The NC2 α and β subunits play different roles in vivo

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The NC2 α and β subunits play different roles in vivo. / Creton, Sandrine; Svejstrup, Jesper Q.; Collart, Martine A.

In: Genes and Development, Vol. 16, No. 24, 15.12.2002, p. 3265-3276.

Research output: Contribution to journalJournal articleResearchpeer-review

Harvard

Creton, S, Svejstrup, JQ & Collart, MA 2002, 'The NC2 α and β subunits play different roles in vivo', Genes and Development, vol. 16, no. 24, pp. 3265-3276. https://doi.org/10.1101/gad.234002

APA

Creton, S., Svejstrup, J. Q., & Collart, M. A. (2002). The NC2 α and β subunits play different roles in vivo. Genes and Development, 16(24), 3265-3276. https://doi.org/10.1101/gad.234002

Vancouver

Creton S, Svejstrup JQ, Collart MA. The NC2 α and β subunits play different roles in vivo. Genes and Development. 2002 Dec 15;16(24):3265-3276. https://doi.org/10.1101/gad.234002

Author

Creton, Sandrine ; Svejstrup, Jesper Q. ; Collart, Martine A. / The NC2 α and β subunits play different roles in vivo. In: Genes and Development. 2002 ; Vol. 16, No. 24. pp. 3265-3276.

Bibtex

@article{ac4ce4d8d7b747eeab16a5ac85b4e3b2,
title = "The NC2 α and β subunits play different roles in vivo",
abstract = "NC2 is a heterodimeric regulator of transcription that plays both positive and negative roles in vivo. Here we show that the α and β subunits of yeast NC2 are not always associated in a tight complex. Rather, their association is regulated, in particular by glucose depletion. Indeed, stable NC2 α/β complexes can only be purified from cells after the diauxic shift when glucose has been depleted from the growth medium. In vivo, the presence of NC2 α, but not NC2 β, at promoters generally correlates with the presence of TBP and transcriptional activity. In contrast, increased presence of NC2 β relative to TBP correlates with transcriptional repression. NC2 is regulated by phosphorylation. We found that mutation of genes encoding casein kinase II (CKII) subunits as well as potential CKII phosphorylation sites in NC2 α and β affected gene repression. Interestingly, NC2-dependent repression in the phosphorylation site mutants was only perturbed in high glucose when NC2 β and NC2 α are not associated, but not after the diauxic shift when NC2 α and β form stable complexes. Thus, the separation of NC2 α and β function indicated by these mutants also supports the existence of multiple NC2 complexes with different functions in transcription.",
keywords = "Casein kinase II, Diauxic shift, NC2, Transcriptional repression, Yeast",
author = "Sandrine Creton and Svejstrup, {Jesper Q.} and Collart, {Martine A.}",
year = "2002",
month = dec,
day = "15",
doi = "10.1101/gad.234002",
language = "English",
volume = "16",
pages = "3265--3276",
journal = "Genes & Development",
issn = "0890-9369",
publisher = "Cold Spring Harbor Laboratory Press",
number = "24",

}

RIS

TY - JOUR

T1 - The NC2 α and β subunits play different roles in vivo

AU - Creton, Sandrine

AU - Svejstrup, Jesper Q.

AU - Collart, Martine A.

PY - 2002/12/15

Y1 - 2002/12/15

N2 - NC2 is a heterodimeric regulator of transcription that plays both positive and negative roles in vivo. Here we show that the α and β subunits of yeast NC2 are not always associated in a tight complex. Rather, their association is regulated, in particular by glucose depletion. Indeed, stable NC2 α/β complexes can only be purified from cells after the diauxic shift when glucose has been depleted from the growth medium. In vivo, the presence of NC2 α, but not NC2 β, at promoters generally correlates with the presence of TBP and transcriptional activity. In contrast, increased presence of NC2 β relative to TBP correlates with transcriptional repression. NC2 is regulated by phosphorylation. We found that mutation of genes encoding casein kinase II (CKII) subunits as well as potential CKII phosphorylation sites in NC2 α and β affected gene repression. Interestingly, NC2-dependent repression in the phosphorylation site mutants was only perturbed in high glucose when NC2 β and NC2 α are not associated, but not after the diauxic shift when NC2 α and β form stable complexes. Thus, the separation of NC2 α and β function indicated by these mutants also supports the existence of multiple NC2 complexes with different functions in transcription.

AB - NC2 is a heterodimeric regulator of transcription that plays both positive and negative roles in vivo. Here we show that the α and β subunits of yeast NC2 are not always associated in a tight complex. Rather, their association is regulated, in particular by glucose depletion. Indeed, stable NC2 α/β complexes can only be purified from cells after the diauxic shift when glucose has been depleted from the growth medium. In vivo, the presence of NC2 α, but not NC2 β, at promoters generally correlates with the presence of TBP and transcriptional activity. In contrast, increased presence of NC2 β relative to TBP correlates with transcriptional repression. NC2 is regulated by phosphorylation. We found that mutation of genes encoding casein kinase II (CKII) subunits as well as potential CKII phosphorylation sites in NC2 α and β affected gene repression. Interestingly, NC2-dependent repression in the phosphorylation site mutants was only perturbed in high glucose when NC2 β and NC2 α are not associated, but not after the diauxic shift when NC2 α and β form stable complexes. Thus, the separation of NC2 α and β function indicated by these mutants also supports the existence of multiple NC2 complexes with different functions in transcription.

KW - Casein kinase II

KW - Diauxic shift

KW - NC2

KW - Transcriptional repression

KW - Yeast

U2 - 10.1101/gad.234002

DO - 10.1101/gad.234002

M3 - Journal article

C2 - 12502746

AN - SCOPUS:0037115591

VL - 16

SP - 3265

EP - 3276

JO - Genes & Development

JF - Genes & Development

SN - 0890-9369

IS - 24

ER -

ID: 331042187