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小鼠肝脏中主要尿蛋白合成的遗传变异研究。

Studies on genetic variation in major urinary protein synthesis in mouse liver.

作者信息

Berger F G

出版信息

Biochem Genet. 1983 Feb;21(1-2):15-23. doi: 10.1007/BF02395388.

Abstract

A two- to fourfold difference in the relative rate of total major urinary protein (MUP) synthesis between C57BL/6J and C3H/HeJ female mice has been analyzed at the genetic and molecular levels. The C57BL/6J phenotype is dominant in F1 female progeny of a cross between the two strains. Quantitation of MUP mRNA levels indicates that the rate of synthesis variation does not reflect a change in the concentration of total MUP mRNA. In recombinant inbred strains derived from C57BL/6J and C3H/HeJ progenitors, the rate of synthesis difference segregates as a single genetic determinant that is not linked to the Mup-a locus on chromosome 4. The results suggest an unlinked locus that acts to alter total MUP synthesis without altering total MUP mRNA levels. Two models are proposed to describe the action of this locus, both of which imply some sort of posttranscriptional control of MUP synthesis.

摘要

已在基因和分子水平上分析了C57BL/6J和C3H/HeJ雌性小鼠之间总主要尿蛋白(MUP)合成相对速率的两到四倍差异。C57BL/6J表型在这两个品系杂交的F1雌性后代中占主导地位。MUP mRNA水平的定量分析表明,合成速率的变化并不反映总MUP mRNA浓度的改变。在源自C57BL/6J和C3H/HeJ亲本的重组近交系中,合成速率差异作为一个单一的遗传决定因素进行分离,该因素与4号染色体上的Mup-a位点不连锁。结果表明存在一个不连锁的位点,该位点可改变总MUP合成而不改变总MUP mRNA水平。提出了两种模型来描述该位点的作用,这两种模型都暗示了对MUP合成的某种转录后控制。

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