渔业科学进展
漁業科學進展
어업과학진전
MARINE FISHERIES RESEARCH
2014年
5期
70-75
,共6页
姜薇%姚琳%江艳华%李风铃%牟海津%刘慧%翟毓秀
薑薇%姚琳%江豔華%李風鈴%牟海津%劉慧%翟毓秀
강미%요림%강염화%리풍령%모해진%류혜%적육수
太平洋牡蛎%类FUT2基因%克隆%组织表达
太平洋牡蠣%類FUT2基因%剋隆%組織錶達
태평양모려%류FUT2기인%극륭%조직표체
Crassostrea gigas%FUT2-like gene%Clone%mRNA expression
通过同源克隆的方法获得太平洋牡蛎(Crassostrea gigas)类FUT2基因的cDNA序列,分析其在牡蛎中的组织表达差异。研究结果表明,太平洋牡蛎类FUT2基因cDNA全长为1941 bp,包含180 bp的5¢非翻译区、1086 bp的编码361个氨基酸的开放阅读框及675 bp的3¢非翻译区。分子进化聚类分析结果显示,太平洋牡蛎类FUT2基因与家鼠(Mus musculus)等哺乳动物的FUT2基因聚为1个分支。此外,类FUT2基因mRNA在太平洋牡蛎成贝的肝胰脏、闭壳肌、外套膜、唇瓣、鳃等5个组织中均有分布,其中在唇瓣中的表达量最低,在其余4个组织中的表达量差异不显著。本研究表明,牡蛎中类A型组织血型抗原HBGA很可能存在与人A型HBGA相似的合成途径,可为进一步探索牡蛎特异性富集诺如病毒NoV的分子机制奠定研究基础。
通過同源剋隆的方法穫得太平洋牡蠣(Crassostrea gigas)類FUT2基因的cDNA序列,分析其在牡蠣中的組織錶達差異。研究結果錶明,太平洋牡蠣類FUT2基因cDNA全長為1941 bp,包含180 bp的5¢非翻譯區、1086 bp的編碼361箇氨基痠的開放閱讀框及675 bp的3¢非翻譯區。分子進化聚類分析結果顯示,太平洋牡蠣類FUT2基因與傢鼠(Mus musculus)等哺乳動物的FUT2基因聚為1箇分支。此外,類FUT2基因mRNA在太平洋牡蠣成貝的肝胰髒、閉殼肌、外套膜、脣瓣、鰓等5箇組織中均有分佈,其中在脣瓣中的錶達量最低,在其餘4箇組織中的錶達量差異不顯著。本研究錶明,牡蠣中類A型組織血型抗原HBGA很可能存在與人A型HBGA相似的閤成途徑,可為進一步探索牡蠣特異性富集諾如病毒NoV的分子機製奠定研究基礎。
통과동원극륭적방법획득태평양모려(Crassostrea gigas)류FUT2기인적cDNA서렬,분석기재모려중적조직표체차이。연구결과표명,태평양모려류FUT2기인cDNA전장위1941 bp,포함180 bp적5¢비번역구、1086 bp적편마361개안기산적개방열독광급675 bp적3¢비번역구。분자진화취류분석결과현시,태평양모려류FUT2기인여가서(Mus musculus)등포유동물적FUT2기인취위1개분지。차외,류FUT2기인mRNA재태평양모려성패적간이장、폐각기、외투막、진판、새등5개조직중균유분포,기중재진판중적표체량최저,재기여4개조직중적표체량차이불현저。본연구표명,모려중류A형조직혈형항원HBGA흔가능존재여인A형HBGA상사적합성도경,가위진일보탐색모려특이성부집낙여병독NoV적분자궤제전정연구기출。
Norovirus (NoV) is the most common pathogen of acute viral gastroenteritis worldwide, which causes serious issues on public health and food safety. Histo-blood group antigens (HBGAs) have been recognized as receptors of NoV. It has been reported that type A-like HBGA presents in oyster gastrointestinal cells and induces specific accumulation of NoV in oysters. Alpha-1,2-fucosyltransferase (FUT2) is one of the key enzymes required in the HBGA synthesis. However, studies on FUT2 in oysters and other aquatic animals have been lacking. In this study, we cloned the FUT2-like gene in oysters (Crassostrea gigas) using homologous gene sequence method, and also analyzed the expression of FUT2-like gene in five tissues, including hepatopancrea, adductor muscle, mantle, labial palp and gills. The FUT2-like cDNA has a full length of 1941 bp, including a180-bp 5¢-untranslated region (UTR), a 1086-bp open reading frame (ORF) that encodes a protein of 361 amino acids, and a 675-bp 3¢-untranslated region (UTR). The molecular evolution analysis showed that the FUT2-like gene in oyster should be categorized into the same branch as FUT2 genes in Mus musculus and other mammals. The expression pattern of FUT2-like gene was analyzed in 5 tissues mentioned above. The results showed that the mRNAs of this gene were expressed in all 5 tissues; the expression level in labial palp was significantly lower than that in the other 4 tissues. Our results indicated that A-like HBGA in oyster might have a similar biosynthesis pathway as Type A HBGA in human. Our study should provide insights into the molecular mechanism of the accumulation of NoV in oysters.