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miRNA 和 Hox 基因之间的负反馈调控环控制秀丽隐杆线虫的后体身份。

A negative regulatory loop between microRNA and Hox gene controls posterior identities in Caenorhabditis elegans.

机构信息

Department of Genome Sciences, University of Washington, Seattle, Washington, United States of America.

出版信息

PLoS Genet. 2010 Sep 2;6(9):e1001089. doi: 10.1371/journal.pgen.1001089.

DOI:10.1371/journal.pgen.1001089
PMID:20824072
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2932687/
Abstract

MicroRNAs (miRNAs) have been found to regulate gene expression across eukaryotic species, but the function of most miRNA genes remains unknown. Here we describe how the analysis of the expression patterns of a well-conserved miRNA gene, mir-57, at cellular resolution for every minute during early development of Caenorhabditis elegans provided key insights in understanding its function. Remarkably, mir-57 expression shows strong positional bias but little tissue specificity, a pattern reminiscent of Hox gene function. Despite the minor defects produced by a loss of function mutation, overexpression of mir-57 causes dramatic posterior defects, which also mimic the phenotypes of mutant alleles of a posterior Hox gene, nob-1, an Abd homolog. More importantly, nob-1 expression is found in the same two posterior AB sublineages as those expressing mir-57 but with an earlier onset. Intriguingly, nob-1 functions as an activator for mir-57 expression; it is also a direct target of mir-57. In agreement with this, loss of mir-57 function partially rescues the nob-1 allele defects, indicating a negative feedback regulatory loop between the miRNA and Hox gene to provide positional cues. Given the conservation of the miRNA and Hox gene, the regulatory mechanism might be broadly used across species. The strategy used here to explore mir-57 function provides a path to dissect the regulatory relationship between genes.

摘要

微小 RNA(miRNAs)已被发现可在真核生物物种中调节基因表达,但大多数 miRNA 基因的功能仍然未知。在这里,我们描述了如何通过分析秀丽隐杆线虫早期发育过程中每分钟每个细胞 miRNA 基因 mir-57 的表达模式,深入了解其功能。值得注意的是,mir-57 的表达表现出强烈的位置偏向性,但组织特异性很小,这种模式类似于 Hox 基因的功能。尽管功能丧失突变产生的缺陷较小,但 mir-57 的过表达会导致严重的后向缺陷,这也模拟了后向 Hox 基因 nob-1(Abd 同源物)突变等位基因的表型。更重要的是,nob-1 表达在与 mir-57 表达相同的两个后 AB 亚谱系中,但起始时间更早。有趣的是,nob-1 作为 mir-57 表达的激活剂发挥作用;它也是 mir-57 的直接靶标。与这一致的是,缺失 mir-57 功能部分挽救了 nob-1 等位基因缺陷,表明 miRNA 和 Hox 基因之间存在负反馈调节环,以提供位置线索。鉴于 miRNA 和 Hox 基因的保守性,该调控机制可能在广泛的物种中使用。这里用于探索 mir-57 功能的策略为剖析基因之间的调控关系提供了一种途径。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fbbc/2932687/b8bd4a169c4c/pgen.1001089.g009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fbbc/2932687/1cf38463efc2/pgen.1001089.g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fbbc/2932687/5f083d98b0da/pgen.1001089.g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fbbc/2932687/1f23092d0e43/pgen.1001089.g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fbbc/2932687/969162189c3e/pgen.1001089.g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fbbc/2932687/571dfc5263fa/pgen.1001089.g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fbbc/2932687/2b1d21e890a7/pgen.1001089.g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fbbc/2932687/b58cd32cc132/pgen.1001089.g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fbbc/2932687/20fdad7578ee/pgen.1001089.g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fbbc/2932687/b8bd4a169c4c/pgen.1001089.g009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fbbc/2932687/1cf38463efc2/pgen.1001089.g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fbbc/2932687/5f083d98b0da/pgen.1001089.g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fbbc/2932687/1f23092d0e43/pgen.1001089.g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fbbc/2932687/969162189c3e/pgen.1001089.g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fbbc/2932687/571dfc5263fa/pgen.1001089.g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fbbc/2932687/2b1d21e890a7/pgen.1001089.g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fbbc/2932687/b58cd32cc132/pgen.1001089.g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fbbc/2932687/20fdad7578ee/pgen.1001089.g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fbbc/2932687/b8bd4a169c4c/pgen.1001089.g009.jpg

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