Department of Biology, Graduate School of Science, Kobe University, 1-1 Rokkodaicho, Nada-Ku, Kobe 657-8501, Japan.
Evol Dev. 2013 Jul-Aug;15(4):293-304. doi: 10.1111/ede.12039.
microRNAs (miRs) are small non-coding RNA molecules expressed in a tissue-specific manner in numerous organisms. Among them, miR-1, miR-206, and miR-133, which are encoded as bicistronic gene clusters in the genome, play major roles in the control of vertebrate myogenesis. To address how the gene organization and function of these miRs evolved, we identified their homologues in the cyclostomes, the chondrichthyans and the teleosts, and examined their patterns of expression during development. It was suggested that the chondrichthyans and the cyclostome lampreys possess fewer miR-1/miR-133 genes than the medaka. The medaka additionally possessed the miR-206 gene which was not found in the genomes of chondrichthyans and lampreys. In contrast, the number and genomic organization of medaka miR-1(206)/miR-133 were similar to those found in mammals. In the lamprey, shark and medaka, miR-1 and miR-133 were expressed in both skeletal and cardiac muscle cells in adults, a developmental feature traced back to chordate invertebrates such as ascidians. We further examined the expression of these miRs in different muscle tissues in medaka embryos. miR-206 was expressed in both the tail and pectoral fin muscles, whereas miR-1, which shares the similar nucleotide sequence with miR-206, was not detectable in the embryonic pectoral fins. Comparison of the relative positions with the neighboring protein-coding genes showed high conservation of synteny between the miR-1(206)/miR-133 clusters in a single species, as well as across the vertebrate taxa. Our results suggest that, after the gene duplications, these muscle-specific miRs acquired differential regulatory functions and have contributed to the establishment of diverse and complex musculature of vertebrates.
微小 RNA(miRs)是一类在许多生物体中以组织特异性方式表达的小非编码 RNA 分子。其中,miR-1、miR-206 和 miR-133 作为基因组中的双顺反子基因簇,在脊椎动物肌发生的调控中发挥重要作用。为了解这些 miR 的基因组织和功能是如何进化的,我们在圆口类、软骨鱼类和硬骨鱼类中鉴定了它们的同源物,并在发育过程中检测了它们的表达模式。结果表明,软骨鱼类和圆口类七鳃鳗比日本青鳉拥有更少的 miR-1/miR-133 基因。日本青鳉还拥有 miR-206 基因,而软骨鱼类和七鳃鳗的基因组中没有发现该基因。相比之下,日本青鳉 miR-1(206)/miR-133 的数量和基因组组织与哺乳动物相似。在七鳃鳗、鲨鱼和日本青鳉中,miR-1 和 miR-133 在成年的骨骼肌和心肌细胞中均有表达,这是一种从无脊椎动物如尾索动物追溯到脊索动物的发育特征。我们进一步检测了这些 miR 在日本青鳉胚胎不同肌肉组织中的表达。miR-206 在尾部和胸鳍肌肉中均有表达,而与 miR-206 具有相似核苷酸序列的 miR-1 在胚胎胸鳍中无法检测到。与邻近的蛋白质编码基因的相对位置比较表明,单个物种中 miR-1(206)/miR-133 簇之间以及整个脊椎动物类群之间的同线性高度保守。我们的结果表明,这些肌肉特异性 miR 在基因复制后获得了不同的调节功能,并为脊椎动物多样化和复杂的肌肉结构的建立做出了贡献。