Lees-Miller J P, Goodwin L O, Helfman D M
Cold Spring Harbor Laboratory, New York 11724.
Mol Cell Biol. 1990 Apr;10(4):1729-42. doi: 10.1128/mcb.10.4.1729-1742.1990.
cDNA clones encoding three novel tropomyosins, termed TMBr-1, TMBr-2, and TMBr-3, were isolated and characterized from a rat brain cDNA library. All are derived from a single gene, which was previously found to express striated muscle alpha-tropomyosin and a number of other tropomyosin isoforms via an alternative splicing mechanism (N. Ruiz-Opazo and B. Nadal-Ginard, J. Biol. Chem. 262:4755-4765, 1987; D. F. Wieczorek, C. W. J. Smith, and B. Nadal-Ginard, Mol. Cell. Biol. 8:679-694, 1988). The derived amino acid sequences revealed that TMBr-1 contains 281 amino acids, TMBr-2 contains 251 amino acids, and TMBr-3 contains 245 amino acids. All three proteins contain a region that is identical to amino acids 81 through 258 of skeletal muscle alpha-tropomyosin. TMBr-1 is identical to striated muscle alpha-tropomyosin from amino acids 1 through 258 but contains a novel COOH-terminal region from amino acids 259 through 281. TMBr-2 and TMBr-3 both contain identical NH2-terminal sequences from amino acids 1 through 44 which were found to be expressed from a novel promoter. TMBr-3 contains the same COOH-terminal region as TMBr-1, whereas TMBr-2 contains a second novel COOH-terminal region. The genomic organization of the exons encoding TMBr-1, TMBr-2, and TMBr-3 were determined. These studies revealed a previously uncharacterized promoter located in the internal region of the alpha-TM gene as well as two novel COOH-terminal coding exons. The alpha-TM gene is a complex transcription unit containing 15 exons including two alternative promoters, two internal mutually exclusive exon cassettes, and four alternatively spliced 3' exons that encode four different COOH-terminal coding regions. A total of nine distinct mRNAs are known to be expressed from the alpha-TM gene in a cell type-specific manner in tissues such as striated muscle, smooth muscle, kidney, liver, brain, and fibroblasts. The mRNAs encoding TMBr-1, TMBr-2, and TMBr-3 were found to be expressed only in brain tissue, with TMBr-3 being expressed at much greater levels than TMBr-1 and TMBr-2. The individual structural characteristics of each brain alpha-tropomyosin isoform and their possible functions are discussed.
从大鼠脑cDNA文库中分离并鉴定了编码三种新型原肌球蛋白的cDNA克隆,分别命名为TMBr-1、TMBr-2和TMBr-3。它们均源自单个基因,该基因先前被发现通过可变剪接机制表达横纹肌α-原肌球蛋白和许多其他原肌球蛋白异构体(N. Ruiz-Opazo和B. Nadal-Ginard,《生物化学杂志》262:4755 - 4765,1987;D. F. Wieczorek、C. W. J. Smith和B. Nadal-Ginard,《分子细胞生物学》8:679 - 694,1988)。推导的氨基酸序列显示,TMBr-1含有281个氨基酸,TMBr-2含有251个氨基酸,TMBr-3含有245个氨基酸。这三种蛋白质均含有一个与骨骼肌α-原肌球蛋白第81至258位氨基酸相同的区域。TMBr-1在第1至258位氨基酸与横纹肌α-原肌球蛋白相同,但在第259至281位氨基酸含有一个新的COOH末端区域。TMBr-2和TMBr-3在第1至44位氨基酸均含有相同的NH2末端序列,该序列由一个新的启动子表达。TMBr-3与TMBr-1含有相同的COOH末端区域,而TMBr-2含有第二个新的COOH末端区域。确定了编码TMBr-1、TMBr-2和TMBr-3的外显子的基因组组织。这些研究揭示了位于α-TM基因内部区域的一个先前未鉴定的启动子以及两个新的COOH末端编码外显子。α-TM基因是一个复杂的转录单位,包含15个外显子,包括两个可变启动子、两个内部相互排斥的外显子盒以及四个可变剪接的3'外显子,它们编码四个不同的COOH末端编码区域。已知共有九种不同的mRNA以细胞类型特异性方式在横纹肌、平滑肌、肾脏、肝脏、大脑和成纤维细胞等组织中从α-TM基因表达。发现编码TMBr-1、TMBr-2和TMBr-3的mRNA仅在脑组织中表达,其中TMBr-3的表达水平远高于TMBr-1和TMBr-2。讨论了每种脑原肌球蛋白异构体的个体结构特征及其可能的功能。