Wilson Luke D, Obakpolor Omoyemwen A, Jones Autumn M, Richie Abigail L, Mieczkowski Bryce D, Fall Gabriel T, Hall Rosine W, Rumbley Jon N, Kroft Tim L
Department of Anatomic Pathology, Mayo Clinic, Rochester, Minnesota.
Department of Biology, College of Sciences, Auburn University at Montgomery, Montgomery, Alabama.
Mol Reprod Dev. 2018 Jul;85(7):563-578. doi: 10.1002/mrd.22992. Epub 2018 May 23.
Fertilization, the fusion of sperm and oocyte to form a zygote, is the first and arguably the most important cell-cell interaction event in an organism's life. Forward and reverse genetic approaches in the nematode Caenorhabditis elegans have identified many genes that are required for gametogenesis and fertilization and thus are beginning to elucidate the molecular pathways that underlie these processes. We identified an allele of the spe-49 gene in a second filial generation (F ) mutagenesis screen for spermatogenesis-defective (spe) mutants. Mutant worms for spe-49 produce sperm that have normal morphology, activate to form ameboid spermatozoa, and can migrate to and maintain their position in the hermaphrodite reproductive tract but fail to fertilize oocytes. This phenotype puts spe-49 in the spe-9 class of late-acting genes that function in sperm at the time of fertilization. We cloned the spe-49 gene through a combination of deficiency mapping, transgenic rescue, and genomic sequencing. spe-49 messenger RNA (mRNA) is enriched in male germ cells, and the complementary DNA (cDNA) encodes a predicted 772-amino-acid six-pass transmembrane protein that is homologous to SPE-42. Indeed, SPE-49 and SPE-42 have identical predicted membrane topology and domain structure, including a large extracellular domain with six conserved cysteine residues, a DC-STAMP domain, and a C-terminal cytoplasmic domain containing a C4-C4 RING finger motif. The presence of two SPE-42 homologs in animal genomes from worms to humans suggests that these proteins are highly conserved components of the molecular apparatus required for the sperm-oocyte recognition, binding, and fusion.
受精是精子与卵母细胞融合形成受精卵的过程,是生物体生命中首个且可说是最重要的细胞间相互作用事件。线虫秀丽隐杆线虫中的正向和反向遗传学方法已鉴定出许多配子发生和受精所需的基因,从而开始阐明这些过程背后的分子途径。我们在第二代(F₂)诱变筛选中鉴定出spe-49基因的一个等位基因,该筛选针对精子发生缺陷(spe)突变体。spe-49突变体蠕虫产生的精子具有正常形态,可激活形成阿米巴样精子,并且能够迁移到雌雄同体生殖道并维持其位置,但无法使卵母细胞受精。这种表型使spe-49属于spe-9类晚期作用基因,这些基因在受精时在精子中起作用。我们通过缺失图谱分析、转基因拯救和基因组测序相结合的方法克隆了spe-49基因。spe-49信使核糖核酸(mRNA)在雄性生殖细胞中富集,互补脱氧核糖核酸(cDNA)编码一个预测的772个氨基酸的六次跨膜蛋白,该蛋白与SPE-42同源。实际上,SPE-49和SPE-42具有相同的预测膜拓扑结构和结构域结构,包括一个带有六个保守半胱氨酸残基的大细胞外结构域、一个DC-STAMP结构域以及一个包含C4-C4环指基序的C末端细胞质结构域。从蠕虫到人类的动物基因组中存在两种SPE-42同源物,这表明这些蛋白质是精子-卵母细胞识别、结合和融合所需分子装置的高度保守组成部分。