Allen Robert S, Li Junyan, Stahle Melissa I, Dubroué Aurélie, Gubler Frank, Millar Anthony A
School of Biochemistry and Molecular Biology, Australian National University, Canberra ACT 0200, Australia.
Proc Natl Acad Sci U S A. 2007 Oct 9;104(41):16371-6. doi: 10.1073/pnas.0707653104. Epub 2007 Oct 4.
Currently, there are very few loss-of-function mutations in micro-RNA genes. Here, we characterize two members of the Arabidopsis MIR159 family, miR159a and miR159b, that are predicted to regulate the expression of a family of seven transcription factors that includes the two redundant GAMYB-like genes, MYB33 and MYB65. Using transfer DNA (T-DNA) insertional mutants, we show that a mir159ab double mutant has pleiotropic morphological defects, including altered growth habit, curled leaves, small siliques, and small seeds. Neither mir159a nor mir159b single mutants displayed any of these traits, indicating functional redundancy. By using reporter-gene constructs, it appears that MIR159a and MIR159b are transcribed almost exclusively in the cells in which MYB33 is repressed, as had been previously determined by comparison of MYB33 and mMYB33 (an miR159-resistant allele of MYB33) expression patterns. Consistent with these overlapping transcriptional domains, MYB33 and MYB65 expression levels were elevated throughout mir159ab plants. By contrast, the other five GAMYB-like family members are transcribed predominantly in tissues where miR159a and miR159b are absent, and consequently their expression levels are not markedly elevated in mir159ab. Additionally, mMYB33 transgenic plants can phenocopy the mir159ab phenotype, suggesting that its phenotype is explained by deregulated expression of the redundant gene pair MYB33 and MYB65. This prediction was confirmed; the pleiotropic developmental defects of mir159ab are suppressed through the combined mutations of MYB33 and MYB65, demonstrating the narrow and specific target range of miR159a and miR159b.
目前,微小RNA基因中的功能丧失突变非常少。在这里,我们对拟南芥MIR159家族的两个成员miR159a和miR159b进行了表征,预计它们会调控一个包含七个转录因子的家族的表达,其中包括两个冗余的类GAMYB基因MYB33和MYB65。利用转移DNA(T-DNA)插入突变体,我们发现mir159ab双突变体具有多效性形态缺陷,包括生长习性改变、叶片卷曲、角果小和种子小。mir159a和mir159b单突变体均未表现出这些性状,表明存在功能冗余。通过使用报告基因构建体,似乎MIR159a和MIR159b几乎只在MYB33被抑制的细胞中转录,正如之前通过比较MYB33和mMYB33(MYB33的一个抗miR159等位基因)的表达模式所确定的那样。与这些重叠的转录域一致,MYB33和MYB65在整个mir159ab植株中的表达水平升高。相比之下,其他五个类GAMYB家族成员主要在不存在miR159a和miR159b的组织中转录,因此它们在mir159ab中的表达水平没有明显升高。此外,mMYB33转基因植株可以模拟mir159ab的表型,表明其表型是由冗余基因对MYB33和MYB65的表达失调所解释的。这一预测得到了证实;mir159ab的多效性发育缺陷通过MYB33和MYB65的联合突变得到抑制,证明了miR159a和miR159b的狭窄且特定的靶标范围。