Baldwin T J, Yoshihara C M, Blackmer K, Kintner C R, Burden S J
Biology Department, Massachusetts Institute of Technology, Cambridge 02139.
J Cell Biol. 1988 Feb;106(2):469-78. doi: 10.1083/jcb.106.2.469.
The level of transcripts encoding the skeletal muscle acetylcholine receptor (AChR) was determined during embryonic development in Xenopus laevis. cDNAs encoding the alpha, gamma, and delta subunits of the Xenopus AChR were isolated from Xenopus embryo cDNA libraries using Torpedo AChR cDNAs as probes. The Xenopus AChR cDNAs have greater than 60% amino acid sequence homology to their Torpedo homologues and hybridize to transcripts that are restricted to the somites of developing embryos. Northern blot analysis demonstrates that a 2.3-kb transcript hybridizes to the alpha subunit cDNA, a 2.4-kb transcript hybridizes to the gamma subunit cDNA, and that two transcripts, of 1.9 and 2.5 kb, hybridize to the delta subunit cDNA. RNase protection assays demonstrate that transcripts encoding alpha, gamma, and delta subunits are coordinately expressed at late gastrula and that the amount of each transcript increases in parallel with muscle-specific actin mRNA during the ensuing 12 h. After the onset of muscle activity the level of actin mRNA per somite remains relatively constant, whereas the level of alpha subunit and delta subunit transcripts decrease fourfold per somite and the level of gamma subunit transcript decreases greater than 50-fold per somite. The decrease in amount of AChR transcripts per somite, however, occurs when embryos are paralyzed with local anaesthetic during their development. These results demonstrate that AChR transcripts in Xenopus are initially expressed coordinately, but that gamma subunit transcript levels are regulated differently than alpha and delta at later stages. Moreover, these results demonstrate that AChR transcript levels in Xenopus myotomal muscle cells are not responsive to electrical activity and suggest that AChR transcript levels are influenced by other regulatory controls.
在非洲爪蟾胚胎发育过程中,测定了编码骨骼肌乙酰胆碱受体(AChR)的转录本水平。利用电鳐AChR的cDNA作为探针,从非洲爪蟾胚胎cDNA文库中分离出编码非洲爪蟾AChR的α、γ和δ亚基的cDNA。非洲爪蟾AChR的cDNA与其电鳐同源物的氨基酸序列同源性大于60%,并与发育中胚胎体节特有的转录本杂交。Northern印迹分析表明,一个2.3 kb的转录本与α亚基cDNA杂交,一个2.4 kb的转录本与γ亚基cDNA杂交,两个1.9 kb和2.5 kb的转录本与δ亚基cDNA杂交。核糖核酸酶保护分析表明,编码α、γ和δ亚基的转录本在原肠胚晚期协同表达,并且在随后的12小时内,每个转录本的量与肌肉特异性肌动蛋白mRNA平行增加。肌肉活动开始后,每个体节的肌动蛋白mRNA水平保持相对恒定,而α亚基和δ亚基转录本的水平每个体节下降四倍,γ亚基转录本的水平每个体节下降超过50倍。然而,每个体节AChR转录本数量的减少发生在胚胎发育过程中用局部麻醉剂使其麻痹时。这些结果表明,非洲爪蟾中的AChR转录本最初是协同表达的,但在后期γ亚基转录本水平的调节与α和δ亚基不同。此外,这些结果表明,非洲爪蟾肌节肌细胞中的AChR转录本水平对电活动无反应,并表明AChR转录本水平受其他调节控制的影响。