首页> 美国卫生研究院文献>Proceedings of the National Academy of Sciences of the United States of America >Genes for skeletal muscle myosin heavy chains are clustered and are not located on the same mouse chromosome as a cardiac myosin heavy chain gene.
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Genes for skeletal muscle myosin heavy chains are clustered and are not located on the same mouse chromosome as a cardiac myosin heavy chain gene.

机译:骨骼肌肌球蛋白重链的基因聚集在一起与心脏肌球蛋白重链基因不在同一小鼠染色体上。

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摘要

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.
机译:肌球蛋白重链(MHC)基因以组织和阶段特异性方式表达为几种不同的同工型。在发育过程中,三个骨骼肌MHC亚型依次出现。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为编码部分胚胎(pMHC2.2),围产期(pMHC16.2A)和alpha(V1)心脏(pMHC141和pMHC101)MHC亚型。这四种探针和成年骨骼MHC探针(pMHC32)已用于基因组DNA的Southern印迹中,以检测限制性片段长度多态性,这些片段限定了小鼠小家鼠和家鼠中这些基因的等位基因。通过这种方式,我们追踪了由种间回交产生的42个后代中骨骼和心脏MHC基因的分离。我们发现胚胎,围生期和成年骨骼MHC基因聚集在靠近裸鼠位点的第11号染色体上,骨骼和心脏MHC基因不共聚,而alpha(V1)心脏MHC基因位于靠近Np的第14号染色体上-1。该结果与分散在基因组中的其他可收缩蛋白基因(例如碱性肌球蛋白轻链和肌动蛋白多基因家族)相反。

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