Literature DB >> 8601337

Phosphorylation dependence of the initiation of productive transcription of Balbiani ring 2 genes in living cells.

E Egyházi1, A Ossoinak, A Pigon, C Holmgren, J M Lee, A L Greenleaf.   

Abstract

Using polytene chromosomes of salivary gland cells of Chironomus tentans, phosphorylation state-sensitive antibodies and the transcription and protein kinase inhibitor 5,6-dichloro-1-beta-D-ribofuranosylbenzimidazole (DRB), we have visualized the chromosomal distribution of RNA polymerase II (pol II) with hypophosphorylated (pol IIA) and hyperphosphorylated (pol II0) carboxyl-terminal repeat domain (CTD). DRB blocks labeling of the CTD with 32Pi within minutes of its addition, and nuclear pol II0 is gradually converted to IIA; this conversion parallels the reduction in transcription of protein-coding genes. DRB also alters the chromosomal distribution of II0: there is a time-dependent clearance from chromosomes of phosphoCTD (PCTD) after addition of DRB, which coincides in time with the completion and release of preinitiated transcripts. Furthermore, the staining of smaller transcription units is abolished before that of larger ones. The staining pattern of chromosomes with anti-CTD antibodies is not detectably influenced by the DRB treatment, indicating that hypophosphorylated pol IIA is unaffected by the transcription inhibitor. Microinjection of synthetic heptapeptide repeats, anti-CTD and anti-PCTD antibodies into salivary gland nuclei hampered the transcription of BR2 genes, indicating the requirement for CTD and PCTD in transcription in living cells. The results demonstrate that in vivo the protein kinase effector DRB shows parallel effects on an early step in gene transcription and the process of pol II hyperphosphorylation. Our observations are consistent with the proposal that the initiation of productive RNA synthesis is CTD-phosphorylation dependent and also with the idea that the gradual dephosphorylation of transcribing pol II0 is coupled to the completion of nascent pol II gene transcripts.

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Year:  1996        PMID: 8601337     DOI: 10.1007/bf00352266

Source DB:  PubMed          Journal:  Chromosoma        ISSN: 0009-5915            Impact factor:   4.316


  71 in total

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Authors:  C PELLING
Journal:  Chromosoma       Date:  1964-04-01       Impact factor: 4.316

2.  Specific interaction between the nonphosphorylated form of RNA polymerase II and the TATA-binding protein.

Authors:  A Usheva; E Maldonado; A Goldring; H Lu; C Houbavi; D Reinberg; Y Aloni
Journal:  Cell       Date:  1992-05-29       Impact factor: 41.582

3.  Quantitation of turnover and export to the cytoplasm of hnRNA transcribed in the Balbiani rings.

Authors:  E Egyházi
Journal:  Cell       Date:  1976-04       Impact factor: 41.582

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Authors:  E Egyhazi
Journal:  Nature       Date:  1976-07-22       Impact factor: 49.962

5.  Purification and characterization of a template-associated protein kinase that phosphorylates RNA polymerase II.

Authors:  A Dvir; L Y Stein; B L Calore; W S Dynan
Journal:  J Biol Chem       Date:  1993-05-15       Impact factor: 5.157

6.  Early termination of heterogeneous nuclear RNA transcripts in mammalian cells: accentuation by 5,6-dichloro 1-beta-D-ribofuranosylbenzimidazole.

Authors:  I Tamm; T Kikuchi
Journal:  Proc Natl Acad Sci U S A       Date:  1979-11       Impact factor: 11.205

7.  Functional redundancy and structural polymorphism in the large subunit of RNA polymerase II.

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Journal:  Cell       Date:  1987-09-11       Impact factor: 41.582

8.  5,6-Dichloro-1-beta-D-ribofuranosylbenzimidazole inhibits transcription of the beta-hemoglobin gene in vivo at initiation.

Authors:  R Mukherjee; G R Molloy
Journal:  J Biol Chem       Date:  1987-10-05       Impact factor: 5.157

9.  Human general transcription factor IIH phosphorylates the C-terminal domain of RNA polymerase II.

Authors:  H Lu; L Zawel; L Fisher; J M Egly; D Reinberg
Journal:  Nature       Date:  1992-08-20       Impact factor: 49.962

10.  Relationship of CDK-activating kinase and RNA polymerase II CTD kinase TFIIH/TFIIK.

Authors:  W J Feaver; J Q Svejstrup; N L Henry; R D Kornberg
Journal:  Cell       Date:  1994-12-16       Impact factor: 41.582

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  13 in total

Review 1.  P-TEFb, a cyclin-dependent kinase controlling elongation by RNA polymerase II.

Authors:  D H Price
Journal:  Mol Cell Biol       Date:  2000-04       Impact factor: 4.272

Review 2.  RNA polymerase II elongation control.

Authors:  Qiang Zhou; Tiandao Li; David H Price
Journal:  Annu Rev Biochem       Date:  2012-03-09       Impact factor: 23.643

3.  RNA polymerase II carboxy-terminal domain phosphorylation is required for cotranscriptional pre-mRNA splicing and 3'-end formation.

Authors:  Gregory Bird; Diego A R Zorio; David L Bentley
Journal:  Mol Cell Biol       Date:  2004-10       Impact factor: 4.272

4.  Brd4 coactivates transcriptional activation of NF-kappaB via specific binding to acetylated RelA.

Authors:  Bo Huang; Xiao-Dong Yang; Ming-Ming Zhou; Keiko Ozato; Lin-Feng Chen
Journal:  Mol Cell Biol       Date:  2008-12-22       Impact factor: 4.272

Review 5.  RNA polymerase II transcription elongation control.

Authors:  Jiannan Guo; David H Price
Journal:  Chem Rev       Date:  2013-08-06       Impact factor: 60.622

6.  Transcription elongation factor P-TEFb is required for HIV-1 tat transactivation in vitro.

Authors:  Y Zhu; T Pe'ery; J Peng; Y Ramanathan; N Marshall; T Marshall; B Amendt; M B Mathews; D H Price
Journal:  Genes Dev       Date:  1997-10-15       Impact factor: 11.361

7.  Heat-shock inactivation of the TFIIH-associated kinase and change in the phosphorylation sites on the C-terminal domain of RNA polymerase II.

Authors:  M F Dubois; M Vincent; M Vigneron; J Adamczewski; J M Egly; O Bensaude
Journal:  Nucleic Acids Res       Date:  1997-02-15       Impact factor: 16.971

8.  The binding of the alpha subunit of protein kinase CK2 and RAP74 subunit of TFIIF to protein-coding genes in living cells is DRB sensitive.

Authors:  E Egyházi; A Ossoinak; O Filhol-Cochet; C Cochet; A Pigon
Journal:  Mol Cell Biochem       Date:  1999-01       Impact factor: 3.396

9.  The trithorax group proteins Kismet and ASH1 promote H3K36 dimethylation to counteract Polycomb group repression in Drosophila.

Authors:  Kristel M Dorighi; John W Tamkun
Journal:  Development       Date:  2013-09-04       Impact factor: 6.868

10.  P-TEFb is critical for the maturation of RNA polymerase II into productive elongation in vivo.

Authors:  Zhuoyu Ni; Abbie Saunders; Nicholas J Fuda; Jie Yao; Jose-Ramon Suarez; Watt W Webb; John T Lis
Journal:  Mol Cell Biol       Date:  2007-12-10       Impact factor: 4.272

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