中国动物传染病学报
中國動物傳染病學報
중국동물전염병학보
CHINESE JOURNAL OF VETERINARY PARASITOLOGY
2014年
3期
53-60
,共8页
胡跃%孙英杰%王晓旭%仇旭升%宋翠萍%谭磊%胡桂学%丁铲
鬍躍%孫英傑%王曉旭%仇旭升%宋翠萍%譚磊%鬍桂學%丁鏟
호약%손영걸%왕효욱%구욱승%송취평%담뢰%호계학%정산
鹅维甲酸诱导基因-I%鸡胚成纤维细胞系DF-1%PiggyBac转座系统
鵝維甲痠誘導基因-I%鷄胚成纖維細胞繫DF-1%PiggyBac轉座繫統
아유갑산유도기인-I%계배성섬유세포계DF-1%PiggyBac전좌계통
Goose retinoic acid inducible gene-I(RIG-I)%chicken embryo fibroblast cell line DF-1%Piggy-Bac transposon system
维甲酸诱导基因-I(retinoic acid inducible gene-I,RIG-I)是最近几年发现的一种细胞内模式识别受体,能够特异性的识别并结合病毒RNA,进而发挥抗病毒效应。RIG-I在进化中相对保守,但已有报道和我们的前期研究显示:家禽中鸭和鹅体内均有RIG-I受体,但鸡却缺乏RIG-I受体。为了研究这种天然缺失对鸡是否有不利影响,本研究利用PiggyBac转座系统将鹅源RIG-I转染入鸡胚成纤维细胞系DF-1,两次亚克隆后获得单个克隆,以荧光、RT-PCR及Western blot进行鉴定,最终获得稳定表达鹅RIG-I的DF-1细胞系,为进一步研究鸡的先天性免疫机制和鹅RIG-I的功能打下基础。
維甲痠誘導基因-I(retinoic acid inducible gene-I,RIG-I)是最近幾年髮現的一種細胞內模式識彆受體,能夠特異性的識彆併結閤病毒RNA,進而髮揮抗病毒效應。RIG-I在進化中相對保守,但已有報道和我們的前期研究顯示:傢禽中鴨和鵝體內均有RIG-I受體,但鷄卻缺乏RIG-I受體。為瞭研究這種天然缺失對鷄是否有不利影響,本研究利用PiggyBac轉座繫統將鵝源RIG-I轉染入鷄胚成纖維細胞繫DF-1,兩次亞剋隆後穫得單箇剋隆,以熒光、RT-PCR及Western blot進行鑒定,最終穫得穩定錶達鵝RIG-I的DF-1細胞繫,為進一步研究鷄的先天性免疫機製和鵝RIG-I的功能打下基礎。
유갑산유도기인-I(retinoic acid inducible gene-I,RIG-I)시최근궤년발현적일충세포내모식식별수체,능구특이성적식별병결합병독RNA,진이발휘항병독효응。RIG-I재진화중상대보수,단이유보도화아문적전기연구현시:가금중압화아체내균유RIG-I수체,단계각결핍RIG-I수체。위료연구저충천연결실대계시부유불리영향,본연구이용PiggyBac전좌계통장아원RIG-I전염입계배성섬유세포계DF-1,량차아극륭후획득단개극륭,이형광、RT-PCR급Western blot진행감정,최종획득은정표체아RIG-I적DF-1세포계,위진일보연구계적선천성면역궤제화아RIG-I적공능타하기출。
Retinoic acid inducible gene-I (RIG-I) is a family member of cytoplasmic pattern recognition receptors (PRRs), which acts as a sensor for RNA virus and plays an important role in antiviral innate immunity. RIG-I is evolutionally conserved among most species. However, several reports and our previous studies have identified that receptors for RIG-I exist in both ducks and geese, but not in chickens. To investigate whether this natural loss of RIG-I plays a negative role in chicken, goose RIG-I was transfected into chicken embryo fibroblast cell line DF-1 through PiggyBac transposon system. Monoclonal cells were obtained from twice sub-cloned cultures. DF-1 cells stably expressing goose RIG-I were identified by detection of fluorescence, RT-PCR and Western blot. The present study has laid the foundation for future research on mechanism of chicken innate immunity and function of goose RIG-I.