中国水产科学
中國水產科學
중국수산과학
Journal of Fishery Sciences of China
2014年
6期
1134-1145
,共12页
黎建平%高风英%卢迈新%曹建萌%朱华平%可小丽%刘志刚
黎建平%高風英%盧邁新%曹建萌%硃華平%可小麗%劉誌剛
려건평%고풍영%로매신%조건맹%주화평%가소려%류지강
尼罗罗非鱼%MHC?α%多态性分析%组织表达
尼囉囉非魚%MHC?α%多態性分析%組織錶達
니라라비어%MHC?α%다태성분석%조직표체
Nile tilapia%major histocompatibility complex class ?α (MHC ?α)%molecular polymorphism%tissue expression
通过同源克隆和末端快速扩增(RACE)方法,获得尼罗罗非鱼(Oreochromis niloticus)的MHC ?α全长cDNA,分析其多态性和组织表达特征。获得的尼罗罗非鱼MHC?αcDNA全长为1533 bp,其ORF为1053 bp。编码的蛋白质分子包含信号肽、MHC结构域、IGc1结构域和跨膜区,并存在丰富的磷酸化位点。与其他硬骨鱼类和哺乳类的相似性在26.86%~74.0%。从6尾鱼中共分离得到6条不同的MHC ?α cDNA序列,其序列中存在多个单核苷酸多态性位点,说明MHC?αcDNA存在丰富的多态性。qPCR检测表明, MHC?α基因在脾和心中表达量较高,中等程度表达于鳃、肠和肾中,在脑、肝、胃、皮肤和肌肉中表达量较低。对尼罗罗非鱼进行人工感染无乳链球菌(Streptococcus agalactiae)后, MHC?α基因的mRNA表达水平在鳃、肾、心脏和脾4个组织中均发生了不同程度的变化。结果表明MHC Iα基因参与罗非鱼免疫反应,在免疫应答中发挥重要功能。本研究通过研究尼罗罗非鱼MHC?α的生物学活性、功能和表达调控,旨在为揭示尼罗罗非鱼免疫抗感染机制提供基础资料,并为利用MHC?α作为候选基因筛选尼罗罗非鱼抗病相关分子标记、辅助抗病品系的选育奠定基础。
通過同源剋隆和末耑快速擴增(RACE)方法,穫得尼囉囉非魚(Oreochromis niloticus)的MHC ?α全長cDNA,分析其多態性和組織錶達特徵。穫得的尼囉囉非魚MHC?αcDNA全長為1533 bp,其ORF為1053 bp。編碼的蛋白質分子包含信號肽、MHC結構域、IGc1結構域和跨膜區,併存在豐富的燐痠化位點。與其他硬骨魚類和哺乳類的相似性在26.86%~74.0%。從6尾魚中共分離得到6條不同的MHC ?α cDNA序列,其序列中存在多箇單覈苷痠多態性位點,說明MHC?αcDNA存在豐富的多態性。qPCR檢測錶明, MHC?α基因在脾和心中錶達量較高,中等程度錶達于鰓、腸和腎中,在腦、肝、胃、皮膚和肌肉中錶達量較低。對尼囉囉非魚進行人工感染無乳鏈毬菌(Streptococcus agalactiae)後, MHC?α基因的mRNA錶達水平在鰓、腎、心髒和脾4箇組織中均髮生瞭不同程度的變化。結果錶明MHC Iα基因參與囉非魚免疫反應,在免疫應答中髮揮重要功能。本研究通過研究尼囉囉非魚MHC?α的生物學活性、功能和錶達調控,旨在為揭示尼囉囉非魚免疫抗感染機製提供基礎資料,併為利用MHC?α作為候選基因篩選尼囉囉非魚抗病相關分子標記、輔助抗病品繫的選育奠定基礎。
통과동원극륭화말단쾌속확증(RACE)방법,획득니라라비어(Oreochromis niloticus)적MHC ?α전장cDNA,분석기다태성화조직표체특정。획득적니라라비어MHC?αcDNA전장위1533 bp,기ORF위1053 bp。편마적단백질분자포함신호태、MHC결구역、IGc1결구역화과막구,병존재봉부적린산화위점。여기타경골어류화포유류적상사성재26.86%~74.0%。종6미어중공분리득도6조불동적MHC ?α cDNA서렬,기서렬중존재다개단핵감산다태성위점,설명MHC?αcDNA존재봉부적다태성。qPCR검측표명, MHC?α기인재비화심중표체량교고,중등정도표체우새、장화신중,재뇌、간、위、피부화기육중표체량교저。대니라라비어진행인공감염무유련구균(Streptococcus agalactiae)후, MHC?α기인적mRNA표체수평재새、신、심장화비4개조직중균발생료불동정도적변화。결과표명MHC Iα기인삼여라비어면역반응,재면역응답중발휘중요공능。본연구통과연구니라라비어MHC?α적생물학활성、공능화표체조공,지재위게시니라라비어면역항감염궤제제공기출자료,병위이용MHC?α작위후선기인사선니라라비어항병상관분자표기、보조항병품계적선육전정기출。
Major histocompatibility complex is a genetic region of the chromosome. It consists of a series of closely linked highly polymorphic loci that stimulate the body’s immune response by encoding a class of cell sur-face transmembrane protein that binds to T lymphocytes and presents endogenous and exogenous antigens to it. Based on the techniques of homology cloning and RACE-PCR, full-length cDNA of MHC ?α was cloned from Nile tilapia. In addition, cDNA polymorphism and mRNA expression were also analyzed. The total length of MHC1α cDNA was 1 553 bp, which the ORF (open reading frame) was 1 053 bp in length. Sequence analysis showed that the deduced protein sequence of MHC?αincluded a leader peptide , a MHC-I domain, an IGc1domain, and a transmembrane region. The putative protein had 26.86%–74.0% identity with those of other teleosts and mammals. Six different MHC?αcDNA sequences were obtained from six individuals. There were multiple single nucleotide polymorphisms among the six MHC?αcDNA sequences. This indicates that MHCα?cDNA has abu n-dant polymorphism. qPCR detected the highest expression level of MHCα?in spleen and heart , moderate expres-sion in gill, kidney and intestine, and the lowest expression in brain, liver, stomach, skin and muscle. Different changes were found in the expressions of MHαC ?mRNA in the gill , kidney, heart and spleen after being chal-lenged with Streptococcus agalactiae. The findings provide useful information for further investigation to select a disease resistant molecular marker of Nile tilapia using MHC Iαas a candidate gene.