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svp基因在果蝇副心肌细胞生长中的作用(英文) 被引量:1

Role of svp in Drosophila Pericardial Cell Growth
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摘要 果蝇心脏位于身体背部,是一个体节性重复的线性管状结构。在hedgehog(hh)基因的信号诱导下,seven-up(svp) 基因调控果蝇的心脏发育,在每个体节的两个心肌细胞和两个副心肌细胞中表达。结果表明,在svp纯合突变体中,报告 基因lacZ存心肌细胞中的表达图式正常,但在副心肌细胞中的表达图型明显异常,而且部分EPC细胞生长尺寸增加。某 些体节的DA1肌肉祖细胞缺失,晚期突变体胚胎体壁肌肉细胞也呈现异常,表明基因svp的活性对果蝇副心肌细胞、DA1 肌肉祖细胞和体壁肌肉细胞的分化是必须的,并且可能与EPC副心肌细胞的尺寸生长有关。 The Drosophila dorsal vessel is a segmentally repeated linear organ, in which seven-up (svp) is expressed in two pairs of cardioblasts and two pairs of pericardial cells in each segment. Under the control of hedgehog (hh) signaling from the dorsal ectoderm, svp participates in diversifying cardioblast identities within each segment. In this experiment, the homozygous embryos of svp mutants exhibited an increase in cell size of Eve positive pericardial cells (EPCs) and a disarranged expression pattern, while the cardioblasts pattern of svp-lacZ expression was normal. In the meantime, the DA1 muscle founders were absent in some segments in svp mutant embryos, and the dorsal somatic muscle patterning was also severely damaged in the late stage mutant embryos, suggesting that svp is required for the differentiation of Eve-positive pericardial cells and DA1 muscle founders and may have a role in EPC cell growth.
出处 《Acta Genetica Sinica》 SCIE CAS CSCD 北大核心 2006年第1期32-40,共9页
基金 This Work Was Supported by the National Natural Sciences Foundation of China (No.30270644, 3021010392)the Natural Sciences Foundation of Huan Province of China (No.02JJY4026)the Foundation of the Department of Education in Hunan Province of China(No.02B017).
关键词 seven-up(svp)基因 副心肌细胞 EPC(Eve正染色的副心肌细胞) DA1 细胞生长 seven-up (svp) pericardial cells EPCs DA1 cell growth
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  • 1Rizki T M, Rizki R M. Larval adipose tissue of homeotic bithorax mutants of Drosophila. Dev Biol,1978, 65(2): 476-482.
  • 2Hah Z, Fujioka M, Su M, Liu M, Jaynes J B, Bodmer R.Transcriptional integration of competence modulated by mutual repression generates cell-type specificity within the cardiogenic mesoderm. Developmental Biology,2002, 252: 225-240.
  • 3Cripps R M, Olson E N. Control of cardiac development by an evolutionarily conserved transcriptional network.Dev Biol, 2002, 246(1): 14-28.
  • 4Lai K H, Chang F Y, Tsay S H, Lu L C, Cheng J T, Jeng S S, Wu T C, Ng W W, Jeng J S, Lee S. Medical treatment of duodenal ulcer: acid inhibition or Helicobacter pylori eradication? Gastroenterol Hepatol, 1991, 6(2): 141-144.
  • 5Bodmer R, Frasch M. Genetic determination of Drosophila heart development. In: Heart development. London:Academic Press, 1999, 65-90.
  • 6Gajewski K, Choi C Y, Kim Y, Schulz R A. Genetically distinct cardial cells within the Drosophila heart. Genesis,2000, 28(1): 36-43.
  • 7Lo P C, Skeath J B, Gajewski K, Schulz R A, Frasch M.Homeotic genes autonomously specify the anteroposterior subdivision of the Drosophila dorsal vessel into aorta and heart. Developmental Biology, 2002, 251: 307-319.
  • 8Molina M R, Cripps R M. Ostia, the inflow tracts of the Drosophila heart, develop from a genetically distinct subset of cardial cells. Mech Dev, 2001, 109(1): 51-59.
  • 9Ward E J, Skeath, J B. Characterization of a novel subset of cardiac cells and their progenitors in the Drosophila embryo. Development, 2000, 127: 4959-4969.
  • 10Lo P C, Frasch M. A role for the COUP-related gene seven-up in the diversification of cardioblast identities in the dorsal vessel of Drosophila. Mechanisms of Development, 2001, 104: 49-60.

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