Literature DB >> 15640247

CECR2, a protein involved in neurulation, forms a novel chromatin remodeling complex with SNF2L.

Graham S Banting1, Orr Barak, Tanya M Ames, Amanda C Burnham, Melanie D Kardel, Neil S Cooch, Courtney E Davidson, Roseline Godbout, Heather E McDermid, Ramin Shiekhattar.   

Abstract

Chromatin remodeling complexes play critical roles in development. Here we describe a transcription factor, CECR2, which is involved in neurulation and chromatin remodeling. CECR2 shows complex alternative splicing, but all variants contain DDT and bromodomain motifs. A mutant mouse line was generated from an embryonic stem cell line containing a genetrap within Cecr2. Reporter gene expression demonstrated Cecr2 expression to be predominantly neural in the embryo. Mice homozygous for the Cecr2 genetrap-induced mutation show a high penetrance of the neural tube defect exencephaly, the human equivalent of anencephaly, in a strain-dependent fashion. Biochemical isolation of CECR2 revealed the presence of this protein as a component of a novel heterodimeric complex termed CECR2-containing remodeling factor (CERF). CERF comprises CECR2 and the ATP-dependent chromatin remodeler SNF2L, a mammalian ISWI ortholog expressed predominantly in the central nervous system. CERF is capable of remodeling chromatin in vitro and displays an ATP hydrolyzing activity that is stimulated by nucleosomes. Together, these data identify a novel chromatin remodeling complex with a critical role in neurulation.

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Year:  2005        PMID: 15640247     DOI: 10.1093/hmg/ddi048

Source DB:  PubMed          Journal:  Hum Mol Genet        ISSN: 0964-6906            Impact factor:   6.150


  60 in total

1.  NMR Analyses of Acetylated H2A.Z Isoforms Identify Differential Binding Interactions with the Bromodomain of the NURF Nucleosome Remodeling Complex.

Authors:  Noelle M Olson; Samantha Kroc; Jorden A Johnson; Huda Zahid; Peter D Ycas; Alice Chan; Jennifer R Kimbrough; Prakriti Kalra; Ernst Schönbrunn; William C K Pomerantz
Journal:  Biochemistry       Date:  2020-05-11       Impact factor: 3.162

2.  Human ISWI chromatin-remodeling complexes sample nucleosomes via transient binding reactions and become immobilized at active sites.

Authors:  Fabian Erdel; Thomas Schubert; Caroline Marth; Gernot Längst; Karsten Rippe
Journal:  Proc Natl Acad Sci U S A       Date:  2010-10-25       Impact factor: 11.205

3.  A unique missense allele of BAF155, a core BAF chromatin remodeling complex protein, causes neural tube closure defects in mice.

Authors:  Laura Harmacek; Dawn E Watkins-Chow; Jianfu Chen; Kenneth L Jones; William J Pavan; J Michael Salbaum; Lee Niswander
Journal:  Dev Neurobiol       Date:  2014-01-09       Impact factor: 3.964

Review 4.  Dynamic regulation of lysine acetylation: the balance between acetyltransferase and deacetylase activities.

Authors:  Kelly A Hyndman; Mark A Knepper
Journal:  Am J Physiol Renal Physiol       Date:  2017-07-12

5.  Expansion of the ISWI chromatin remodeler family with new active complexes.

Authors:  Mariano Oppikofer; Tianyi Bai; Yutian Gan; Benjamin Haley; Peter Liu; Wendy Sandoval; Claudio Ciferri; Andrea G Cochran
Journal:  EMBO Rep       Date:  2017-08-11       Impact factor: 8.807

6.  GNE-886: A Potent and Selective Inhibitor of the Cat Eye Syndrome Chromosome Region Candidate 2 Bromodomain (CECR2).

Authors:  Terry D Crawford; James E Audia; Steve Bellon; Daniel J Burdick; Archana Bommi-Reddy; Alexandre Côté; Richard T Cummings; Martin Duplessis; E Megan Flynn; Michael Hewitt; Hon-Ren Huang; Hariharan Jayaram; Ying Jiang; Shivangi Joshi; James R Kiefer; Jeremy Murray; Christopher G Nasveschuk; Arianne Neiss; Eneida Pardo; F Anthony Romero; Peter Sandy; Robert J Sims; Yong Tang; Alexander M Taylor; Vickie Tsui; Jian Wang; Shumei Wang; Yongyun Wang; Zhaowu Xu; Laura Zawadzke; Xiaoqin Zhu; Brian K Albrecht; Steven R Magnuson; Andrea G Cochran
Journal:  ACS Med Chem Lett       Date:  2017-06-01       Impact factor: 4.345

7.  Functional genomics identifies therapeutic targets for MYC-driven cancer.

Authors:  Masafumi Toyoshima; Heather L Howie; Maki Imakura; Ryan M Walsh; James E Annis; Aaron N Chang; Jason Frazier; B Nelson Chau; Andrey Loboda; Peter S Linsley; Michele A Cleary; Julie R Park; Carla Grandori
Journal:  Proc Natl Acad Sci U S A       Date:  2012-05-23       Impact factor: 11.205

8.  The emerging role of epigenetic mechanisms in the etiology of neural tube defects.

Authors:  Nicholas D E Greene; Philip Stanier; Gudrun E Moore
Journal:  Epigenetics       Date:  2011-07-01       Impact factor: 4.528

9.  Partial tetrasomy of chromosome 22q11.1 resulting from a supernumerary isodicentric marker chromosome in a boy with cat-eye syndrome.

Authors:  Jung Min Ko; Jun Bum Kim; Ki Soo Pai; Jun-No Yun; Sang-Jin Park
Journal:  J Korean Med Sci       Date:  2010-11-24       Impact factor: 2.153

10.  Geminin loss causes neural tube defects through disrupted progenitor specification and neuronal differentiation.

Authors:  Ethan S Patterson; Laura E Waller; Kristen L Kroll
Journal:  Dev Biol       Date:  2014-07-01       Impact factor: 3.582

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