phosphate at the 5' end of 7SK is methylated by the methylphosphate capping enzyme MEPCE which is a constitutive component of the 7SK snRNP.<ref>{{cite journal | vauthors = Jeronimo C, Forget D, Bouchard A, Li Q, Chua G, Poitras C, Thérien C, Bergeron D, Bourassa S, Greenblatt J, Chabot B, Poirier GG, Hughes TR, Blanchette M, Price DH, Coulombe B | title = Systematic analysis of the protein interaction network for the human transcription machinery reveals the identity of the 7SK capping enzyme | journal = Molecular Cell | volume = 27 | issue = 2 | pages = 262–74 | date = July 2007 | pmid = 17643375 | doi = 10.1016/j.molcel.2007.06.027 | url = http://www.sciencedirect.com/science/article/pii/S1097276507004170 | pmc=4498903}}</ref>  A La related protein LARP7 is also found associated with 7SK, presumably in part through its interaction with the 3' end of the RNA.<ref>{{cite journal | vauthors = Krueger BJ, Jeronimo C, Roy BB, Bouchard A, Barrandon C, Byers SA, Searcey CE, Cooper JJ, Bensaude O, Cohen EA, Coulombe B, Price DH | title = LARP7 is a stable component of the 7SK snRNP while P-TEFb, HEXIM1 and hnRNP A1 are reversibly associated | journal = Nucleic Acids Research | volume = 36 | issue = 7 | pages = 2219–29 | date = April 2008 | pmid = 18281698 | pmc = 2367717 | doi = 10.1093/nar/gkn061 | url = http://nar.oxfordjournals.org/content/36/7/2219.long }}</ref><ref>{{cite journal | vauthors = Markert A, Grimm M, Martinez J, Wiesner J, Meyerhans A, Meyuhas O, Sickmann A, Fischer U | title = The La-related protein LARP7 is a component of the 7SK ribonucleoprotein and affects transcription of cellular and viral polymerase II genes | journal = EMBO Reports | volume = 9 | issue = 6 | pages = 569–75 | date = June 2008 | pmid = 18483487 | pmc = 2427381 | doi = 10.1038/embor.2008.72 | url = http://www.nature.com/embor/journal/v9/n6/full/embor200872.html }}</ref><ref>{{cite journal | vauthors = He N, Jahchan NS, Hong E, Li Q, Bayfield MA, Maraia RJ, Luo K, Zhou Q | title = A La-related protein modulates 7SK snRNP integrity to suppress P-TEFb-dependent transcriptional elongation and tumorigenesis | journal = Molecular Cell | volume = 29 | issue = 5 | pages = 588–99 | date = March 2008 | pmid = 18249148 | doi = 10.1016/j.molcel.2008.01.003 | url = http://www.sciencedirect.com/science/article/pii/S1097276508000361 }}</ref>    Reduction of either MEPCE or LARP7 by siRNA mediated knockdown leads to destabilization of 7SK in vivo.  A subset of 7SK snRNPs lack P-TEFb and HEXIM, but contains hnRNPs instead.<ref>url = https://academic.oup.com/nar/article/44/16/7527/2460216/Cracking-the-control-of-RNA-polymerase-II</ref>


