Expression and function of the let-7 RNA in C. elegans

描述：22个核苷酸的let-7 RNA基因是新发现的非编码RNA基因大家族的创始成员，称为microRNAs (miRNAs)，似乎存在于所有多细胞生物中。通过遗传研究发现，秀丽隐杆线虫的let-7 RNA基因是一个重要的发育时间调节因子。let-7 RNA序列，参与其表达的蛋白质，包括RNA干扰（RNAi）途径中的参与者，以及由该RNA控制的基因在动物系统发育中广泛保守。本研究的长期目标是阐明let-7 RNA在秀丽隐杆线虫中的表达和功能，并期望这一发现将有助于揭示let-7在人类健康和发育中的作用。此外，本研究将有助于对新发现的miRNA基因大家庭的生物发生和目的的一般理解。为了验证let-7 RNA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剂的假设，将追求以下具体目标：1。描述产生22nt产物的let-7 RNA转录本的序列。(A)将确定let-7 RNA初级转录物和加工中间体的序列。(B)调节加工的let-7 RNA序列元件将通过体外分析与体内功能分析相结合来确定。2. 鉴定参与let-7 RNA表达的基因。(A)在前向遗传筛选中分离的突变，旨在鉴定与dcr-1（将大约70nt的pre- 7 RNA加工成22nt形式的RNase）一起起作用的基因，将被表征和鉴定。(B)含有核糖核酸酶、RNA解旋酶或RNA结合结构域的候选基因将通过在特定基因被RNAi灭活的提取物中进行加工反应来测试在let-7 RNA成熟中的作用。3. 确定介导特定靶标的依赖于let-7的调节的因子。(A)使用由let-7调节的敏感报告基因将发现与let-7 RNA一起起作用的基因。(B)与let-7调控的lin-41 3'UTR序列相关的因子将使用体外合成的RNA探针和秀丽隐杆线虫提取物进行表征。

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.