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PMID: 20453063 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

CHD8 interacts with CHD7, a protein which is mutated in CHARGE syndrome.

Human molecular genetics ·Vol. 19 ·No. 14 ·2010-07-15 ·Pages 2858-66

Batsukh T, Pieper L, Koszucka AM, von Velsen N, Hoyer-Fender S, Elbracht M, Bergman JE, Hoefsloot LH, Pauli S

Abstract

CHARGE syndrome is an autosomal dominant disorder caused in about two-third of cases by mutations in the CHD7 gene. For other genetic diseases e.g. hereditary spastic paraplegia, it was shown that interacting partners are involved in the underlying cause of the disease. These data encouraged us to search for CHD7 binding partners by a yeast two-hybrid library screen and CHD8 was identified as an interacting partner. The result was confirmed by a direct yeast two-hybrid analysis, co-immunoprecipitation studies and by a bimolecular fluorescence complementation assay. To investigate the function of CHD7 missense mutations in the CHD7-CHD8 interacting area on the binding capacity of both proteins, we included three known missense mutations (p.His2096Arg, p.Val2102Ile and p.Gly2108Arg) and one newly identified missense mutation (p.Trp2091Arg) in the CHD7 gene and performed both direct yeast two-hybrid and co-immunoprecipitation studies. In the direct yeast two-hybrid system, the CHD7-CHD8 interaction was disrupted by the missense mutations p.Trp2091Arg, p.His2096Arg and p.Gly2108Arg, whereas in the co-immunoprecipitation studies disruption of the CHD7-CHD8 interaction by the mutations could not be observed. The results lead to the hypothesis that CHD7 and CHD8 proteins are interacting directly and indirectly via additional linker proteins. Disruption of the direct CHD7-CHD8 interaction might change the conformation of a putative large CHD7-CHD8 complex and could be a disease mechanism in CHARGE syndrome.

MeSH Terms
Abnormalities, Multiple/genetics,metabolism Choanal Atresia/complications,genetics,metabolism Coloboma/complications,genetics,metabolism DNA Helicases/genetics,metabolism DNA-Binding Proteins/genetics,metabolism Deafness/complications,congenital,genetics,metabolism Developmental Disabilities/complications,genetics,metabolism Ear/abnormalities HeLa Cells Heart Defects, Congenital/complications,genetics,metabolism Humans Mutation/physiology Protein Binding/genetics Protein Interaction Domains and Motifs/genetics,physiology Sexual Infantilism/complications,genetics,metabolism Syndrome Transcription Factors/metabolism Transfection Two-Hybrid System Techniques
Chemicals
CHD8 protein, human DNA-Binding Proteins Transcription Factors DNA Helicases CHD7 protein, human
Authors & Affiliations
9 authors, click to expand affiliations / ORCID
Batsukh Tserendulam
Institute of Human Genetics, University of Göttingen, 37073 Göttingen, Germany.
Pieper Lasse
Koszucka Anna M
von Velsen Nina
Hoyer-Fender Sigrid
Elbracht Miriam
Bergman Jorieke E H
Hoefsloot Lies H
Pauli Silke
Article Info
Journal
Human molecular genetics
Abbr.
Hum Mol Genet
ISSN
1460-2083
Published
2010-07-15
Epub
2010-00-07
Pages
2858-66
Language
English
Region
England
NLM ID
9208958
Subset
IM
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