Duchow Heather K, Brechbiel Jillian L, Chatterjee Seema, Gavis Elizabeth R
Department of Molecular Biology, Princeton University, Princeton, NJ 08544, USA.
Dev Biol. 2005 Jun 1;282(1):207-17. doi: 10.1016/j.ydbio.2005.03.025.
Developmental control of translation is frequently mediated by regulatory elements that reside within 3' untranslated regions (3' UTRs). Two stem-loops within the nanos 3' UTR translational control element (TCE) act independently to direct translational repression of maternal nanos mRNA in the ovary or embryo. We have previously shown that the nanos TCE can also function in select somatic sites. Using an ectopic expression screen, we now identify a new site of TCE function, the dorsal pouch epithelium. Analysis of TCE mutants reveals that TCE activity in the dorsal pouch does not depend on either of the stem-loops required for maternal TCE function, but instead requires a third feature-a sequence that closely matches the Bearded box, a regulatory motif found in the 3' UTRs of several Notch pathway genes. In addition, we identify pleiohomeotic mRNA as an endogenous candidate for regulation by Bearded box-like motifs in the dorsal pouch. Together, these results suggest that the TCE has appropriated a conserved regulatory motif to expand its function to somatic tissues.
翻译调控的发育控制通常由位于3'非翻译区(3'UTR)内的调控元件介导。nanos 3'UTR翻译控制元件(TCE)中的两个茎环独立发挥作用,指导卵巢或胚胎中母体nanos mRNA的翻译抑制。我们之前已经表明,nanos TCE也可以在特定的体细胞位点发挥作用。通过异位表达筛选,我们现在确定了TCE功能的一个新位点,即背袋上皮。对TCE突变体的分析表明,背袋中的TCE活性不依赖于母体TCE功能所需的任何一个茎环,而是需要第三个特征——一个与Bearded框紧密匹配的序列,Bearded框是在几个Notch通路基因的3'UTR中发现的调控基序。此外,我们将多同源异型mRNA鉴定为背袋中由Bearded框样基序调控的内源性候选物。总之,这些结果表明,TCE利用了一个保守的调控基序,将其功能扩展到体细胞组织。