Literature DB >> 15128671

Quantitative contributions of CtBP-dependent and -independent repression activities of Knirps.

Paolo Struffi1, Maria Corado, Meghana Kulkarni, David N Arnosti.   

Abstract

The Drosophila Knirps protein is a short-range transcriptional repressor that locally inhibits activators by recruiting the CtBP co-repressor. Knirps also possesses CtBP-independent repression activity. The functional importance of multiple repression activities is not well understood, but the finding that Knirps does not repress some cis-regulatory elements in the absence of CtBP suggested that the co-factor may supply a unique function essential to repress certain types of activators. We assayed CtBP-dependent and -independent repression domains of Knirps in Drosophila embryos, and found that the CtBP-independent activity, when provided at higher than normal levels, can repress an eve regulatory element that normally requires CtBP. Dose response analysis revealed that the activity of Knirps containing both CtBP-dependent and -independent repression activities is higher than that of the CtBP-independent domain alone. The requirement for CtBP at certain enhancers appears to reflect the need for overall higher levels of repression, rather than a requirement for an activity unique to CtBP. Thus, CtBP contributes quantitatively, rather than qualitatively, to overall repression function. The finding that both repression activities are simultaneously deployed suggests that the multiple repression activities do not function as cryptic 'backup' systems, but that each contributes quantitatively to total repressor output.

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Year:  2004        PMID: 15128671     DOI: 10.1242/dev.01075

Source DB:  PubMed          Journal:  Development        ISSN: 0950-1991            Impact factor:   6.868


  14 in total

1.  CtBP contributes quantitatively to Knirps repression activity in an NAD binding-dependent manner.

Authors:  Montserrat Sutrias-Grau; David N Arnosti
Journal:  Mol Cell Biol       Date:  2004-07       Impact factor: 4.272

2.  Quantitatively predictable control of Drosophila transcriptional enhancers in vivo with engineered transcription factors.

Authors:  Justin Crocker; Garth R Ilsley; David L Stern
Journal:  Nat Genet       Date:  2016-02-08       Impact factor: 38.330

3.  cis-regulatory logic of short-range transcriptional repression in Drosophila melanogaster.

Authors:  Meghana M Kulkarni; David N Arnosti
Journal:  Mol Cell Biol       Date:  2005-05       Impact factor: 4.272

4.  Groucho corepressor functions as a cofactor for the Knirps short-range transcriptional repressor.

Authors:  Sandhya Payankaulam; David N Arnosti
Journal:  Proc Natl Acad Sci U S A       Date:  2009-09-28       Impact factor: 11.205

5.  Functional interaction between the Drosophila knirps short range transcriptional repressor and RPD3 histone deacetylase.

Authors:  Paolo Struffi; David N Arnosti
Journal:  J Biol Chem       Date:  2005-09-26       Impact factor: 5.157

6.  Combinatorial activation and concentration-dependent repression of the Drosophila even skipped stripe 3+7 enhancer.

Authors:  Paolo Struffi; Maria Corado; Leah Kaplan; Danyang Yu; Christine Rushlow; Stephen Small
Journal:  Development       Date:  2011-08-24       Impact factor: 6.868

7.  Long- and short-range transcriptional repressors induce distinct chromatin states on repressed genes.

Authors:  Li M Li; David N Arnosti
Journal:  Curr Biol       Date:  2011-02-25       Impact factor: 10.834

8.  The oligomeric state of CtBP determines its role as a transcriptional co-activator and co-repressor of Wingless targets.

Authors:  Chandan Bhambhani; Jinhee L Chang; David L Akey; Ken M Cadigan
Journal:  EMBO J       Date:  2011-04-05       Impact factor: 11.598

9.  Drosophila Ebi mediates Snail-dependent transcriptional repression through HDAC3-induced histone deacetylation.

Authors:  Dai Qi; Mattias Bergman; Hitoshi Aihara; Yutaka Nibu; Mattias Mannervik
Journal:  EMBO J       Date:  2008-02-28       Impact factor: 11.598

10.  Brinker possesses multiple mechanisms for repression because its primary co-repressor, Groucho, may be unavailable in some cell types.

Authors:  Priyanka Upadhyai; Gerard Campbell
Journal:  Development       Date:  2013-10       Impact factor: 6.868

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