Chagnovich D, Lehmann R
Developmental Genetics Program, Skirball Institute of Biomolecular Medicine, New York University School of Medicine, and Howard Hughes Medical Institute, New York, NY 10016, USA.
Proc Natl Acad Sci U S A. 2001 Sep 25;98(20):11359-64. doi: 10.1073/pnas.201284398. Epub 2001 Sep 18.
Development of the Drosophila abdomen requires repression of maternal hunchback (hb) mRNA translation in the posterior of the embryo. This regulation involves at least four components: nanos response elements within the hb 3' untranslated region and the activities of Pumilio (PUM), Nanos (NOS), and Brain tumor. To study this regulation, we have developed an RNA injection assay that faithfully recapitulates the regulation of the endogenous hb message. Previous studies have suggested that NOS and PUM can regulate translation by directing poly(A) removal. We have found that RNAs that lack a poly(A) tail and cannot be polyadenylated and RNAs that contain translational activating sequences in place of the poly(A) tail are still repressed in the posterior. These data demonstrate that the poly(A) tail is not required for regulation and suggest that NOS and PUM can regulate hb translation by two mechanisms: removal of the poly(A) tail and a poly(A)-independent pathway that directly affects translation.
果蝇腹部的发育需要抑制胚胎后部母源驼背(hb)mRNA的翻译。这种调控至少涉及四个成分:hb 3'非翻译区内的纳米反应元件以及Pumilio(PUM)、Nanos(NOS)和脑肿瘤的活性。为了研究这种调控,我们开发了一种RNA注射试验,该试验能如实地重现内源性hb信息的调控。先前的研究表明,NOS和PUM可以通过指导聚腺苷酸的去除来调控翻译。我们发现,缺乏聚腺苷酸尾巴且不能被聚腺苷酸化的RNA,以及含有翻译激活序列代替聚腺苷酸尾巴的RNA,在后部仍然受到抑制。这些数据表明,聚腺苷酸尾巴对于调控不是必需的,并表明NOS和PUM可以通过两种机制调控hb翻译:去除聚腺苷酸尾巴和直接影响翻译的不依赖聚腺苷酸的途径。