Farh Kyle Kai-How, Grimson Andrew, Jan Calvin, Lewis Benjamin P, Johnston Wendy K, Lim Lee P, Burge Christopher B, Bartel David P
Whitehead Institute for Biomedical Research, Department of Biology, Massachusetts Institute of Technology, and Howard Hughes Medical Institute, 9 Cambridge Center, Cambridge, MA 02142, USA.
Science. 2005 Dec 16;310(5755):1817-21. doi: 10.1126/science.1121158. Epub 2005 Nov 24.
Thousands of mammalian messenger RNAs are under selective pressure to maintain 7-nucleotide sites matching microRNAs (miRNAs). We found that these conserved targets are often highly expressed at developmental stages before miRNA expression and that their levels tend to fall as the miRNA that targets them begins to accumulate. Nonconserved sites, which outnumber the conserved sites 10 to 1, also mediate repression. As a consequence, genes preferentially expressed at the same time and place as a miRNA have evolved to selectively avoid sites matching the miRNA. This phenomenon of selective avoidance extends to thousands of genes and enables spatial and temporal specificities of miRNAs to be revealed by finding tissues and developmental stages in which messages with corresponding sites are expressed at lower levels.
数以千计的哺乳动物信使核糖核酸(mRNA)处于选择性压力之下,以维持与微小核糖核酸(miRNA)匹配的7个核苷酸位点。我们发现,这些保守的靶标在miRNA表达之前的发育阶段通常高度表达,并且随着靶向它们的miRNA开始积累,其水平往往会下降。数量比保守位点多10倍的非保守位点也介导抑制作用。因此,与miRNA在同一时间和地点优先表达的基因已经进化到选择性地避开与该miRNA匹配的位点。这种选择性避开现象延伸到数千个基因,并通过寻找其中具有相应位点的信使核糖核酸(mRNA)表达水平较低的组织和发育阶段,揭示了miRNA的空间和时间特异性。