Noël P, Cartwright I L
Department of Molecular Genetics, Biochemistry and Microbiology, University of Cincinnati College of Medicine, OH 45267-0524.
EMBO J. 1994 Nov 15;13(22):5253-61. doi: 10.1002/j.1460-2075.1994.tb06859.x.
The isolation and characterization of a Drosophila melanogaster gene (Dtrp1) that encodes a protein displaying the properties of both a structural and functional homolog of the yeast endoplasmic reticulum membrane-bound translocation protein Sec62p is reported. We show that Dtrp1 can not only rescue the lethality associated with a SEC62 gene knockout in yeast, but also complement the sec62-associated defective transport of a precursor polypeptide from the cytoplasm into the lumen of the endoplasmic reticulum. Expression of the Dtrp1 gene throughout Drosophila development is characterized by peaks in mid-embryo-genesis and mid-pupation, followed by a sustained period of mRNA accumulation in adults. The examination of male reproductive tissues showed a very high level of preferential expression of a 1.6 kb message, while a 2.2 kb message was confined almost exclusively to the non-reproductive tissues. Within the reproductive tract itself the 1.6 kb message was expressed in testes, ejaculatory duct and particularly strongly in the paragonial glands. Since these latter organs are specialized secretory tissues we suggest that the 1.6 kb message may encode a protein isoform that performs a unique, tissue-specific role in the protein translocation pathway. Such observations may indicate a hitherto unexpected diversity in components of the protein translocation pathway in respect to stage, tissue and, potentially, substrate specificity.
报道了黑腹果蝇基因(Dtrp1)的分离和特性,该基因编码一种蛋白质,其兼具酵母内质网膜结合易位蛋白Sec62p的结构和功能同源物的特性。我们发现,Dtrp1不仅能挽救酵母中与SEC62基因敲除相关的致死性,还能弥补sec62相关的前体多肽从细胞质到内质网腔的运输缺陷。Dtrp1基因在果蝇整个发育过程中的表达特征是在胚胎中期和化蛹中期出现峰值,随后在成虫中mRNA持续积累。对雄性生殖组织的检测显示,一种1.6 kb的信使RNA有非常高的优先表达水平,而一种2.2 kb的信使RNA几乎只局限于非生殖组织。在生殖道本身,1.6 kb的信使RNA在睾丸、射精管中表达,在副性腺中表达尤为强烈。由于后一种器官是专门的分泌组织,我们认为1.6 kb的信使RNA可能编码一种在蛋白质易位途径中发挥独特的组织特异性作用的蛋白质异构体。这些观察结果可能表明,在蛋白质易位途径的组成成分方面,在阶段、组织以及潜在的底物特异性方面存在迄今未预料到的多样性。