魚類肌肉結構性蛋白:T型肌鈣蛋白(Troponin T)的分子結構、胚胎表現及基因調控﹝2/2﹞
Date Issued
2003-07-31
Date
2003-07-31
Author(s)
蔡懷楨
DOI
912313B002289
Abstract
Troponin T (Tnnt), a troponin component, interacts with tropomyosin and is crucial to the regulation of striated muscle
contraction. To gain insight into the molecular evolution and developmental regulation of Tnnt gene (Tnnt) in lower
vertebrates, zebrafish Tnnt1 (slow Tnnt), Tnnt2 (cardiac Tnnt), and Tnnt3b (fast Tnnt isoform b) were characterized.
The polypeptides of zebrafish Tnnt1, Tnnt2, and Tnnt3b were conserved in the central tropomyosin- and C-terminal
troponin I-binding domains. However, the N-terminal hypervariable regions were highly extended and rich in glutamic
acid in polypeptides of Tnnt1 and Tnnt2, but not Tnnt3b. The Tnnt2 and Tnnt3b contain introns, whereas Tnnt1 is
intron-free. During development, large to small, alternatively spliced variants were detected in Tnnt2, but not in Tnnt1
or Tnnt3. Whole-mount in situ hybridization showed zebrafish Tnnt1 and Tnnt2 are activated during early
somitogenesis (10 hr postfertilization, hpf) and cardiogenesis (14 hpf), respectively, but Tnnt3b is not activated until
middle somitogenesis (18 hpf). Tnnt2 and Tnnt3b expression was cardiac- and fast-muscle specific, but Tnnt1 was
expressed in both slow and fast muscles. We propose that three, distinct, muscle-type Tnnt evolved after the
divergence of fish and deuterostome invertebrates. In zebrafish, the developmental regulation of Tnnt during
somitogenesis and cardiogenesis is more restricted and simpler than in tetrapods. These new findings may provide
insight into the developmental regulation and molecular evolution of vertebrate Tnnt. Developmental Dynamics 227:
266–279, 2003. © 2003 Wiley-Liss, Inc.
contraction. To gain insight into the molecular evolution and developmental regulation of Tnnt gene (Tnnt) in lower
vertebrates, zebrafish Tnnt1 (slow Tnnt), Tnnt2 (cardiac Tnnt), and Tnnt3b (fast Tnnt isoform b) were characterized.
The polypeptides of zebrafish Tnnt1, Tnnt2, and Tnnt3b were conserved in the central tropomyosin- and C-terminal
troponin I-binding domains. However, the N-terminal hypervariable regions were highly extended and rich in glutamic
acid in polypeptides of Tnnt1 and Tnnt2, but not Tnnt3b. The Tnnt2 and Tnnt3b contain introns, whereas Tnnt1 is
intron-free. During development, large to small, alternatively spliced variants were detected in Tnnt2, but not in Tnnt1
or Tnnt3. Whole-mount in situ hybridization showed zebrafish Tnnt1 and Tnnt2 are activated during early
somitogenesis (10 hr postfertilization, hpf) and cardiogenesis (14 hpf), respectively, but Tnnt3b is not activated until
middle somitogenesis (18 hpf). Tnnt2 and Tnnt3b expression was cardiac- and fast-muscle specific, but Tnnt1 was
expressed in both slow and fast muscles. We propose that three, distinct, muscle-type Tnnt evolved after the
divergence of fish and deuterostome invertebrates. In zebrafish, the developmental regulation of Tnnt during
somitogenesis and cardiogenesis is more restricted and simpler than in tetrapods. These new findings may provide
insight into the developmental regulation and molecular evolution of vertebrate Tnnt. Developmental Dynamics 227:
266–279, 2003. © 2003 Wiley-Liss, Inc.
Subjects
zebrafish
troponin T
expression pattern
alternative splicing
gene structure
molecular evolution
Publisher
臺北市:國立臺灣大學漁業科學研究所
Type
journal article
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