Simon H G, Nelson C, Goff D, Laufer E, Morgan B A, Tabin C
Department of Genetics, Harvard Medical School, Boston, Massachusetts 02115.
Dev Dyn. 1995 Jan;202(1):1-12. doi: 10.1002/aja.1002020102.
An amputated limb of an adult urodele amphibian is capable of undergoing regeneration. The new structures form from an undifferentiated mass of cells called the regenerative blastema. The cells of the blastema are believed to derive from differentiated tissues of the adult limb. However, the exact source of these cells and the process by which they undergo dedifferentiation are poorly understood. In order to elucidate the molecular and cellular basis for dedifferentiation we isolated a number of genes which are potential regulators of the process. These include Msx-1, which is believed to support the undifferentiated and proliferative state of cells in the embryonic limb bud; and two members of the myogenic regulatory gene family, MRF-4 and Myf-5, which are expressed in differentiated muscle and regulate muscle-specific gene activity. As anticipated, we find that Msx-1 is strongly up-regulated during the initiation of regeneration. It remains expressed throughout regeneration but is not found in the fully regenerated limb. The myogenic gene MRF-4 has the reverse expression pattern. It is expressed in adult limb muscle, is rapidly shut off in early regenerative blastemas, and is only reexpressed at the completion of regeneration. These kinetics are paralleled by those of a muscle-specific Myosin gene. In contrast Myf-5, a second member of the myogenic gene family, continues to be expressed throughout the regenerative process. Thus, MRF-4 and Myf-5 are likely to play distinct roles during regeneration. MRF-4 may directly regulate muscle phenotype and as such its repression may be a key event in dedifferentiation.(ABSTRACT TRUNCATED AT 250 WORDS)
成年有尾两栖动物的断肢能够再生。新结构由一团未分化的细胞形成,称为再生芽基。芽基的细胞被认为来源于成年肢体的分化组织。然而,这些细胞的确切来源以及它们去分化的过程仍知之甚少。为了阐明去分化的分子和细胞基础,我们分离出了一些可能是该过程调节因子的基因。这些基因包括Msx-1,据信它能维持胚胎肢芽中细胞的未分化和增殖状态;以及肌源性调节基因家族的两个成员MRF-4和Myf-5,它们在分化的肌肉中表达并调节肌肉特异性基因的活性。正如预期的那样,我们发现Msx-1在再生开始时强烈上调。它在整个再生过程中持续表达,但在完全再生的肢体中未发现。肌源性基因MRF-4具有相反的表达模式。它在成年肢体肌肉中表达,在早期再生芽基中迅速关闭,仅在再生完成时重新表达。这些动力学与肌肉特异性肌球蛋白基因的动力学平行。相比之下,肌源性基因家族的另一个成员Myf-5在整个再生过程中持续表达。因此,MRF-4和Myf-5在再生过程中可能发挥不同的作用。MRF-4可能直接调节肌肉表型,因此其抑制可能是去分化中的关键事件。(摘要截短于250字)