» Articles » PMID: 2693207

Intragenic and Extragenic Suppressors of Mutations in the Heptapeptide Repeat Domain of Saccharomyces Cerevisiae RNA Polymerase II

Overview
Journal Genetics
Specialty Genetics
Date 1989 Dec 1
PMID 2693207
Citations 115
Authors
Affiliations
Soon will be listed here.
Abstract

The largest subunit of RNA polymerase II contains a repeated heptapeptide sequence at its carboxy terminus. Yeast mutants with certain partial deletions of the carboxy-terminal repeat (CTR) domain are temperature-sensitive, cold-sensitive and are inositol auxotrophs. Intragenic and extragenic suppressors of the cold-sensitive phenotype of CTR domain deletion mutants were isolated and studied to investigate the function of this domain. Two types of intragenic suppressing mutations suppress the temperature-sensitivity, cold-sensitivity and inositol auxotrophy of CTR domain deletion mutants. Most intragenic mutations enlarge the repeat domain by duplicating various portions of the repeat coding sequence. Other intragenic suppressing mutations are point mutations in a conserved segment of the large subunit. An extragenic suppressing mutation (SRB2-1) was isolated that strongly suppresses the conditional and auxotrophic phenotypes of CTR domain mutations. The SRB2 gene was isolated and mapped, and an SRB2 partial deletion mutation (srb2 delta 10) was constructed. The srb2 delta 10 mutants are temperature-sensitive, cold-sensitive and are inositol auxotrophs. These phenotypes are characteristic of mutations in genes encoding components of the transcription apparatus. We propose that the SRB2 gene encodes a factor that is involved in RNA synthesis and may interact with the CTR domain of the large subunit of RNA polymerase II.

Citing Articles

Yeast PIC-Mediator structure with RNA polymerase II C-terminal domain.

Schilbach S, Wang H, Dienemann C, Cramer P Proc Natl Acad Sci U S A. 2023; 120(15):e2220542120.

PMID: 37014863 PMC: 10104585. DOI: 10.1073/pnas.2220542120.


Function and dynamics of the Mediator complex: novel insights and new frontiers.

Morse R Transcription. 2022; 13(1-3):39-52.

PMID: 35708525 PMC: 9467533. DOI: 10.1080/21541264.2022.2085502.


Suppressor Mutants: History and Today's Applications.

Bautista D, Carr J, Mitchell A EcoSal Plus. 2021; 9(2):eESP00372020.

PMID: 34910591 PMC: 9008745. DOI: 10.1128/ecosalplus.ESP-0037-2020.


Transcription activation depends on the length of the RNA polymerase II C-terminal domain.

Sawicka A, Villamil G, Lidschreiber M, Darzacq X, Dugast-Darzacq C, Schwalb B EMBO J. 2021; 40(9):e107015.

PMID: 33555055 PMC: 8090853. DOI: 10.15252/embj.2020107015.


Functional interplay between Mediator and RNA polymerase II in Rad2/XPG loading to the chromatin.

Georges A, Gopaul D, Denby Wilkes C, Giordanengo Aiach N, Novikova E, Barrault M Nucleic Acids Res. 2019; 47(17):8988-9004.

PMID: 31299084 PMC: 6753472. DOI: 10.1093/nar/gkz598.


References
1.
Woychik N, Young R . RNA polymerase II subunit RPB4 is essential for high- and low-temperature yeast cell growth. Mol Cell Biol. 1989; 9(7):2854-9. PMC: 362751. DOI: 10.1128/mcb.9.7.2854-2859.1989. View

2.
Kim W, Dahmus M . The major late promoter of adenovirus-2 is accurately transcribed by RNA polymerases IIO, IIA, and IIB. J Biol Chem. 1989; 264(6):3169-76. View

3.
Culbertson M, Henry S . Inositol-requiring mutants of Saccharomyces cerevisiae. Genetics. 1975; 80(1):23-40. PMC: 1213318. DOI: 10.1093/genetics/80.1.23. View

4.
Ovchinnikov YuA , Monastyrskaya G, Gubanov V, Guryev S, Salomatina I, Shuvaeva T . The primary structure of E. coli RNA polymerase, Nucleotide sequence of the rpoC gene and amino acid sequence of the beta'-subunit. Nucleic Acids Res. 1982; 10(13):4035-44. PMC: 320776. DOI: 10.1093/nar/10.13.4035. View

5.
Ito H, Fukuda Y, Murata K, Kimura A . Transformation of intact yeast cells treated with alkali cations. J Bacteriol. 1983; 153(1):163-8. PMC: 217353. DOI: 10.1128/jb.153.1.163-168.1983. View