海洋科学
海洋科學
해양과학
MARINE SCIENCES
2014年
4期
7-14
,共8页
张若云%徐广锐%潘聪%谢莉萍%王洪钟%张贵友%张荣庆
張若雲%徐廣銳%潘聰%謝莉萍%王洪鐘%張貴友%張榮慶
장약운%서엄예%반총%사리평%왕홍종%장귀우%장영경
诱导多功能干细胞%转录因子%克隆%合浦珠母贝(Pinctada fucata)
誘導多功能榦細胞%轉錄因子%剋隆%閤浦珠母貝(Pinctada fucata)
유도다공능간세포%전록인자%극륭%합포주모패(Pinctada fucata)
ips cells%transcription factors%cloning%Pinctada fucata
转录因子Sox2、Oct4、c-Myc和KLF4在iPS细胞研究中具有重要作用,将它们加入体外培养的细胞中,可以诱导体细胞去分化成为多能干细胞。作者通过 RACE-PCR 技术从合浦珠母贝(Pinctada fucata)的外套膜组织中克隆获得了3个转录因子--c-Myc、Sox2及KLF4的cDNA。c-Myc全长1585bp,开放阅读框的长度为1131bp,编码376个氨基酸,蛋白结构分析表明它具有保守的 HLH和 Myc-N结构域。Sox2全长1908bp,开放阅读框长度为990bp,编码329个氨基酸,蛋白结构分析它具有保守的HMG-box和Soxp结构域。KLF4全长2268bp,开放阅读框长624bp,编码207个氨基酸,预测该蛋白具有两个zf-H2C2_2结构域。BLAST分析它们均与太平洋牡蛎的相关蛋白具有较高同源性,说明其与太平洋牡蛎亲缘关系更近。RT-P C R实验发现这3个基因在合浦珠母贝外套膜、足、生殖腺、内脏团、闭壳肌和鳃6种组织中均有表达,表明它们是非常保守的转录因子。本研究对于合浦珠母贝细胞系建立和研究具有启发意义。
轉錄因子Sox2、Oct4、c-Myc和KLF4在iPS細胞研究中具有重要作用,將它們加入體外培養的細胞中,可以誘導體細胞去分化成為多能榦細胞。作者通過 RACE-PCR 技術從閤浦珠母貝(Pinctada fucata)的外套膜組織中剋隆穫得瞭3箇轉錄因子--c-Myc、Sox2及KLF4的cDNA。c-Myc全長1585bp,開放閱讀框的長度為1131bp,編碼376箇氨基痠,蛋白結構分析錶明它具有保守的 HLH和 Myc-N結構域。Sox2全長1908bp,開放閱讀框長度為990bp,編碼329箇氨基痠,蛋白結構分析它具有保守的HMG-box和Soxp結構域。KLF4全長2268bp,開放閱讀框長624bp,編碼207箇氨基痠,預測該蛋白具有兩箇zf-H2C2_2結構域。BLAST分析它們均與太平洋牡蠣的相關蛋白具有較高同源性,說明其與太平洋牡蠣親緣關繫更近。RT-P C R實驗髮現這3箇基因在閤浦珠母貝外套膜、足、生殖腺、內髒糰、閉殼肌和鰓6種組織中均有錶達,錶明它們是非常保守的轉錄因子。本研究對于閤浦珠母貝細胞繫建立和研究具有啟髮意義。
전록인자Sox2、Oct4、c-Myc화KLF4재iPS세포연구중구유중요작용,장타문가입체외배양적세포중,가이유도체세포거분화성위다능간세포。작자통과 RACE-PCR 기술종합포주모패(Pinctada fucata)적외투막조직중극륭획득료3개전록인자--c-Myc、Sox2급KLF4적cDNA。c-Myc전장1585bp,개방열독광적장도위1131bp,편마376개안기산,단백결구분석표명타구유보수적 HLH화 Myc-N결구역。Sox2전장1908bp,개방열독광장도위990bp,편마329개안기산,단백결구분석타구유보수적HMG-box화Soxp결구역。KLF4전장2268bp,개방열독광장624bp,편마207개안기산,예측해단백구유량개zf-H2C2_2결구역。BLAST분석타문균여태평양모려적상관단백구유교고동원성,설명기여태평양모려친연관계경근。RT-P C R실험발현저3개기인재합포주모패외투막、족、생식선、내장단、폐각기화새6충조직중균유표체,표명타문시비상보수적전록인자。본연구대우합포주모패세포계건립화연구구유계발의의。
The four transcription factors named Sox2, Oct4, c-Myc and KLF4 can reprogram differentiated in vitro culture cells to an embryonic-like state, in another name, ips cells. The complete gene sequence of c-Myc, Sox2 and KLF4 from Pinctada fucata was amplified by RACE PCR. The complete sequence of c-Myc gene was 1585 bp and the complete ORF length was 1131 bp which encoded a protein with 376 amino acid residues. The analysis of pro-tein structure showed c-Myc protein had the conservative HLH and Myc-N domains, which have the DNA-binding function. Sox2 gene has the complete sequence of 1908 bp and the complete ORF length of 990 bp which encoded a protein with 329 amino acid residues. And the Sox2 protein had the conservative HMG-box and Soxp domains, which have the DNA-regulation function. KLF4 gene was 2268 bp long and the complete ORF length was 624 bp which encoded a protein with 207 amino acid residues. And the KLF4 protein had two zf-H2C2_2 domains, which have the DNA-binding function. Blast analysis indicated the three deduced amino acid sequences of the c-Myc, Sox2 and KLF4 genes from P. fucata showed high homology with proteins from Crassostrea gigas. RT-PCR result shows that these three genes were expressed in all six tissues from P. fucata including mantle, foot, gonal, visceral mass, adductor muscle and gill, suggesting that these genes were conservative transcriptional factors. Our study inspires the work on cell culture and research in P. fucata.