Alpha-fetoprotein, the major fetal serum protein, is not essential for embryonic development but is required for female fertility
Author(s) -
Philippe Gabant,
Lesley M. Forrester,
Jennifer Nichols,
Thierry Van Reeth,
Christelle De Mees,
Bernard Pajack,
Alistair J. Watt,
Johan Smitz,
Henri Alexandre,
Claude Szpirer,
Josiane Szpirer
Publication year - 2002
Publication title -
proceedings of the national academy of sciences
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 5.011
H-Index - 771
eISSN - 1091-6490
pISSN - 0027-8424
DOI - 10.1073/pnas.202215399
Subject(s) - biology , anovulation , embryo , embryogenesis , gene , vitamin d binding protein , andrology , fetus , endocrinology , medicine , albumin , genetics , embryonic stem cell , pregnancy , vitamin d and neurology , insulin resistance , polycystic ovary , insulin
The alpha-fetoprotein gene (Afp) is a member of a multigenic family that comprises the related genes encoding albumin, alpha-albumin, and vitamin D binding protein. The biological role of this major embryonic serum protein is unknown although numerous speculations have been made. We have used gene targeting to show that AFP is not required for embryonic development. AFP null embryos develop normally, and individually transplanted homozygous embryos can develop in an AFP-deficient microenvironment. Whereas mutant homozygous adult males are viable and fertile, AFP null females are infertile. Our analyses of these mice indicate that the defect is caused by a dysfunction of the hypothalamic/pituitary system, leading to anovulation.
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