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胚胎性横纹肌肉瘤中下调表达基因HumCyr 61的分离与克隆

solation and cloning of humCyr 61, a downstream gene in embryonic rhabdomyosarcoma
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摘要 分离和克隆胚胎性横纹肌肉瘤中下调表达基因 HumCyr 61。方法:利用计算机辅 助的同源扩增策略,成功克隆一个长1887bpcDNA,并与DenBank核酸数据库比较。结果:该基因 与鼠生长因子诱导早期表达的 Cyr61基因同源度为82%,在蛋白质水平上的同源度高达 92%,其 中对高级结构有重大贡献的半胱氨酸和脯氨酸等氨基酸残基高度保守。查新结果还显示,它包括 在胚胎性横纹肌肉瘤细胞系RD中表达呈下调表达的cDNA片段(GenBank接受号Z50168)和前列 腺癌患者良性组织中表达的cDNA片段(GenBank接受号Y09859)。此外,该基因与鸡CEF-10基因 和人结缔组织生长因子(CTCF)基因都具有较高的同源度。结论:推测这个新基因很可能是人类的 Cyr61基因,故命名为 HumCyr 61(GenBank注册号 AF031385)。 Aim: To isolate and clone humCyr 61, a downstream gene in embryonic rhabdomyosarco- ma. Methods: With amplification strategy addicted by computer, a novel 1887bp cDNA was successfully cloned and compared with the sequences in GeneBank. Results: the homology between the gene and Gyr 61 (A gene could be induced to express by mouse growth factor) was 82% in DNA sequence, and 92% in protein sequence. among them, Cystein residue and Proline residue highly conserved. This gene was included in cDNA fragments of embryonic rhabdomyosarcoma cell line RD(CenBank Reception Number: Z50168) and benign tissue of prostatic cancer (GenBank Reception Number: Y09859). In addition, there was homology between the gene and chicke CEF - 10 gene or human connective tissue growth factor (CTGF) gene. Conclusion: It was speculated that it might be human Cyr 61 gene and named HumCyr 61 (GenBank Register Number: AF 031385).
作者 程滨 毕安定
出处 《暨南大学学报(自然科学与医学版)》 CAS CSCD 2000年第2期18-21,共4页 Journal of Jinan University(Natural Science & Medicine Edition)
关键词 胚胎性横纹肌肉瘤 人Cyr61基因 基因克隆 分离 rhabdomyosarcoma HumCyr 61 cDNA gene cloning
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参考文献5

  • 1LAU L F,NATHANS D.Identification of a set of genes expressed during the G0/G1 transition of cultured mouse cell[].EMBO Journal.1985
  • 2BRUNNER A,CHJNN J,NLEUBAUER M,et al.Identification of a Gene family regulated by transforming growthfactor- β[].DNA and Cell Biology.1991
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  • 4MARIA L K,FAN E M O,GEORGE P Y,et al.Gyr 61, a product of a growth factor-inducible immediate - earlygene, promotes cell proliferation, migration, and adhesion[].Molecular and Cellular Probes.1996
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