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Targeted disruption of semaphorin 3C leads to persistent truncus arteriosus and aortic arch interruption
Author(s) -
Leonard Feiner,
Andrea L. Webber,
Christopher B. Brown,
Min Lü,
Jia Li,
Paul Feinstein,
Peter Mombaerts,
Jonathan A. Epstein,
Jonathan A. Raper
Publication year - 2001
Publication title -
development
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 3.754
H-Index - 325
eISSN - 1477-9129
pISSN - 0950-1991
DOI - 10.1242/dev.128.16.3061
Subject(s) - semaphorin , biology , truncus arteriosus , neural crest , microbiology and biotechnology , phenotype , plexin , anatomy , heart development , mutant , crest , embryo , medicine , genetics , embryonic stem cell , gene , tetralogy of fallot , heart disease , receptor , physics , quantum mechanics
Semaphorin 3C is a secreted member of the semaphorin gene family. To investigate its function in vivo, we have disrupted the semaphorin 3Clocus in mice by targeted mutagenesis. semaphorin 3C mutant mice die within hours after birth from congenital cardiovascular defects consisting of interruption of the aortic arch and improper septation of the cardiac outflow tract. This phenotype is similar to that reported following ablation of the cardiac neural crest in chick embryos and resembles congenital heart defects seen in humans. Semaphorin 3C is expressed in the cardiac outflow tract as neural crest cells migrate into it. Their entry is disrupted in semaphorin 3C mutant mice. These data suggest that semaphorin 3C promotes crest cell migration into the proximal cardiac outflow tract.

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