== Function ==
== Function ==
The major function of the 7SK snRNP is control of the P-TEFb, a factor that regulates the elongation phase of transcription.<ref name="Peterlin"/>  The kinase activity of P-TEFb is inhibited when the factor is in the 7SK snRNP.  P-TEFb can be released from the 7SK snRNP by either the HIV transactivator [[Tat (HIV)|Tat]] or the [[bromodomain]] containing protein [[BRD4]].  This release leads to a conformational change in 7SK RNA and the ejection of HEXIM.<ref>{{cite journal | vauthors = Krueger BJ, Varzavand K, Cooper JJ, Price DH | title = The mechanism of release of P-TEFb and HEXIM1 from the 7SK snRNP by viral and cellular activators includes a conformational change in 7SK | journal = PLoS One | volume = 5 | issue = 8 | pages = e12335 | date = August 2010 | pmid = 20808803 | pmc = 2925947 | doi = 10.1371/journal.pone.0012335 | url = http://www.plosone.org/article/info%3Adoi%2F10.1371%2Fjournal.pone.0012335 | editor1-last = Blagosklonny | editor1-first = Mikhail V. }}</ref>  hnRNPs stabilize the complex lacking P-TEFb and HEXIM.  After P-TEFb functions on specific genes it is re-sequestered in the 7SK snRNP by an unknown mechanism.  The 7SK snRNP has been characterized in both human and Drosophila.<ref>{{cite journal | vauthors = Nguyen D, Krueger BJ, Sedore SC, Brogie JE, Rogers JT, Rajendra TK, Saunders A, Matera AG, Lis JT, Uguen P, Price DH | title = The Drosophila 7SK snRNP and the essential role of dHEXIM in development | journal = Nucleic Acids Research | volume = 40 | issue = 12 | pages = 5283–97 | date = July 2012 | pmid = 22379134 | pmc = 3384314 | doi = 10.1093/nar/gks191 | url = http://nar.oxfordjournals.org/content/early/2012/02/29/nar.gks191.long }}</ref>  
The major function of the 7SK snRNP is control of the P-TEFb, a factor that regulates the elongation phase of transcription.<ref name="Peterlin"/>  The kinase activity of P-TEFb is inhibited when the factor is in the 7SK snRNP.  P-TEFb can be released from the 7SK snRNP by either the HIV transactivator [[Tat (HIV)|Tat]] or the [[bromodomain]] containing protein [[BRD4]].  This release leads to a conformational change in 7SK RNA and the ejection of HEXIM.<ref>{{cite journal | vauthors = Krueger BJ, Varzavand K, Cooper JJ, Price DH | title = The mechanism of release of P-TEFb and HEXIM1 from the 7SK snRNP by viral and cellular activators includes a conformational change in 7SK | journal = PLOS ONE | volume = 5 | issue = 8 | pages = e12335 | date = August 2010 | pmid = 20808803 | pmc = 2925947 | doi = 10.1371/journal.pone.0012335 | url = http://www.plosone.org/article/info%3Adoi%2F10.1371%2Fjournal.pone.0012335 | editor1-last = Blagosklonny | editor1-first = Mikhail V. }}</ref>  hnRNPs stabilize the complex lacking P-TEFb and HEXIM.  After P-TEFb functions on specific genes it is re-sequestered in the 7SK snRNP by an unknown mechanism.  The 7SK snRNP has been characterized in both human and Drosophila.<ref>{{cite journal | vauthors = Nguyen D, Krueger BJ, Sedore SC, Brogie JE, Rogers JT, Rajendra TK, Saunders A, Matera AG, Lis JT, Uguen P, Price DH | title = The Drosophila 7SK snRNP and the essential role of dHEXIM in development | journal = Nucleic Acids Research | volume = 40 | issue = 12 | pages = 5283–97 | date = July 2012 | pmid = 22379134 | pmc = 3384314 | doi = 10.1093/nar/gks191 | url = http://nar.oxfordjournals.org/content/early/2012/02/29/nar.gks191.long }}</ref>  
Detailed review.<ref>{{cite journal | vauthors = C Quaresma AJ, Bugai A, Barboric M | title = Cracking the control of RNA polymerase II elongation by 7SK snRNP and P-TEFb | journal = Nucleic Acids Research | volume = 44 | issue = 16 | pages = 7527–39 | date = September 2016 | pmid = 27369380 | pmc = 5027500 | doi = 10.1093/nar/gkw585 | url = http://nar.oxfordjournals.org/content/44/16/7527.long }}</ref>
Detailed review.<ref>{{cite journal | vauthors = C Quaresma AJ, Bugai A, Barboric M | title = Cracking the control of RNA polymerase II elongation by 7SK snRNP and P-TEFb | journal = Nucleic Acids Research | volume = 44 | issue = 16 | pages = 7527–39 | date = September 2016 | pmid = 27369380 | pmc = 5027500 | doi = 10.1093/nar/gkw585 | url = http://nar.oxfordjournals.org/content/44/16/7527.long }}</ref>


Latest revision as of 17:55, 12 November 2018

File:Regulation of P-TEFb by the 7SK snRNP.jpg
Reversible association of P-TEFb with the 7SK snRNP. P-TEFb is released from the 7SK snRNP by Brd4 or HIV Tat. HEXIM is ejected and the two proteins are replaced by hrRNPs. The reverse of this process requires other unknown factors.
7SK RNA
File:RF00100.jpg
Identifiers
Symbol7SK
RfamRF00100
Other data
RNA typeGene
Domain(s)Eukaryota
SO0000274
PDB structuresPDBe
RN7SK
Identifiers
SymbolRN7SK
Entrez125050
Other data
LocusChr. 6 p12.2

In molecular biology 7SK is an abundant small nuclear RNA found in metazoans.[1] It plays a role in regulating transcription by controlling the positive transcription elongation factor P-TEFb.[2] 7SK is found in a small nuclear ribonucleoprotein complex (snRNP) with a number of other proteins that regulate the stability and function of the complex.

