Genetic rescue of follicle-stimulating hormone β-deficient mice

被引:79
作者
Kumar, TR
Low, MJ
Matzuk, MM
机构
[1] Baylor Coll Med, Dept Pathol, Houston, TX 77030 USA
[2] Baylor Coll Med, Dept Cell Biol, Houston, TX 77030 USA
[3] Baylor Coll Med, Dept Mol & Human Genet, Houston, TX 77030 USA
[4] Oregon Hlth & Sci Univ, Vollum Inst, Portland, OR 97201 USA
关键词
D O I
10.1210/en.139.7.3289
中图分类号
R5 [内科学];
学科分类号
1002 [临床医学]; 100201 [内科学];
摘要
FSH is an alpha:beta heterodimeric pituitary glycoprotein that shares a common alpha-subunit with LH and TSH. To study the role of FSH in mammalian reproduction, we have previously generated an FSH-deficient mouse model using embryonic stem (ES) cell technology by introducing a null mutation in the unique FSH beta gene. Male mice deficient in FSH are fertile despite their small testes and reduced sperm number and motility. In contrast, FSK-deficient female mice are infertile due to a block in folliculogenesis at the preantral stage. In this set of experiments, we have rescued the mutant phenotypes of FSH beta-deficient mice by two genetic strategies. In the type I rescue mice, we introduced into the FSH beta-deficient background a 10-kb human FSH beta transgene that is selectively expressed in pituitary gonadotropes. The presence of this transgene [and thus the interspecies hybrid (i.e. mouse cu:human FSH beta hormone)] in the background of mouse FSH beta deficiency completely restored the testis size, sperm number, and motility defects to levels comparable to those seen in control male mice. AU of the mouse FSH beta-deficient female mice carrying this human FSH beta transgene resumed normal folliculogenesis, were fertile and delivered normal size Litters. In the type II rescue mice, human FSH (human alpha:human FSH beta) was ectopically produced from multiple tissues in the mutant background using a mouse metallothionein-I promoter. Whereas ectopic production of human FSH completely rescued the mouse FSH beta-deficient male mice, only 3 out of 10 mouse FSH beta-deficient females bearing these human FSH transgenes were fertile and carried their pregnancies to term and parturition. We conclude that the resultant phenotypes due to a genetic deficiency of mouse FSH beta can be corrected by appropriate expression of human FSH transgenes and that human FSH beta gene regulation and function in the mouse pituitary are indistinguishable from the endogenous mouse FSH beta gene.
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收藏
页码:3289 / 3295
页数:7
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