Weydert A, Daubas P, Lazaridis I, Barton P, Garner I, Leader D P, Bonhomme F, Catalan J, Simon D, Guénet J L
Proc Natl Acad Sci U S A. 1985 Nov;82(21):7183-7. doi: 10.1073/pnas.82.21.7183.
Myosin heavy chain (MHC) genes are expressed as several distinct isoforms in a tissue- and stage-specific manner; three skeletal muscle MHC isoforms appear sequentially during development. We have isolated cDNA clones, identified by RNA blot hybridization and by nucleotide sequence determination as coding for portions of the embryonic (pMHC2.2), perinatal (pMHC16.2A), and alpha(V1) cardiac (pMHC141 and pMHC101) MHC isoforms. These four probes and the adult skeletal MHC probe (pMHC32) have been used on Southern blots of genomic DNA to detect restriction fragment length polymorphisms defining the alleles for these genes in mouse species Mus musculus and Mus spretus. In this way, we followed the segregation of skeletal and cardiac MHC genes in 42 offspring resulting from an interspecies backcross. We found that the embryonic, perinatal, and adult skeletal MHC genes are clustered on chromosome 11 near the locus nude, the skeletal and cardiac MHC genes do not cosegregate, and the alpha(V1) cardiac MHC gene is located on chromosome 14 close to Np-1. This result is in contrast to that for other contractile protein genes such as the alkali myosin light chain and the actin multigene families, which are dispersed in the genome.
肌球蛋白重链(MHC)基因以组织和阶段特异性的方式表达为几种不同的异构体;三种骨骼肌MHC异构体在发育过程中依次出现。我们已经分离出cDNA克隆,通过RNA印迹杂交和核苷酸序列测定鉴定其编码胚胎(pMHC2.2)、围产期(pMHC16.2A)和α(V1)心脏(pMHC141和pMHC101)MHC异构体的部分序列。这四种探针和成年骨骼肌MHC探针(pMHC32)已用于基因组DNA的Southern印迹分析,以检测定义小家鼠和西班牙小鼠这两个小鼠物种中这些基因等位基因的限制性片段长度多态性。通过这种方式,我们追踪了种间回交产生的42只后代中骨骼肌和心脏MHC基因的分离情况。我们发现,胚胎、围产期和成年骨骼肌MHC基因在11号染色体上靠近裸基因座的位置聚集,骨骼肌和心脏MHC基因不共分离,α(V1)心脏MHC基因位于14号染色体上靠近Np-1的位置。这一结果与其他收缩蛋白基因如碱性肌球蛋白轻链和肌动蛋白多基因家族的情况形成对比,后者在基因组中是分散的。