中国水产科学
中國水產科學
중국수산과학
Journal of Fishery Sciences of China
2015年
5期
896-907
,共12页
李伟杰%傅明骏%赵超%郭松%江世贵%周发林%杨其彬%邱丽华
李偉傑%傅明駿%趙超%郭鬆%江世貴%週髮林%楊其彬%邱麗華
리위걸%부명준%조초%곽송%강세귀%주발림%양기빈%구려화
斑节对虾%cyclin Y基因%分子克隆%实时荧光定量PCR%原核表达
斑節對蝦%cyclin Y基因%分子剋隆%實時熒光定量PCR%原覈錶達
반절대하%cyclin Y기인%분자극륭%실시형광정량PCR%원핵표체
Penaeus monodon%cyclin Y gene%molecular cloning%real-time PCR%prokaryotic expression Corresponding author:QIU Lihua. E-mail:qiu902126.com
为了研究细胞周期蛋白Y(cyclin Y)在斑节对虾(Penaeus monodon)卵巢发育中的作用,从斑节对虾转录组数据中筛选获得cyclin Y基因部分序列,采用SMART-RACE方法克隆得到斑节对虾细胞周期蛋白Y (Pm-cyclin Y)基因cDNA全序列。Pm-cyclin Y基因cDNA全长1576 bp,其中包含108 bp的5′非编码区(5′UTR)和439 bp的3′非编码区(3′UTR)以及1029 bp的开放阅读框(ORF),可编码342个氨基酸。生物信息学分析显示,其编码的氨基酸序列有1个保守的周期蛋白框(cyclin box)同源结构域(172~257 aa),预测的分子量约为37.6 kD,理论等电点6.64。实时定量 PCR 显示其 mRNA 在卵巢的表达量显著高于其他组织(P<0.05);并且在卵巢5个不同发育期都有表达,在III期卵巢中的表达量最高。本研究通过原核表达方法对Pm-cyclin Y进行重组表达,为其蛋白质功能方面的研究奠定了基础。
為瞭研究細胞週期蛋白Y(cyclin Y)在斑節對蝦(Penaeus monodon)卵巢髮育中的作用,從斑節對蝦轉錄組數據中篩選穫得cyclin Y基因部分序列,採用SMART-RACE方法剋隆得到斑節對蝦細胞週期蛋白Y (Pm-cyclin Y)基因cDNA全序列。Pm-cyclin Y基因cDNA全長1576 bp,其中包含108 bp的5′非編碼區(5′UTR)和439 bp的3′非編碼區(3′UTR)以及1029 bp的開放閱讀框(ORF),可編碼342箇氨基痠。生物信息學分析顯示,其編碼的氨基痠序列有1箇保守的週期蛋白框(cyclin box)同源結構域(172~257 aa),預測的分子量約為37.6 kD,理論等電點6.64。實時定量 PCR 顯示其 mRNA 在卵巢的錶達量顯著高于其他組織(P<0.05);併且在卵巢5箇不同髮育期都有錶達,在III期卵巢中的錶達量最高。本研究通過原覈錶達方法對Pm-cyclin Y進行重組錶達,為其蛋白質功能方麵的研究奠定瞭基礎。
위료연구세포주기단백Y(cyclin Y)재반절대하(Penaeus monodon)란소발육중적작용,종반절대하전록조수거중사선획득cyclin Y기인부분서렬,채용SMART-RACE방법극륭득도반절대하세포주기단백Y (Pm-cyclin Y)기인cDNA전서렬。Pm-cyclin Y기인cDNA전장1576 bp,기중포함108 bp적5′비편마구(5′UTR)화439 bp적3′비편마구(3′UTR)이급1029 bp적개방열독광(ORF),가편마342개안기산。생물신식학분석현시,기편마적안기산서렬유1개보수적주기단백광(cyclin box)동원결구역(172~257 aa),예측적분자량약위37.6 kD,이론등전점6.64。실시정량 PCR 현시기 mRNA 재란소적표체량현저고우기타조직(P<0.05);병차재란소5개불동발육기도유표체,재III기란소중적표체량최고。본연구통과원핵표체방법대Pm-cyclin Y진행중조표체,위기단백질공능방면적연구전정료기출。
Cyclin Y is a newly discovered cell cycle-related protein that plays an important role during embryonic de-velopment, cell cycle progression and development, and disease. Current research on cyclin Y is very active but no data have been reported on cyclin Y in crustaceans. Gonads of the black tiger shrimp, Penaeus monodon, mature if the eye stalk is removed. Thus, the full-length cyclin Y cDNA sequence from P. monodon (denoted as Pm-cyclin Y) was ob-tained using the rapid amplification of complementary DNA ends method to better understand the potential function of cyclin Y in the regulation of shrimp reproduction. The full-length cDNA sequence was 1578 bp and contained 108 bp 5′untranslated region (UTR) and a 439 bp 3′UTR. The open reading frame was 1029 bp and coded 342 amino acids (aa). A bioinformatics analysis showed that the amino acid coding sequence had a conserved cyclin box and the ho-mologous protein box structure domain was 172–257 aa. The predicted molecular weight was about 38.7 kD, and the theoretical isoelectric point was 6.64. A real-time quantitative polymerase chain reaction analysis detected significantly higher Pm-cyclin Y mRNA expression in the ovary than that in other tissues. Pm-cyclin Y mRNA was expressed in the ovary at five different developmental stages, and the expression level was highest during phase III. The study abtained recombinant expression Pm-cyclin Y in prokaryotes and offered theoretical basis for further research on Pm-cyclin pro-tein function. These results provide a basis for further functional studies of Pm-cyclin Y.