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PMID: 14660547 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

The pro-apoptotic gene Bax is required for the death of ectopic primordial germ cells during their migration in the mouse embryo.

Development (Cambridge, England) ·Vol. 130 ·No. 26 ·2003-12-00 ·Pages 6589-97

Stallock J, Molyneaux K, Schaible K, Knudson CM, Wylie C

Abstract

In the mouse embryo, significant numbers of primordial germ cells (PGCs) fail to migrate correctly to the genital ridges early in organogenesis. These usually die in ectopic locations. In humans, 50% of pediatric germ line tumors arise outside the gonads, and these are thought to arise from PGCs that fail to die in ectopic locations. We show that the pro-apoptotic gene Bax, previously shown to be required for germ cell death during later stages of their differentiation in the gonads, is also expressed during germ cell migration, and is required for the normal death of germ cells left in ectopic locations during and after germ cell migration. In addition, we show that Bax is downstream of the known cell survival signaling interaction mediated by the Steel factor/Kit ligand/receptor interaction. Together, these observations identify the major mechanism that removes ectopic germ cells from the embryo at early stages.

MeSH Terms
Animals Apoptosis/genetics Cell Death Cell Movement Cell Survival Choristoma/embryology,genetics Embryonic and Fetal Development/genetics Female Gene Expression Regulation, Developmental/genetics Green Fluorescent Proteins Luminescent Proteins/genetics Male Mice Mice, Transgenic Organ Culture Techniques Ovum/physiology Proto-Oncogene Proteins/genetics Proto-Oncogene Proteins c-bcl-2 Spermatozoa/physiology bcl-2-Associated X Protein
Chemicals
Bax protein, mouse Luminescent Proteins Proto-Oncogene Proteins Proto-Oncogene Proteins c-bcl-2 bcl-2-Associated X Protein Green Fluorescent Proteins
Authors & Affiliations
5 authors, click to expand affiliations / ORCID
Stallock James
Division of Developmental Biology, Cincinnati Children's Hospital Research Foundation, Cincinnati, OH 45229, USA.
Molyneaux Kathy
Schaible Kyle
Knudson C Michael
Wylie Christopher
Article Info
Journal
Development (Cambridge, England)
Abbr.
Development
ISSN
0950-1991
Published
2003-12-00
Pages
6589-97
Language
English
Region
England
NLM ID
8701744
Subset
IM
Grants
NICHD NIH HHS · 1 F32 HD008678-01 · United States
NCI NIH HHS · 1R01CA88967 · United States
NICHD NIH HHS · R01 HD33440 · United States
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