کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
5531905 | 1401819 | 2017 | 9 صفحه PDF | دانلود رایگان |
- 3â² UTR of cebp-1 mRNA contains multiple regulatory elements.
- A stem-loop like structure regulates cebp-1's translation in neurons.
- Distinct 3â² UTR elements contributes to cebp-1 function in a context-dependent manner.
- Multiple mechanisms control optimization of cebp-1 expression levels.
The 3â² untranslated regions (3â² UTRs) of mRNAs mediate post-transcriptional regulation of genes in many biological processes. Cis elements in 3â² UTRs can interact with RNA-binding factors in sequence-specific or structure-dependent manners, enabling regulation of mRNA stability, translation, and localization. Caenorhabditis elegans CEBP-1 is a conserved transcription factor of the C/EBP family, and functions in diverse contexts, from neuronal development and axon regeneration to organismal growth. Previous studies revealed that the levels of cebp-1 mRNA in neurons depend on its 3â² UTR and are also negatively regulated by the E3 ubiquitin ligase RPM-1. Here, by systematically dissecting cebp-1's 3â² UTR, we test the roles of specific cis elements in cebp-1 expression and function in neurons. We present evidence for a putative stem-loop in the cebp-1 3â² UTR that contributes to basal expression levels of mRNA and to negative regulation by rpm-1. Mutant animals lacking the endogenous cebp-1 3â² UTR showed a noticeable increased expression of cebp-1 mRNA and enhanced the neuronal developmental phenotypes of rpm-1 mutants. Our data reveal multiple cis elements within cebp-1's 3â² UTR that help to optimize CEBP-1 expression levels in neuronal development.
Journal: Developmental Biology - Volume 429, Issue 1, 1 September 2017, Pages 240-248