Achanzar W E, Ward S
Department of Molecular and Cellular Biology, The University of Arizona, Tucson 85721, USA.
J Cell Sci. 1997 May;110 ( Pt 9):1073-81. doi: 10.1242/jcs.110.9.1073.
During maturation of spermatids to motile spermatozoa in Caenorhabditis elegans, large vesicles called membranous organelles (MOs) fuse with the spermatid plasma membrane. Mutations in the gene fer-1 cause abnormal spermatozoa in which the MOs do not fuse, although they abut the plasma membrane normally. Here we describe the fer-1 gene, which we found to be approximately 8.6 kb in length and to encode a 6.2 kb transcript whose expression is limited to the primary spermatocytes, the cells in which the MOs form. fer-1 is predicted to encode a 235 kDa protein which is highly charged except for a putative transmembrane domain near the C terminus. We identified the mutations associated with five fer-1 alleles, all of which are missense mutations causing single amino acid changes. FER-1 is not similar to any characterized proteins in sequence databases, nor does it contain known functional motifs other than the predicted transmembrane domain. The C-terminal transmembrane domain makes FER-1 resemble some viral fusion proteins, suggesting it may play a direct role in MO-plasma membrane fusion. FER-1 does show significant sequence similarity to several predicted human proteins of unknown function. Two of the identified fer-1 mutations are located in regions of similarity between FER-1 and two of these predicted proteins. This strengthens the biological significance of these similarities and suggests these regions of similarity represent functionally important domains of FER-1 and the human proteins.
在秀丽隐杆线虫精子细胞成熟为可游动精子的过程中,称为膜性细胞器(MOs)的大囊泡与精子细胞质膜融合。fer - 1基因的突变会导致精子异常,其中MOs不发生融合,尽管它们通常与质膜相邻。在这里,我们描述了fer - 1基因,我们发现其长度约为8.6 kb,编码一个6.2 kb的转录本,其表达仅限于初级精母细胞,即MOs形成的细胞。fer - 1预计编码一个235 kDa的蛋白质,除了C末端附近一个假定的跨膜结构域外,该蛋白质带大量电荷。我们鉴定了与五个fer - 1等位基因相关的突变,所有这些都是错义突变,导致单个氨基酸变化。FER - 1在序列数据库中与任何已鉴定的蛋白质都不相似,除了预测的跨膜结构域外,它也不包含已知的功能基序。C末端跨膜结构域使FER - 1类似于一些病毒融合蛋白,表明它可能在MO - 质膜融合中起直接作用。FER - 1确实与几种功能未知的预测人类蛋白质显示出显著的序列相似性。已鉴定的两个fer - 1突变位于FER - 1与其中两种预测蛋白质的相似区域。这加强了这些相似性的生物学意义,并表明这些相似区域代表了FER - 1和人类蛋白质的功能重要结构域。