Forry-Schaudies S, Maihle N J, Hughes S H
BRI-Basic Research Program, NCI-Frederick Cancer Research Facility, MD 21701.
J Mol Biol. 1990 Jan 20;211(2):321-30. doi: 10.1016/0022-2836(90)90354-O.
We have determined the organization of the chicken tropomyosin 1 gene by sequencing the cloned genomic DNA. The single-copy gene spans approximately 11,000 bases and includes 12 exons. Comparison of cDNA and genomic sequences demonstrates that three tissue-specific tropomyosins are encoded by the gene: a 284 amino acid skeletal muscle beta-tropomyosin, a 284 amino acid smooth muscle tropomyosin, and a 248 amino acid non-muscle (fibroblast) beta-tropomyosin. Skeletal and smooth muscle transcripts use the same putative promoter and transcription initiation site. However, they are alternatively spliced to generate mRNAs that differ in the region giving rise to amino acids 188 to 213 and 258 through the poly(A) site. The fibroblast transcript uses a promoter, initiation site and first exon that is distinct from that used for both the smooth and the skeletal muscle transcripts. However, beyond the first exon the fibroblast transcript undergoes splicing and polyadenylation that is identical with the smooth muscle transcript.
我们通过对克隆的基因组DNA进行测序,确定了鸡原肌球蛋白1基因的结构。这个单拷贝基因跨度约11000个碱基,包含12个外显子。cDNA与基因组序列的比较表明,该基因编码三种组织特异性原肌球蛋白:一种由284个氨基酸组成的骨骼肌β-原肌球蛋白、一种由284个氨基酸组成的平滑肌原肌球蛋白,以及一种由248个氨基酸组成的非肌肉(成纤维细胞)β-原肌球蛋白。骨骼肌和平滑肌转录本使用相同的假定启动子和转录起始位点。然而,它们通过可变剪接产生的mRNA在对应氨基酸188至213以及258到poly(A)位点的区域有所不同。成纤维细胞转录本使用的启动子、起始位点和第一个外显子与平滑肌和骨骼肌转录本所使用的不同。不过,在第一个外显子之后,成纤维细胞转录本的剪接和聚腺苷酸化过程与平滑肌转录本相同。