Literature DB >> 23575308

Chromatin occupancy patterns of the ETS repressor Yan: a mechanism for buffering gene expression against noise?

Jemma L Webber1, Ilaria Rebay.   

Abstract

Developmental programs are driven by transcription factors that coordinate precise patterns of gene expression. While recent publications have described the importance of coordinated action of transcriptional activators at multiple cis-regulatory modules or enhancers, the contribution of sequence-specific repressors to overall regulation and robustness of gene expression has been difficult to ascertain. The Ets transcriptional repressor Yan functions as part of a conserved network downstream of receptor tyrosine kinase (RTK) signaling in Drosophila. This network displays switch-like responsiveness to RTK signaling, with the transition from a high-Yan to a low-Yan state induced by mitogen-activated protein kinase (MAPK)-mediated phosphorylation and inactivation of Yan. The ability of Yan to self-associate through a conserved sterile α motif (SAM) is essential for Yan's repressive ability, and has been suggested to allow spreading of Yan repressive complexes along chromatin. Such a mechanism has the potential to confer both signal responsiveness and robustness to the Yan network. To explore this spreading model, we compared the genome-wide chromatin binding profiles of wild-type vs. monomeric Yan. Consistent with the starting prediction, we found that wild type chromatin occupancy at genes encoding crucial developmental regulators and core signaling pathway components occurs as clusters of peaks that "spread" over multiple kilobases. However monomeric Yan, which fails to rescue a yan null mutation and displays significantly impaired repressive ability, exhibits a broadly similar occupancy profile to that of wild-type Yan, with multi-kilobase binding at developmentally important genes. This unexpected result suggests that SAM-mediated self-association does not mediate Yan recruitment to DNA or chromatin spreading, and raises the questions of why developmentally important genes require extensive Yan chromatin occupancy and how SAM-mediated polymerization might contribute to active repressive mechanisms in this context. In this Extra View article we discuss potential mechanisms by which Yan self-association and extended chromatin occupancy may contribute to robust regulation of gene expression.

Entities:  

Keywords:  ChIP; Drosophila; eye development; repressor; transcription

Mesh:

Substances:

Year:  2013        PMID: 23575308      PMCID: PMC3732337          DOI: 10.4161/fly.24162

Source DB:  PubMed          Journal:  Fly (Austin)        ISSN: 1933-6934            Impact factor:   2.160


  57 in total

1.  Ras pathway specificity is determined by the integration of multiple signal-activated and tissue-restricted transcription factors.

Authors:  M S Halfon; A Carmena; S Gisselbrecht; C M Sackerson; F Jiménez; M K Baylies; A M Michelson
Journal:  Cell       Date:  2000-09-29       Impact factor: 41.582

2.  Polymerization of the SAM domain of TEL in leukemogenesis and transcriptional repression.

Authors:  C A Kim; M L Phillips; W Kim; M Gingery; H H Tran; M A Robinson; S Faham; J U Bowie
Journal:  EMBO J       Date:  2001-08-01       Impact factor: 11.598

3.  Derepression by depolymerization; structural insights into the regulation of Yan by Mae.

Authors:  Feng Qiao; Haiyun Song; Chongwoo A Kim; Michael R Sawaya; Jacob B Hunter; Mari Gingery; Ilaria Rebay; Albert J Courey; James U Bowie
Journal:  Cell       Date:  2004-07-23       Impact factor: 41.582

4.  Negative control of photoreceptor development in Drosophila by the product of the yan gene, an ETS domain protein.

Authors:  Z C Lai; G M Rubin
Journal:  Cell       Date:  1992-08-21       Impact factor: 41.582

5.  The ETS-domain: a new DNA-binding motif that recognizes a purine-rich core DNA sequence.

Authors:  F D Karim; L D Urness; C S Thummel; M J Klemsz; S R McKercher; A Celada; C Van Beveren; R A Maki; C V Gunther; J A Nye
Journal:  Genes Dev       Date:  1990-09       Impact factor: 11.361

6.  Interaction of murine ets-1 with GGA-binding sites establishes the ETS domain as a new DNA-binding motif.

Authors:  J A Nye; J M Petersen; C V Gunther; M D Jonsen; B J Graves
Journal:  Genes Dev       Date:  1992-06       Impact factor: 11.361

7.  MAE, a dual regulator of the EGFR signaling pathway, is a target of the Ets transcription factors PNT and YAN.

Authors:  Pavithra Vivekanand; Tina L Tootle; Ilaria Rebay
Journal:  Mech Dev       Date:  2004-12       Impact factor: 1.882

8.  The relationship between long-range chromatin occupancy and polymerization of the Drosophila ETS family transcriptional repressor Yan.

Authors:  Jemma L Webber; Jie Zhang; Lauren Cote; Pavithra Vivekanand; Xiaochun Ni; Jie Zhou; Nicolas Nègre; Richard W Carthew; Kevin P White; Ilaria Rebay
Journal:  Genetics       Date:  2012-11-19       Impact factor: 4.562

9.  Mutations affecting segment number and polarity in Drosophila.

Authors:  C Nüsslein-Volhard; E Wieschaus
Journal:  Nature       Date:  1980-10-30       Impact factor: 49.962

10.  Native interface of the SAM domain polymer of TEL.

Authors:  Hoang H Tran; Chongwoo A Kim; Salem Faham; Marie-Claire Siddall; James U Bowie
Journal:  BMC Struct Biol       Date:  2002-08-22
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