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Nramp-1基因在Bcgr和Bcgs小鼠中的序列分析及表达

Sequence analysis and expression of Nramp-1 gene in Bcgr and Bcgs mice.

作者信息

Nakanaga K, Maeda S, Myojin Y, Xu D L, Goto Y

机构信息

Department of Bioregulation, National Institute of Infectious Diseases, Tokyo, Japan.

出版信息

J Vet Med Sci. 1999 Jun;61(6):717-20. doi: 10.1292/jvms.61.717.

Abstract

Nucleic acid sequence of complemental DNA open reading frame for Nramp-1 gene was compared among DBA/2 (Bcgr), C57BL/6 (Bcgs) and C57BL/6-Bcgr mice which was previously developed as M. avium-resistant mouse strain (Xu, et al. Veterinary Microbiology 50:73-79 (1996). Total RNA was isolated from various organs of DBA/2, C57BL/6 and C57BL/6-Bcgr. Nramp-1 cDNA was constructed from their mRNAs by gene amplification (PCR) technique and their open reading frame sequences were compared. The results clearly showed that our C57BL/6-Bcgr was almost identical with the DNA sequence of the DBA/2 mice. In contrast, C57BL/6-Bcgs mice differed only on the substitution of adenine for guanine of the nucleic acid at position 596. This corresponded to the site of amino acid substitution (glycine to asparate) at position 169 in predicted NRAMP which had been reported. The expression of Nramp-1 mRNA was more prominent in spleens and livers and there appeared to be no significant difference among the strains of mice.

摘要

在DBA/2(Bcgr)、C57BL/6(Bcgs)和C57BL/6 - Bcgr小鼠(先前被培育为抗鸟分枝杆菌小鼠品系,Xu等人,《兽医微生物学》50:73 - 79 (1996))之间比较了Nramp - 1基因互补DNA开放阅读框的核酸序列。从DBA/2、C57BL/6和C57BL/6 - Bcgr的各种器官中分离总RNA。通过基因扩增(PCR)技术从它们的mRNA构建Nramp - 1 cDNA,并比较它们的开放阅读框序列。结果清楚地表明,我们的C57BL/6 - Bcgr与DBA/2小鼠的DNA序列几乎相同。相比之下,C57BL/6 - Bcgs小鼠仅在核酸第596位的鸟嘌呤被腺嘌呤取代。这与已报道的预测NRAMP中第169位氨基酸取代位点(甘氨酸变为天冬氨酸)相对应。Nramp - 1 mRNA的表达在脾脏和肝脏中更为突出,并且在小鼠品系之间似乎没有显著差异。

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