Genetic control of the spontaneous hypertension in the NZB/Cr strain of mice. Immunogenetic considerations.

U G Svendsen, C M Koch, B Rubin
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Abstract

NZB/Cr mice spontaneously develop a high blood pressure. This hypertension is developed during the first two months of age. F1-hybrids between NZB/Cr and C57/B1/6J (a normotensive mouse strain which does not spontaneously develop hypertension) also develop a high blood pressure, showing that the phenomenon is inherited as a dominant trait. The gene(s) responsive for the phenotypic high blood pressure is localised outside the MHC of the mouse (the H-2 complex). However, H-2 typing of backcrosses and F2-hybrids gave a weak evidence that genes located in or closely linked to the H-2 complex do influence the spontaneously developed high blood pressure in the NZB/Cr strain of mice. It is emphasized that further studies in larger populations of mice is necessary to establish the importance of linkage of genes to the H-2 comlex for the spontaneous hypertension in the NZB/Cr strain of mice.

小鼠NZB/Cr株自发性高血压的遗传控制。免疫遗传的因素。
NZB/Cr小鼠自发产生高血压。这种高血压发生在婴儿出生后的头两个月。NZB/Cr和C57/B1/6J(一种不会自发产生高血压的正常小鼠品系)之间的f1杂交种也会产生高血压,这表明这种现象是作为显性性状遗传的。对表现型高血压反应的基因位于小鼠MHC (H-2复合体)之外。然而,回交和f2杂交种的H-2分型提供了一个微弱的证据,即位于H-2复合体中或与H-2复合体密切相关的基因确实影响了NZB/Cr小鼠自发性高血压。因此,有必要在更大的小鼠群体中进行进一步的研究,以确定基因与H-2复合物的连锁在小鼠NZB/Cr株自发性高血压中的重要性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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