Honda S, Epstein H F
Department of Neurology, Baylor College of Medicine, Houston, TX 77030.
Proc Natl Acad Sci U S A. 1990 Feb;87(3):876-80. doi: 10.1073/pnas.87.3.876.
The body-wall muscle cells of the nematode Caenorhabditis elegans produce thick filaments during embryonic, larval, and adult stages. These thick filaments contain two myosin isoforms, A and B, which assemble into different zones along the 10-microns lengths. Paramyosin, a protein homologous to myosin rods, forms a substratum for the myosins. The three filament proteins are encoded by different genes: myo-3 V (myosin heavy chain A), unc-54 I (myosin heavy chain B), and unc-15 I (paramyosin). The relative expression of these genes has been studied by run-on nuclear transcription in vitro, hybridization of accumulated mRNA, and immunochemical determination of specific polypeptide accumulation. In late larval nematodes (L4), the relative levels of nuclear run-on transcription per mol of probe are 6.4 unc-54:2.4 myo-3:1.0 unc-15. Similarly, the relative levels of immunospecific proteins are 4.5 unc-15:3.1 unc-54:1.0 myo-3. Most strikingly, the relative mRNA amounts are 50.0 unc-54:12.4 unc-15:1.0 myo-3. Thus, the orders of relative abundance and the quantitative relations of expression of the three functionally related genes change from transcriptional activities to final accumulated product of thick filament proteins. Modulation of the expression appears to involve processes affecting accumulation of mRNA and protein. The great difference in accumulation of the mRNAs for the two myosin heavy chain isoforms A and B may be related to the different roles of the myosins in thick filament assembly.
线虫秀丽隐杆线虫的体壁肌肉细胞在胚胎期、幼虫期和成虫期都会产生粗肌丝。这些粗肌丝包含两种肌球蛋白异构体,A和B,它们沿着10微米的长度组装到不同的区域。副肌球蛋白,一种与肌球蛋白杆同源的蛋白质,为肌球蛋白形成了一个基质。这三种丝蛋白由不同的基因编码:myo - 3 V(肌球蛋白重链A)、unc - 54 I(肌球蛋白重链B)和unc - 15 I(副肌球蛋白)。通过体外核转录延伸、积累的mRNA杂交以及特定多肽积累的免疫化学测定,对这些基因的相对表达进行了研究。在幼虫晚期线虫(L4)中,每摩尔探针的核转录延伸相对水平为6.4 unc - 54:2.4 myo - 3:1.0 unc - 15。同样,免疫特异性蛋白的相对水平为4.5 unc - 15:3.1 unc - 54:1.0 myo - 3。最显著的是,相对mRNA量为50.0 unc - 54:12.4 unc - 15:1.0 myo - 3。因此,这三个功能相关基因的相对丰度顺序和表达的定量关系从转录活性转变为粗肌丝蛋白的最终积累产物。表达的调节似乎涉及影响mRNA和蛋白质积累的过程。两种肌球蛋白重链异构体A和B的mRNA积累的巨大差异可能与肌球蛋白在粗肌丝组装中的不同作用有关。