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小鼠中磷酸化酶b激酶的遗传方式

Phosphorylase b kinase inheritance in mice.

作者信息

Lyon J B, Porter J, Robertson M

出版信息

Science. 1967 Mar 24;155(3769):1550-1. doi: 10.1126/science.155.3769.1550.

DOI:10.1126/science.155.3769.1550
PMID:6020474
Abstract

The gene for phosphoryl ase b kinase, a skeletal muscle enzyme, has been located on the X chromo some of mice. The inheritance of the enzyme through two generations from original matings between one inbred strain of mice, the I, which lacks the enzyme, and another strain, the C(57,) follows the classical Mendelian pattern.

摘要

磷酸化酶b激酶是一种骨骼肌酶，其基因已定位在小鼠的X染色体上。该酶从一个缺乏该酶的近交系小鼠I与另一个品系C（57）的原始交配开始，经过两代的遗传遵循经典的孟德尔模式。

相似文献

1
Phosphorylase b kinase inheritance in mice.小鼠中磷酸化酶b激酶的遗传方式
Science. 1967 Mar 24;155(3769):1550-1. doi: 10.1126/science.155.3769.1550.
2
In vivo response of skeletal muscle glycogen phosphorylase, phosphorylase b kinase and cyclic AMP to epinephrine administration.骨骼肌糖原磷酸化酶、磷酸化酶b激酶及环磷酸腺苷对肾上腺素给药的体内反应。
Biochem Biophys Res Commun. 1962 Oct 31;9:293-6. doi: 10.1016/0006-291x(62)90042-6.
3
Epinephrine induced formation of adenosine 3', 5'-monophosphate in mouse skeletal muscle.
Biochem Biophys Res Commun. 1969 Feb 21;34(4):459-64. doi: 10.1016/0006-291x(69)90404-5.
4
Stimulation of glycogenolysis by beta adrenergic agonists in skeletal muscle of mice with the phosphorylase kinase deficiency mutation (I strain).在具有磷酸化酶激酶缺陷突变的小鼠（I 品系）骨骼肌中，β肾上腺素能激动剂对糖原分解的刺激作用。
J Pharmacol Exp Ther. 1976 Sep;198(3):526-38.
5
X-linked dominant inheritance of partial phosphorylase kinase deficiency in mice.小鼠部分磷酸化酶激酶缺乏症的X连锁显性遗传
Biochem Genet. 1980 Apr;18(3-4):247-61. doi: 10.1007/BF00484240.
6
EFFECTS OF ELECTRICAL STIMULATION AND EPINEPHRINE ON MUSCLE PHOSPHORYLASE, PHOSPHORYLASE B KINASE, AND ADENOSINE 3',5'-PHOSPHATE.电刺激和肾上腺素对肌肉磷酸化酶、磷酸化酶B激酶及腺苷3',5'-磷酸的影响
J Biol Chem. 1965 Mar;240:982-5.
7
Loss of cyclic 3'5'-AMP dependent kinase and reduction of phosphorylase kinase in skeletal muscle of a girl with deactivated phosphorylase and glycogenosis of liver and muscle.一名患有磷酸化酶失活及肝和肌肉糖原贮积症的女孩，其骨骼肌中依赖环3',5'-AMP的激酶缺失，磷酸化酶激酶减少。
Biochem Biophys Res Commun. 1970 Aug 24;40(4):982-8. doi: 10.1016/0006-291x(70)91000-4.
8
Phosphorylase kinase deficiency.磷酸化酶激酶缺乏症。
Biochem Genet. 1970 Feb;4(1):187-94. doi: 10.1007/BF00484029.
9
The X-chromosome and the enzymes controlling muscle glycogen: phosphorylase kinase.X染色体与控制肌肉糖原的酶：磷酸化酶激酶。
Biochem Genet. 1970 Feb;4(1):169-85. doi: 10.1007/BF00484028.
10
Requirement of Ca ion for the stimulating effect of cyclic 3',5'-AMP on muscle phosphorylase b kinase.钙离子对环3',5'-腺苷酸刺激肌肉磷酸化酶b激酶作用的需求
J Biochem. 1967 Aug;62(2):285-6. doi: 10.1093/oxfordjournals.jbchem.a128663.

引用本文的文献

1
Metabolic Systems and the Inherited Diseases of Man.代谢系统与人类遗传性疾病
J R Coll Physicians Lond. 1968 Oct;3(1):5-24.
2
X-linked dominant inheritance of partial phosphorylase kinase deficiency in mice.小鼠部分磷酸化酶激酶缺乏症的X连锁显性遗传
Biochem Genet. 1980 Apr;18(3-4):247-61. doi: 10.1007/BF00484240.
3
Inherited metabolic disease in laboratory animals: a review.实验动物中的遗传性代谢疾病：综述
J Inherit Metab Dis. 1980;3(4):133-43. doi: 10.1007/BF02312547.
4
Glycogen storage diseases in animals and their potential value as models of human disease.动物中的糖原贮积病及其作为人类疾病模型的潜在价值。
J Inherit Metab Dis. 1983;6(1):3-16. doi: 10.1007/BF02391186.
5
Phosphorylase kinase deficiency.磷酸化酶激酶缺乏症。
Biochem Genet. 1970 Feb;4(1):187-94. doi: 10.1007/BF00484029.
6
The X-chromosome and the enzymes controlling muscle glycogen: phosphorylase kinase.X染色体与控制肌肉糖原的酶：磷酸化酶激酶。
Biochem Genet. 1970 Feb;4(1):169-85. doi: 10.1007/BF00484028.
7
Linkage analyses using biochemical variants in mice. 3. Linkage relationships of eleven biochemical markers.利用小鼠生化变异进行连锁分析。3. 11种生化标记的连锁关系。
Biochem Genet. 1970 Apr;4(2):339-50. doi: 10.1007/BF00485782.
8
X-chromosomal inheritance of liver glycogenosis with phosphorylase kinase deficiency.伴有磷酸化酶激酶缺乏的肝糖原贮积症的X染色体遗传。
Am J Hum Genet. 1969 May;21(3):275-84.
9
Location of phosphorylase kinase (Phk) in the mouse X chromosome.磷酸化酶激酶（Phk）在小鼠X染色体中的定位。
Biochem Genet. 1973 Jun;9(2):193-6. doi: 10.1007/BF00487449.
10
Glucose-6-phosphatase deficiency caused by radiation-induced alleles at the albino locus in the mouse.小鼠白化病基因座处辐射诱导等位基因导致的葡萄糖-6-磷酸酶缺乏症。
Proc Natl Acad Sci U S A. 1968 Feb;59(2):437-44. doi: 10.1073/pnas.59.2.437.