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小鼠急性期蛋白的遗传学与进化

Genetics and evolution of the acute phase proteins in mice.

作者信息

Baumann H, Berger F G

出版信息

Mol Gen Genet. 1985;201(3):505-12. doi: 10.1007/BF00331347.

Abstract

In mammals, a number of liver-derived plasma proteins, termed acute phase reactants, are induced during an inflammation response. We have studied genetic variation in the structure and expression of several of these proteins in a variety of inbred and wild-derived mice. In a genetic cross, electrophoretic polymorphisms for the two alpha 1-acid glycoproteins, AGP-1 and AGP-2, co-segregated in 58 backcross progeny, indicating that either a single gene or two tightly-linked genes on chromosome 4 encode the AGPs. In the same backcross, segregation of variation in haptoglobin structure showed that the gene encoding this acute phase reactant is on chromosome 8. Structural variation in serum amyloid A correlated with restriction fragment length polymorphisms in the Saa gene determined by Taylor and Rowe (1984). Analysis of a number of highly diverged species of mice indicated that AGP expression has undergone considerable modification during evolution of the Mus genus; this is associated with alterations in Agp gene organization, which may include species-specific amplification and/or deletion events.

摘要

在哺乳动物中,一些源自肝脏的血浆蛋白,即急性期反应物,在炎症反应期间被诱导产生。我们研究了多种近交系和野生衍生小鼠中这些蛋白中几种蛋白的结构和表达的遗传变异。在一次遗传杂交中,两种α1-酸性糖蛋白AGP-1和AGP-2的电泳多态性在58个回交后代中共分离,这表明位于4号染色体上的一个基因或两个紧密连锁的基因编码这些AGP。在同一回交中,触珠蛋白结构变异的分离表明,编码这种急性期反应物的基因位于8号染色体上。血清淀粉样蛋白A的结构变异与泰勒和罗(1984年)确定的Saa基因中的限制性片段长度多态性相关。对一些高度分化的小鼠物种的分析表明AGP表达在小家鼠属进化过程中经历了相当大的修饰;这与Agp基因组织的改变有关,其中可能包括物种特异性扩增和/或缺失事件。

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