Song W K, Wang W, Foster R F, Bielser D A, Kaufman S J
Department of Cell and Structural Biology, University of Illinois, Urbana 61801.
J Cell Biol. 1992 May;117(3):643-57. doi: 10.1083/jcb.117.3.643.
H36 is a 120,000-D membrane glycoprotein that is expressed during the differentiation of skeletal muscle. H36 cDNA clones were isolated from a lambda UniZapXR rat myotube cDNA library and sequenced. The deduced amino acid sequence demonstrates that H36 is a novel integrin alpha chain that shares extensive homology with other alpha integrins that includes: (a) the GFFKR sequence found in all alpha integrins; (b) a single membrane spanning region; (c) conservation of 18 of 22 cysteines; and (d) a protease cleavage site found in the non-I region integrin alpha chains. The cytoplasmic domain of H36 is unique and additional regions of nonhomology further indicate H36 is distinct from all other alpha chains. In keeping with current nomenclature we designate this alpha chain alpha 7. Northern blots demonstrate that expression of H36-alpha 7 mRNA is regulated both early in the development of the myogenic lineage and later, during terminal differentiation. Detection of H36-alpha 7 mRNA coincides with conversion of H36- myogenic precursor cells to H36+ cells. H36-alpha 7 mRNA is present in replicating myoblasts: expression increases upon terminal differentiation and is markedly reduced in developmentally defective myoblasts. In addition, H36-alpha 7 mRNA is not detected in C3H10T1/2 cells. It is in myotubes derived from myoblasts obtained by treatment of 10T1/2 cells with azacytidine or transfection with MRF4. Immunoblots and immunofluorescence demonstrate that the H36-alpha 7 chain is associated with integrin beta 1. Affinity chromatography demonstrates that H36-alpha 7 beta 1 selectively binds to laminin. The expression of H36-alpha 7 on secondary myoblasts during the development of the limb in vivo corresponds with the appearance of laminin in the limb, with the responsiveness of secondary myoblast proliferation to laminin, and with the onset of increased muscle mass, suggesting that H36-alpha 7 modulates this stage in limb development. We conclude that H36-alpha 7 is a novel alpha integrin laminin binding protein whose expression is developmentally regulated during skeletal myogenesis.
H36是一种分子量为120,000的膜糖蛋白,在骨骼肌分化过程中表达。从λUniZapXR大鼠肌管cDNA文库中分离出H36 cDNA克隆并进行测序。推导的氨基酸序列表明,H36是一种新型整合素α链,与其他α整合素具有广泛的同源性,包括:(a) 在所有α整合素中发现的GFFKR序列;(b) 一个单一的跨膜区域;(c) 22个半胱氨酸中有18个保守;(d) 在非I区域整合素α链中发现的蛋白酶切割位点。H36的胞质结构域是独特的,其他非同源区域进一步表明H36与所有其他α链不同。按照当前的命名法,我们将此α链命名为α7。Northern印迹显示,H36-α7 mRNA的表达在肌源性谱系发育早期和后期终末分化过程中均受到调控。H36-α7 mRNA的检测与H36-肌源性前体细胞向H36+细胞的转化一致。H36-α7 mRNA存在于增殖的成肌细胞中:在终末分化时表达增加,而在发育缺陷的成肌细胞中明显减少。此外,在C3H10T1/2细胞中未检测到H36-α7 mRNA。在用氮杂胞苷处理10T1/2细胞或用MRF4转染获得的成肌细胞衍生的肌管中可检测到。免疫印迹和免疫荧光表明,H36-α7链与整合素β1相关。亲和层析表明,H36-α7β1选择性结合层粘连蛋白。体内肢体发育过程中,次级成肌细胞上H36-α7的表达与肢体中层粘连蛋白的出现、次级成肌细胞增殖对层粘连蛋白的反应以及肌肉质量增加的开始相对应,这表明H36-α7调节肢体发育的这一阶段。我们得出结论,H36-α7是一种新型的α整合素层粘连蛋白结合蛋白,其表达在骨骼肌生成过程中受到发育调控。