用户名: 密码: 验证码:
Genomic organization, promoter activity of grass carp MDA5 and the association of its polymorphisms with susceptibility/resistance to grass carp reovirus
详细信息查看全文 | 推荐本文 |
摘要
MDA5 (melanoma-differentiation-associated gene 5), a member of the RLR (retinoic acid-inducible gene I-like receptor) family, plays a pivotal role in innate immunity against viral infection. In the present study, the organization of grass carp (Ctenopharyngodon idella) MDA5 (CiMDA5) gene sequence was elucidated and promoter activity of its 5鈥?flanking region was detected. In addition, single nucleotide polymorphisms (SNPs) were investigated to explore their association with susceptibility/resistance to grass carp reovirus (GCRV). The CiMDA5 genomic sequence is composed of 10,906 bp, containing seven exons and six introns, which is distinct from its counterparts with numbers of exons. The 5鈥?flanking region of CiMDA5 gene, containing several putative transcription factor binding sites, was amplified using genome walking technique, exhibiting promoter activity. Six SNPs were discovered in the complete sequence of CiMDA5. Five of them locate in introns and one in 5鈥?flanking region. The genotype and allele distribution were examined by PCR-RFLP in susceptible and resistant fish. The results indicate that genotypes at the 鈭?13 C/G and 3338 A/C loci were significantly associated with the resistance to GCRV (P < 0.05). Furthermore, at 鈭?13 C/G site, no CC genotype individual was found; the mortality in GG genotype group was 42.65%, which was significantly lower than that in CG genotype group (73.91%) (P < 0.05). The mortality in CC (33.33%) genotype at 3338 A/C locus was significantly lower than that in AA and AC genotype (61.54%, 45.95%respectively) (P < 0.05). The data demonstrate that 鈭?13 G and 3338 C carrier are resistant to GCRV. These results provide potential markers for further investigation of selective breeding of resistant grass carp to GCRV.

© 2004-2018 中国地质图书馆版权所有 京ICP备05064691号 京公网安备11010802017129号

地址:北京市海淀区学院路29号 邮编:100083

电话:办公室:(+86 10)66554848;文献借阅、咨询服务、科技查新:66554700