Structure

An early study indicated that 7SK in cells is associated with a number of proteins and probing of the secondary structure suggested a model for base pairing between different regions of the RNA.[3] A breakthrough in the function of the 7SK snRNP came with the finding that the positive transcription elongation factor P-TEFb was a component of the complex.[4][5] 7SK associates with and inhibits the cyclin dependent kinase activity of P-TEFb through the action of the RNA binding proteins HEXIM1[6][7] or HEXIM2.[8][9] The gamma phosphate at the 5' end of 7SK is methylated by the methylphosphate capping enzyme MEPCE which is a constitutive component of the 7SK snRNP.[10] A La related protein LARP7 is also found associated with 7SK, presumably in part through its interaction with the 3' end of the RNA.[11][12][13] Reduction of either MEPCE or LARP7 by siRNA mediated knockdown leads to destabilization of 7SK in vivo. A subset of 7SK snRNPs lack P-TEFb and HEXIM, but contains hnRNPs instead.[14]

Function

The major function of the 7SK snRNP is control of the P-TEFb, a factor that regulates the elongation phase of transcription.[2] The kinase activity of P-TEFb is inhibited when the factor is in the 7SK snRNP. P-TEFb can be released from the 7SK snRNP by either the HIV transactivator Tat or the bromodomain containing protein BRD4. This release leads to a conformational change in 7SK RNA and the ejection of HEXIM.[15] hnRNPs stabilize the complex lacking P-TEFb and HEXIM. After P-TEFb functions on specific genes it is re-sequestered in the 7SK snRNP by an unknown mechanism. The 7SK snRNP has been characterized in both human and Drosophila.[16] Detailed review.[17]

