淡水渔业
淡水漁業
담수어업
FRESHWATER FISHERIES
2014年
1期
14-19
,共6页
叶华%朱成科%郑宗林%吴青%郑曙明
葉華%硃成科%鄭宗林%吳青%鄭曙明
협화%주성과%정종림%오청%정서명
齐口裂腹鱼(Schizothorax prenanti)%Toll 样受体%髓样分化因子88(MyD88)
齊口裂腹魚(Schizothorax prenanti)%Toll 樣受體%髓樣分化因子88(MyD88)
제구렬복어(Schizothorax prenanti)%Toll 양수체%수양분화인자88(MyD88)
Schizothorax prenanti%Toll-like receptor%myeloid differentiation factor 88 (MyD88)
利用RT-PCR和RACE-PCR技术获得了齐口裂腹鱼( Schizothorax prenanti) TLR信号转导途径中的关键接头分子MyD88基因cDNA全长序列,该序列共1479 bp,包括编码284个氨基酸残基的855 bp的开放阅读框,177 bp 5′非翻译区和447 bp 3′非翻译区,编码284个氨基酸。利用SMART软件分析,结果显示,该蛋白在N端和C端分别存在死亡结构域(Death domain, DD)和TIR结构域(Toll/IL-1 receptor homology domain, TIR)。齐口裂腹鱼MyD88氨基酸序列与鲤( Cyprinus carpio)、斑马鱼( Danio rerio)、大黄鱼( Larimichthys crocea)、花鲈( Lateolabrax japonicas)、虹鳟( Oncorhynchus mykiss)的相似性为69.37%~91.90%,其中与斑马鱼的相似性最高。用 NJ 法构建的系统进化树中,齐口裂腹鱼MyD88和其它鱼类MyD88聚为一枝。
利用RT-PCR和RACE-PCR技術穫得瞭齊口裂腹魚( Schizothorax prenanti) TLR信號轉導途徑中的關鍵接頭分子MyD88基因cDNA全長序列,該序列共1479 bp,包括編碼284箇氨基痠殘基的855 bp的開放閱讀框,177 bp 5′非翻譯區和447 bp 3′非翻譯區,編碼284箇氨基痠。利用SMART軟件分析,結果顯示,該蛋白在N耑和C耑分彆存在死亡結構域(Death domain, DD)和TIR結構域(Toll/IL-1 receptor homology domain, TIR)。齊口裂腹魚MyD88氨基痠序列與鯉( Cyprinus carpio)、斑馬魚( Danio rerio)、大黃魚( Larimichthys crocea)、花鱸( Lateolabrax japonicas)、虹鱒( Oncorhynchus mykiss)的相似性為69.37%~91.90%,其中與斑馬魚的相似性最高。用 NJ 法構建的繫統進化樹中,齊口裂腹魚MyD88和其它魚類MyD88聚為一枝。
이용RT-PCR화RACE-PCR기술획득료제구렬복어( Schizothorax prenanti) TLR신호전도도경중적관건접두분자MyD88기인cDNA전장서렬,해서렬공1479 bp,포괄편마284개안기산잔기적855 bp적개방열독광,177 bp 5′비번역구화447 bp 3′비번역구,편마284개안기산。이용SMART연건분석,결과현시,해단백재N단화C단분별존재사망결구역(Death domain, DD)화TIR결구역(Toll/IL-1 receptor homology domain, TIR)。제구렬복어MyD88안기산서렬여리( Cyprinus carpio)、반마어( Danio rerio)、대황어( Larimichthys crocea)、화로( Lateolabrax japonicas)、홍준( Oncorhynchus mykiss)적상사성위69.37%~91.90%,기중여반마어적상사성최고。용 NJ 법구건적계통진화수중,제구렬복어MyD88화기타어류MyD88취위일지。
Prenant′s schizothoracin , Schizothorax prenanti ( Tchang ) , is one of the most important cold fish species in China, and it's an important commercial fish distributed through upper reaches of the Yangtze River .The full-length cDNA of myeloid differentiation factor 88 ( MyD88 ) isolated by RT-PCR and RACE-PCR methods was 1479 bp, including an open reading frame ( ORF) of 855 bp encoding 284 amino acid residues , a 5′-terminal untranslated region ( UTR) of 177 bp, a 3′-terminal UTR of 447 bp.The MyD88 protein comprised a death domain on N terminal and a TIR domain on C terminal analysed by SMART program .The MyD88 amino acid sequence of S.prenanti had 69.37%~91.90% identity with Cyprinus carpio, Danio rerio, Larimichthys crocea, Lateolabrax japonicas, Oncorhynchus mykiss, and had the high-est similarity with D.rerio.Phylogenetic tree was constructed by neighbor-joining method which revealed that MyD 88 of S.prenanti was clustered with MyD 88 from other teleost fish reported previously .