THE DAZ GENES AND EARLY GERM CELL DEVELOPMENT

DAZ 基因和早期生殖细胞发育

• 批准号: 6181813
• 负责人: Renee A Reijo Pera
• 金额: $ 16.45万
• 依托单位: UNIVERSITY OF CALIFORNIA, SAN FRANCISCO
• 依托单位国家: 美国
• 财政年份: 1999
• 资助国家: 美国
• 起止时间: 1999-07-15 至 2004-06-30
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/6181813
• 关键词: RNA; RNA binding protein; chromosome deletion; clinical research; developmental genetics; embryogenesis; fertility; gene deletion mutation; gene expression; genetic mapping; germ cells; human genetic material tag; human subject; immunocytochemistry; immunoprecipitation; karyotype; male; nucleic acid sequence; phenotype; protein protein interaction; sex chromosomes; site directed mutagenesis; spermatogenesis; testis; yeast two hybrid system

Nearly five percent of men have defects in sperm production but are otherwise healthy. Our previous work led to identification of a common genetic cause of infertility in men, de novo deletions of the DAZ (Deleted in AZoospermia) region of the Y chromosome. Within this region, we identified a cluster of nearly-identical DAZ genes. Several lines of evidence suggest that this gene family is required for germ cell allocation or proliferation and maintenance of early germ cell populations. First, the protein expression pattern suggests an early function for DAZ and an autosomal homolog, DAZL, in all descendants of the germ lineage. Second, although men with deletions of the DAZ gene cluster produce very few sperm, those they do make are morphologically and physiologically normal which suggests DAZ-deleted men have a premeiotic defect in sperm production rather than a defect in spermiogenesis. Third, disruption of the DAZ gene homolog in mice causes infertility in both sexes and depletion of germ cells prenatally, well before meiosis. Finally, the Xenopus homolog of DAZ, X-Dazl, is expressed in the germ plasm, a region of the developing embryo that gives rise to the germ lineage in this organism. This investigation will use biochemical, genetic and molecular biological strategies to elucidate the mechanism by which the DAZ gene family insures that allocation or maintenance and proliferation of early germ cell populations occurs. Specifically, our aims over the next five years are to: 1) Identify and characterize the genes that encode protein(s) that interact with DAZ-protein, 2) identify and characterize the genes that encode RNA substrate(s) that interact with DAZ protein, and 3) identify and characterize other genes, with the same distinctive pattern of expression as exhibited by members of the DAZ gene family, using testicular biopsy tissues from men with different spermatogenic arrest phenotypes.

近5%的男性在精子生产方面有缺陷，但在其他方面是健康的。 我们以前的工作导致了男性不育的一个常见遗传原因的鉴定，Y染色体DAZ（AZoospermia中的DAZ）区域的从头缺失。 在这个区域内，我们发现了一组几乎相同的DAZ基因。 一些证据表明，该基因家族是生殖细胞分配或增殖和维持早期生殖细胞群体所必需的。首先，蛋白质表达模式表明DAZ和常染色体同源物DAZL在生殖谱系的所有后代中具有早期功能。 其次，尽管DAZ基因簇缺失的男性产生的精子很少，但他们产生的精子在形态和生理上都是正常的，这表明DAZ基因簇缺失的男性在精子产生方面存在减数分裂前缺陷，而不是精子发生缺陷。 第三，DAZ基因同源物在小鼠中的破坏导致两性不育和产前生殖细胞的耗尽，早在减数分裂之前。最后，DAZ的爪蟾同源物X-Dazl在生殖质中表达，生殖质是发育中的胚胎的一个区域，在这种生物体中产生生殖谱系。 这项研究将使用生物化学，遗传学和分子生物学策略来阐明DAZ基因家族确保早期生殖细胞群体的分配或维持和增殖的机制。 具体而言，我们在未来五年的目标是：1）鉴定和表征编码与DAZ蛋白相互作用的蛋白的基因，2）鉴定和表征编码与DAZ蛋白相互作用的RNA底物的基因，和3）鉴定和表征具有与DAZ基因家族成员所表现出的相同的独特表达模式的其他基因，使用来自具有不同生精停滞表型的男性的睾丸活检组织。