Furnes Bjarte, Schimenti John
Department of Biomedical Sciences, College of Veterinary Medicine, Cornell University, T9014A, Ithaca, NY 14853, USA.
J Physiol. 2007 Jan 1;578(Pt 1):25-32. doi: 10.1113/jphysiol.2006.119164. Epub 2006 Sep 14.
The study of reproductive genetics in mammals has lagged behind that of simpler and more tractable model organisms, such as D. melanogaster, C. elegans and various yeast models. Although much valuable information has been generated using these organisms, they do not model the genetic and biological complexity of mammalian reproduction. Thus, the majority of genes required for gametogenesis in mammals remain unidentified. To expand on the existing knowledge of mammalian reproductive genetics, we have carried out forward genetic screens in mice to identify infertility mutants and the underlying mutant genes. Two different approaches were used: mutagenesis of the germline in whole mice, and mutagenesis of embryonic stem cells. This was followed by two- or three-generation breeding schemes to identify pedigrees segregating infertility mutations, which were then phenotypically characterized, genetically mapped, and in some cases, positionally cloned. This whole-genome approach has generated a wide collection of mutants with defects ranging from problems with germ cell development to abnormal sperm morphology. These models have allowed us to study the genetics, as well as the physiology, of reproduction in mammals. This review focuses on describing some of the genes identified in these screens and the ongoing effort to characterize additional mutants.
哺乳动物生殖遗传学的研究落后于果蝇、秀丽隐杆线虫和各种酵母模型等更简单、更易于处理的模式生物。尽管利用这些生物已经产生了许多有价值的信息,但它们无法模拟哺乳动物生殖的遗传和生物学复杂性。因此,哺乳动物配子发生所需的大多数基因仍未被鉴定出来。为了扩展哺乳动物生殖遗传学的现有知识,我们在小鼠中进行了正向遗传筛选,以鉴定不育突变体和潜在的突变基因。我们采用了两种不同的方法:对整个小鼠的生殖系进行诱变,以及对胚胎干细胞进行诱变。随后进行两到三代的育种方案,以鉴定分离不育突变的家系,然后对其进行表型特征分析、基因定位,在某些情况下还进行定位克隆。这种全基因组方法产生了大量具有各种缺陷的突变体,这些缺陷从生殖细胞发育问题到异常精子形态不等。这些模型使我们能够研究哺乳动物生殖的遗传学和生理学。本综述重点描述了在这些筛选中鉴定出的一些基因,以及表征其他突变体的持续努力。