Watanabe Naoharu, Ishihara Takeshi, Ohshima Yasumi
Department of Biology, Faculty of Sciences, Kyushu University Graduate School, Hakozaki, Fukuoka 812-8581, Japan.
Genes Cells. 2007 May;12(5):603-9. doi: 10.1111/j.1365-2443.2007.01077.x.
Body size determination is critical for multicellular organisms; however, the mechanisms remain largely unknown. Mutations that alter body size were studied to solve the mechanisms, for example, in mouse, fruit fly and the nematode Caenorhabditis elegans. In C. elegans, a large mutant and several small body size (sma) mutants are known. Of the latter, sma-2, sma-3, sma-4, sma-6, dbl-1 and daf-4 have a mutation in the components of the DBL-1/TGFbeta signal pathway, and sma-5 in a MAP kinase homologue. We have constructed double mutants carrying two of such small body size mutations, sma-5 and sma-4 or sma-2. They are much smaller than either of the parental single mutants, indicating that the sma-5 gene functions independently of the DBL-1/TGFbeta pathway. We show that their body volumes are as small as 1/10 of that of the wild-type, and that the sizes of major organs are much reduced, by the methods previously developed by us. But the numbers of cells are not changed, suggesting that the cells are very small. These results highlight surprising flexibility of body size and cell size in a multicellular organism, which will give a novel insight into the mechanisms of body size control.
体型的确定对于多细胞生物至关重要;然而,其机制在很大程度上仍不为人知。人们通过研究改变体型的突变来解析这些机制,例如在小鼠、果蝇和线虫秀丽隐杆线虫中进行研究。在秀丽隐杆线虫中,已知有一个大体型突变体和几个小体型(sma)突变体。在后者中,sma - 2、sma - 3、sma - 4、sma - 6、dbl - 1和daf - 4在DBL - 1/TGFβ信号通路的组分中有突变,而sma - 5在一个MAP激酶同源物中有突变。我们构建了携带两个此类小体型突变(sma - 5和sma - 4或sma - 2)的双突变体。它们比任何一个亲本单突变体都小得多,这表明sma - 5基因的功能独立于DBL - 1/TGFβ通路。我们通过我们之前开发的方法表明,它们的身体体积小至野生型的1/10,并且主要器官的大小大幅减小。但是细胞数量没有改变,这表明细胞非常小。这些结果凸显了多细胞生物中体型和细胞大小惊人的灵活性,这将为体型控制机制提供新的见解。