Frail D E, Mudd J, Shah V, Carr C, Cohen J B, Merlie J P
Proc Natl Acad Sci U S A. 1987 Sep;84(17):6302-6. doi: 10.1073/pnas.84.17.6302.
Postsynaptic membranes isolated from Torpedo electric organ are highly enriched in the nicotinic acetylcholine receptor and a nonreceptor protein of 43 kDa; the distribution of the 43-kDa protein and the receptor is coextensive in the electrical membrane. As a first step in understanding the regulation of 43-kDa protein expression, we have isolated and characterized 43-kDa protein cDNAs. A lambda gt11 cDNA library was constructed from Torpedo californica electric organ mRNA and screened with a pool of 26-mer oligonucleotides encoding a short tryptic fragment of the 43-kDa synaptic protein. Positive clones were purified and sequenced; the amino acid sequences were deduced, and they matched chemically determined protein sequences of the 43-kDa protein. Two distinct classes of cDNAs were obtained; one class encoded a 43-kDa protein of 389 amino acids with a calculated molecular mass of 43,988 daltons, and another class encoded a second 43-kDa protein containing 23 additional amino acids at the C terminus. Therefore, it appears that two 43-kDa proteins with different carboxyl termini are encoded by separate mRNAs. Consistent with this idea, blot hybridization analysis revealed multiple polyadenylylated 43-kDa mRNAs in electric organ. One polyadenylylated mRNA of approximately equal to 2.0 kilobases in length was apparent in both embryonic day-11 chick muscle and the mouse muscle cell line BC3H1.
从电鳐电器官分离出的突触后膜富含烟碱型乙酰胆碱受体和一种43 kDa的非受体蛋白;在电膜中,43 kDa蛋白和该受体的分布是共延的。作为了解43 kDa蛋白表达调控的第一步,我们分离并鉴定了43 kDa蛋白的cDNA。用来自加州电鳐电器官mRNA构建了一个λgt11 cDNA文库,并用一组编码43 kDa突触蛋白短胰蛋白酶片段的26聚体寡核苷酸进行筛选。阳性克隆被纯化并测序;推导了氨基酸序列,它们与化学测定的43 kDa蛋白的蛋白质序列相匹配。获得了两类不同的cDNA;一类编码一个由389个氨基酸组成、计算分子量为43,988道尔顿的43 kDa蛋白,另一类编码第二个43 kDa蛋白,其C末端含有另外23个氨基酸。因此,似乎两个具有不同羧基末端的43 kDa蛋白由不同的mRNA编码。与此观点一致,印迹杂交分析显示电器官中有多个多聚腺苷酸化的43 kDa mRNA。在胚胎第11天的鸡肌肉和小鼠肌肉细胞系BC3H1中都出现了一种长度约为2.0千碱基的多聚腺苷酸化mRNA。