Expression and function of the let-7 RNA in C. elegans
Expression and function of the let-7 RNA in C. elegans
批准号:
6898275
负责人:
AMY E. PASQUINELLI
金额:
$26.91万
依托单位国家:
美国
项目类别:
财政年份:
2004
资助国家:
美国
项目状态:
已结题
起止时间:
2004-06-01 至 2009-05-31
关键词:
Caenorhabditis elegansRNARNA binding proteinRNA biosynthesisRNA interferenceendoribonucleasesgene expressiongene mutationgenetic regulationgenetic regulatory elementgenetic screeninghelicasenorthern blottingsnucleic acid probesnucleic acid quantitation /detectionnucleic acid sequencepolymerase chain reactionposttranscriptional RNA processing
中文摘要
描述:22个核苷酸的let-7RNA基因是一个新发现的称为microRNAs(MiRNAs)的非编码RNA基因大家族的创始成员,似乎存在于所有多细胞生物体中。在线虫中,let-7RNA基因是一种重要的发育调控因子,在线虫的遗传学研究中被发现。Let-7RNA序列、参与其表达的蛋白质,包括RNA干扰(RNAi)途径中的成员,以及由该RNA控制的基因在动物系统发育中广泛保守。这项建议的长期目标是阐明let-7 RNA在线虫中是如何表达和功能的,期望这一见解将有助于揭示let-7在人类健康和发育中的作用。此外,这项研究将有助于对新发现的miRNA基因这个庞大家族的生物发生和目的的总体理解。为了验证let-7RNA基因的表达和功能需要特定的RNA序列和蛋白质因子来产生这种发育调节因子的假设,将追求以下特定的目标:1.鉴定导致22nt产物的let-7RNA转录本的序列。(A)将确定let-7 RNA初级转录本和加工中间体的序列。(B)将通过将体外分析与体内功能分析相结合来确定调节加工的let-7 RNA序列元件。2.筛选与let-7RNA表达相关的基因。(A)在正向遗传筛查中分离的突变将被表征和鉴定,目的是识别与DCR-1功能相关的基因,DCR-1是一种将大约70nt的Pre-let-7RNA加工成22nt形式的RNase。(B)含有核糖核酸酶、RNA解旋酶或RNA结合域的候选基因将通过在特定基因被RNAi灭活的提取液中进行加工反应,来测试其在let-7 RNA成熟中的作用。3.确定介导let-7依赖的特定靶点调控的因素。(A)使用由let-7调控的敏感报告,将发现与let-7 RNA一起发挥作用的基因。(B)将使用体外合成的RNA探针和线虫提取物来表征因子与LET-7调控的LIN-41 3‘UTR序列的相关性。
英文摘要
DESCRIPTION: The 22 nucleotide let-7 RNA gene is a founding member of a large family of newly identified non-coding RNA genes, called microRNAs (miRNAs), which appear to be present in all multicellular organisms. The let-7 RNA gene was identified by genetic studies in the nematode Caenorhabditis elegans as an important regulator of developmental timing. The let-7 RNA sequence, proteins involved in its expression, including players in the RNA interference (RNAi) pathway, and genes controlled by this RNA are broadly conserved across animal phylogeny. The long-term goal of this proposal is to elucidate how the let-7 RNA is expressed and functions in C. elegans with the expectation that this insight will help reveal the role of let-7 in human health and development. Additionally, this research will contribute to the general understanding of the biogenesis and purpose of the populous family of newly discovered miRNA genes. To test the hypothesis that expression and function of the let-7 RNA gene requires specific RNA sequences and protein factors to produce this regulator of development, the following specific aims will be pursued: 1. Characterize the sequence of let-7 RNA transcripts that give rise to the 22nt product. (A) The sequence of the let-7 RNA primary transcript and processing intermediates will be determined. (B) The let-7 RNA sequence elements that regulate processing will be defined by coupling in vitro assays to in vivo functional analyses. 2. Identify genes involved in the expression of let-7 RNA. (A) Mutations isolated in a forward genetic screen aimed at identifying genes that function with dcr-1, the RNase that processes the approximate 70nt pre-let-7 RNA to the 22nt form, will be characterized and identified. (B) Candidate genes containing ribonuclease, RNA helicase or RNA binding domains will be tested for roles in let-7 RNA maturation by performing processing reactions in extracts where specific genes have been inactivated by RNAi. 3. Determine the factors that mediate let-7-dependent regulation of specific targets. (A) Genes that function with let-7 RNA will be uncovered using a sensitive reporter that is regulated by let-7. (B) The association of factors with the lin-41 3'UTR sequences regulated by let-7 will be characterized using in vitro synthesized RNA probes and C. elegans extracts.
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Biogenesis and Function of Regulatory RNAs
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