Literature DB >> 33127760

CHD7 regulates cardiovascular development through ATP-dependent and -independent activities.

Shun Yan1, Rassarin Thienthanasit1, Dongquan Chen2, Erik Engelen3, Joanna Brühl3, David K Crossman1, Robert Kesterson1, Qin Wang4, Karim Bouazoune5, Kai Jiao6.   

Abstract

CHD7 encodes an ATP-dependent chromatin remodeling factor. Mutation of this gene causes multiple developmental disorders, including CHARGE (Coloboma of the eye, Heart defects, Atresia of the choanae, Retardation of growth/development, Genital abnormalities, and Ear anomalies) syndrome, in which conotruncal anomalies are the most prevalent form of heart defects. How CHD7 regulates conotruncal development remains unclear. In this study, we establish that deletion of Chd7 in neural crest cells (NCCs) causes severe conotruncal defects and perinatal lethality, thus providing mouse genetic evidence demonstrating that CHD7 cell-autonomously regulates cardiac NCC development, thereby clarifying a long-standing controversy in the literature. Using transcriptomic analyses, we show that CHD7 fine-tunes the expression of a gene network that is critical for cardiac NCC development. To gain further molecular insights into gene regulation by CHD7, we performed a protein-protein interaction screen by incubating recombinant CHD7 on a protein array. We find that CHD7 directly interacts with several developmental disorder-mutated proteins including WDR5, a core component of H3K4 methyltransferase complexes. This direct interaction suggested that CHD7 may recruit histone-modifying enzymes to target loci independently of its remodeling functions. We therefore generated a mouse model that harbors an ATPase-deficient allele and demonstrates that mutant CHD7 retains the ability to recruit H3K4 methyltransferase activity to its targets. Thus, our data uncover that CHD7 regulates cardiovascular development through ATP-dependent and -independent activities, shedding light on the etiology of CHD7-related congenital disorders. Importantly, our data also imply that patients carrying a premature stop codon versus missense mutations will likely display different molecular alterations; these patients might therefore require personalized therapeutic interventions.

Entities:  

Keywords:  CHARGE syndrome; CHD7; cardiac neural crest cells; cardiovascular development; nucleosome remodeling

Mesh:

Substances:

Year:  2020        PMID: 33127760      PMCID: PMC7682373          DOI: 10.1073/pnas.2005222117

Source DB:  PubMed          Journal:  Proc Natl Acad Sci U S A        ISSN: 0027-8424            Impact factor:   11.205


  77 in total

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7.  Chd7 cooperates with Sox10 and regulates the onset of CNS myelination and remyelination.

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Authors:  Corentine Marie; Adrien Clavairoly; Magali Frah; Hatem Hmidan; Jun Yan; Chuntao Zhao; Juliette Van Steenwinckel; Romain Daveau; Bernard Zalc; Bassem Hassan; Jean-Léon Thomas; Pierre Gressens; Philippe Ravassard; Ivan Moszer; Donna M Martin; Q Richard Lu; Carlos Parras
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  8 in total

1.  Drp1 regulates transcription of ribosomal protein genes in embryonic hearts.

Authors:  Qiancong Zhao; Shun Yan; Jin Lu; Danitra J Parker; Huiying Wu; Qianchuang Sun; David K Crossman; Shanrun Liu; Qin Wang; Hiromi Sesaki; Kasturi Mitra; Kexiang Liu; Kai Jiao
Journal:  J Cell Sci       Date:  2022-02-21       Impact factor: 5.285

Review 2.  Epigenetic Regulation of Cardiac Neural Crest Cells.

Authors:  Shun Yan; Jin Lu; Kai Jiao
Journal:  Front Cell Dev Biol       Date:  2021-04-21

Review 3.  Semaphorin Regulation by the Chromatin Remodeler CHD7: An Emerging Genetic Interaction Shaping Neural Cells and Neural Crest in Development and Cancer.

Authors:  Antonella Lettieri; Roberto Oleari; Alyssa J J Paganoni; Cristina Gervasini; Valentina Massa; Alessandro Fantin; Anna Cariboni
Journal:  Front Cell Dev Biol       Date:  2021-04-01

Review 4.  The Cardiac Neural Crest Cells in Heart Development and Congenital Heart Defects.

Authors:  Shannon Erhardt; Mingjie Zheng; Xiaolei Zhao; Tram P Le; Tina O Findley; Jun Wang
Journal:  J Cardiovasc Dev Dis       Date:  2021-07-30

5.  CHD7 in oocytes is essential for female fertility.

Authors:  Jie Cheng; Qian Dong; Yujia Lu; Liya Shi; Guangxin Yao; Chaojun Wang; Cheng Zhou; Zhaoming Zhou; Zhuxi Huang; Ziang Han; Ming Zhu; Weijun Feng
Journal:  Ann Transl Med       Date:  2022-03

6.  Characterization of Two Mouse Chd7 Heterozygous Loss-of-Function Models Shows Dysgenesis of the Corpus Callosum and Previously Unreported Features of CHARGE Syndrome.

Authors:  Stephan C Collins; Valerie E Vancollie; Anna Mikhaleva; Christel Wagner; Rebecca Balz; Christopher J Lelliott; Binnaz Yalcin
Journal:  Int J Mol Sci       Date:  2022-09-29       Impact factor: 6.208

Review 7.  Eyes on CHARGE syndrome: Roles of CHD7 in ocular development.

Authors:  Laura A Krueger; Ann C Morris
Journal:  Front Cell Dev Biol       Date:  2022-09-08

Review 8.  Sentinels of chromatin: chromodomain helicase DNA-binding proteins in development and disease.

Authors:  Andrej Alendar; Anton Berns
Journal:  Genes Dev       Date:  2021-11-01       Impact factor: 11.361

  8 in total

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