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小鼠色素突变体ruby-eye、ruby-eye-2-J和栗色中肾脏溶酶体酶分泌的改变

Altered secretion of kidney lysosomal enzymes in the mouse pigment mutants ruby-eye, ruby-eye-2-J, and maroon.

作者信息

Novak E K, Wieland F, Jahreis G P, Swank R T

出版信息

Biochem Genet. 1980 Jun;18(5-6):549-61. doi: 10.1007/BF00484401.

Abstract

Melanosomes and lysosomes share structural and biosynthetic properties. Three mouse pigment mutants, ruby-eye, ruby-eye-2-J, and maroon, have abnormally high concentrations of kidney lysosomal enzymes. concentrations of kidney nonlysosomal enzymes and of liver and serum lysosomal enzymes are normal. By light microscopy the mutants have normal kidney lysosome morphology. It does not appear that the mutant genes cause an increased rate of production of lysosomes since the increased kidney beta-glucuronidase concentration is not accompanied by a corresponding increase in rate of synthesis. The common defect in all mutants is a decreased rate of secretion of lysosomal enzymes from kidney into urine. Eight mouse pigment mutants are not known which affect both melanosome and lysosome function. They should serve as useful models for the study of the biogenesis, structure, and processing of these and other subcellular organelles.

摘要

黑素小体和溶酶体具有共同的结构和生物合成特性。三种小鼠色素突变体,即红宝石眼、红宝石眼-2-J和栗色,其肾脏溶酶体酶浓度异常高。肾脏非溶酶体酶以及肝脏和血清溶酶体酶的浓度正常。通过光学显微镜观察,这些突变体的肾脏溶酶体形态正常。由于肾脏β-葡萄糖醛酸酶浓度升高并未伴随着合成速率的相应增加,因此突变基因似乎并未导致溶酶体产生速率增加。所有突变体的共同缺陷是肾脏溶酶体酶向尿液中的分泌速率降低。已知有八种小鼠色素突变体影响黑素小体和溶酶体的功能。它们应可作为研究这些及其他亚细胞器的生物发生、结构和加工的有用模型。

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