References

  1. ↑ Diribarne G, Bensaude O (2009). "7SK RNA, a non-coding RNA regulating P-TEFb, a general transcription factor". RNA Biology. 6 (2): 122–8. doi:10.4161/rna.6.2.8115. PMID 19246988.
  2. ↑ 2.0 2.1 Peterlin BM, Brogie JE, Price DH (2012). "7SK snRNA: a noncoding RNA that plays a major role in regulating eukaryotic transcription". Wiley Interdisciplinary Reviews: RNA. 3 (1): 92–103. doi:10.1002/wrna.106. PMC 3223291. PMID 21853533.
  3. ↑ Wassarman DA, Steitz JA (July 1991). "Structural analyses of the 7SK ribonucleoprotein (RNP), the most abundant human small RNP of unknown function". Molecular and Cellular Biology. 11 (7): 3432–45. doi:10.1128/MCB.11.7.3432. PMC 361072. PMID 1646389.
  4. ↑ Nguyen VT, Kiss T, Michels AA, Bensaude O (November 2001). "7SK small nuclear RNA binds to and inhibits the activity of CDK9/cyclin T complexes". Nature. 414 (6861): 322–5. doi:10.1038/35104581. PMID 11713533.
  5. ↑ Yang Z, Zhu Q, Luo K, Zhou Q (November 2001). "The 7SK small nuclear RNA inhibits the CDK9/cyclin T1 kinase to control transcription". Nature. 414 (6861): 317–22. doi:10.1038/35104575. PMID 11713532.
  6. ↑ Michels AA, Nguyen VT, Fraldi A, Labas V, Edwards M, Bonnet F, Lania L, Bensaude O (July 2003). "MAQ1 and 7SK RNA interact with CDK9/cyclin T complexes in a transcription-dependent manner". Molecular and Cellular Biology. 23 (14): 4859–69. doi:10.1128/MCB.23.14.4859-4869.2003. PMC 162212. PMID 12832472.
  7. ↑ Yik JH, Chen R, Nishimura R, Jennings JL, Link AJ, Zhou Q (October 2003). "Inhibition of P-TEFb (CDK9/Cyclin T) kinase and RNA polymerase II transcription by the coordinated actions of HEXIM1 and 7SK snRNA". Molecular Cell. 12 (4): 971–82. doi:10.1016/S1097-2765(03)00388-5. PMID 14580347.
  8. ↑ Byers SA, Price JP, Cooper JJ, Li Q, Price DH (April 2005). "HEXIM2, a HEXIM1-related protein, regulates positive transcription elongation factor b through association with 7SK". The Journal of Biological Chemistry. 280 (16): 16360–7. doi:10.1074/jbc.M500424200. PMID 15713662.
  9. ↑ Yik JH, Chen R, Pezda AC, Zhou Q (April 2005). "Compensatory contributions of HEXIM1 and HEXIM2 in maintaining the balance of active and inactive positive transcription elongation factor b complexes for control of transcription". The Journal of Biological Chemistry. 280 (16): 16368–76. doi:10.1074/jbc.M500912200. PMID 15713661.
  10. ↑ Jeronimo C, Forget D, Bouchard A, Li Q, Chua G, Poitras C, Thérien C, Bergeron D, Bourassa S, Greenblatt J, Chabot B, Poirier GG, Hughes TR, Blanchette M, Price DH, Coulombe B (July 2007). "Systematic analysis of the protein interaction network for the human transcription machinery reveals the identity of the 7SK capping enzyme". Molecular Cell. 27 (2): 262–74. doi:10.1016/j.molcel.2007.06.027. PMC 4498903. PMID 17643375.
  11. ↑ Krueger BJ, Jeronimo C, Roy BB, Bouchard A, Barrandon C, Byers SA, Searcey CE, Cooper JJ, Bensaude O, Cohen EA, Coulombe B, Price DH (April 2008). "LARP7 is a stable component of the 7SK snRNP while P-TEFb, HEXIM1 and hnRNP A1 are reversibly associated". Nucleic Acids Research. 36 (7): 2219–29. doi:10.1093/nar/gkn061. PMC 2367717. PMID 18281698.
  12. ↑ Markert A, Grimm M, Martinez J, Wiesner J, Meyerhans A, Meyuhas O, Sickmann A, Fischer U (June 2008). "The La-related protein LARP7 is a component of the 7SK ribonucleoprotein and affects transcription of cellular and viral polymerase II genes". EMBO Reports. 9 (6): 569–75. doi:10.1038/embor.2008.72. PMC 2427381. PMID 18483487.
  13. ↑ He N, Jahchan NS, Hong E, Li Q, Bayfield MA, Maraia RJ, Luo K, Zhou Q (March 2008). "A La-related protein modulates 7SK snRNP integrity to suppress P-TEFb-dependent transcriptional elongation and tumorigenesis". Molecular Cell. 29 (5): 588–99. doi:10.1016/j.molcel.2008.01.003. PMID 18249148.
  14. ↑ url = https://academic.oup.com/nar/article/44/16/7527/2460216/Cracking-the-control-of-RNA-polymerase-II
  15. ↑ Krueger BJ, Varzavand K, Cooper JJ, Price DH (August 2010). Blagosklonny MV, ed. "The mechanism of release of P-TEFb and HEXIM1 from the 7SK snRNP by viral and cellular activators includes a conformational change in 7SK". PLOS ONE. 5 (8): e12335. doi:10.1371/journal.pone.0012335. PMC 2925947. PMID 20808803.
  16. ↑ Nguyen D, Krueger BJ, Sedore SC, Brogie JE, Rogers JT, Rajendra TK, Saunders A, Matera AG, Lis JT, Uguen P, Price DH (July 2012). "The Drosophila 7SK snRNP and the essential role of dHEXIM in development". Nucleic Acids Research. 40 (12): 5283–97. doi:10.1093/nar/gks191. PMC 3384314. PMID 22379134.
  17. ↑ C Quaresma AJ, Bugai A, Barboric M (September 2016). "Cracking the control of RNA polymerase II elongation by 7SK snRNP and P-TEFb". Nucleic Acids Research. 44 (16): 7527–39. doi:10.1093/nar/gkw585. PMC 5027500. PMID 27369380.

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