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Brain DNA metabolism in myelin deficient mutant jp, jpmsd and qk mice.

作者信息

Shah S N, Johnson R C

出版信息

Neurochem Res. 1983 Dec;8(12):1611-20. doi: 10.1007/BF00964162.

DOI:10.1007/BF00964162
PMID:6672643
Abstract

We studied metabolism of brain DNA in three myelin deficient mutants qk, jp and jpmsd mice. The DNA content, the in vivo incorporation of [14C]thymidine in DNA and the activity of acid DNase in tissues (cerebellum and cerebrum) from normal littermates and affected mice were compared. The results showed that neither the DNA content, the incorporation of [14C]thymidine in DNA nor the activity of acid DNase in brain were altered in qk affected mice. In jpmsd mice, however, the DNA content as well as the incorporation of thymidine in DNA were reduced in both cerebellum and cerebrum, but the activity of acid DNase was reduced in cerebrum only. In jp mice, although the DNA content was reduced in both cerebellum and cerebrum, the incorporation of thymidine in DNA and the activity of acid DNase were reduced in cerebrum only. The data suggest a) that in qk mutants DNA metabolism and hence cell (glial) proliferation is not affected; b) that in jpmsd mutants DNA synthesis, and thus the cell proliferation is reduced in cerebellum as well as in cerebrum of the affected mice and c) that in jp mutants the synthesis of DNA and the cell proliferation is reduced in cerebrum but not in cerebellum.

摘要

相似文献

1
Brain DNA metabolism in myelin deficient mutant jp, jpmsd and qk mice.
Neurochem Res. 1983 Dec;8(12):1611-20. doi: 10.1007/BF00964162.
2
Myelination of jp,jpmsd, and qk axons by normal glia in vitro: ultrastructural and autoradiographic evidence.正常神经胶质细胞在体外对jp、jpmsd和qk轴突的髓鞘形成:超微结构和放射自显影证据。
Brain Res. 1983 Jun 6;268(2):255-66. doi: 10.1016/0006-8993(83)90491-2.
3
Myelin basic protein gene expression in quaking, jimpy, and myelin synthesis-deficient mice.震颤鼠、jimpy鼠和髓鞘合成缺陷型小鼠中髓鞘碱性蛋白基因的表达
Dev Biol. 1984 Nov;106(1):38-44. doi: 10.1016/0012-1606(84)90058-7.
4
Hypomyelinated mutant mice: description of jpmsd and comparison with jp and qk on their present genetic backgrounds.髓鞘形成不足的突变小鼠:jpmsd的描述及其在当前遗传背景下与jp和qk的比较。
Brain Res. 1980 Aug 4;194(2):325-38. doi: 10.1016/0006-8993(80)91215-9.
5
Hypomyelinated mutant mice. II. Myelination in vitro.髓鞘形成不足的突变小鼠。II. 体外髓鞘形成
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6
Shiverer jimpy double mutant mice. III. Comparison of shimld*jpmsd and shi*jp phenotypes demonstrates dissimilar interactions of allelic mutations.颤抖-矮小双突变小鼠。III. 颤抖矮小(shimld*jpmsd)和颤抖*矮小(shi*jp)表型的比较表明等位基因突变的相互作用不同。
Brain Res. 1987 Sep;388(3):199-214.
7
Expression of myelin basic protein genes in several dysmyelinating mouse mutants during early postnatal brain development.出生后早期脑发育过程中几种脱髓鞘小鼠突变体中髓鞘碱性蛋白基因的表达
J Neurochem. 1985 Aug;45(2):572-80. doi: 10.1111/j.1471-4159.1985.tb04025.x.
8
Effect of hyperphenylalaninemia induced during suckling on brain DNA metabolism in rat pups.
Neurochem Res. 1984 Apr;9(4):517-28. doi: 10.1007/BF00964378.
9
Quaking*jimpy double mutant mice: additional evidence for independence of primary deficits in jimpy.
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10
Cell-free synthesis of myelin basic proteins in normal and dysmyelinating mutant mice.正常和脱髓鞘突变小鼠中髓鞘碱性蛋白的无细胞合成
J Neurochem. 1984 Mar;42(3):733-9. doi: 10.1111/j.1471-4159.1984.tb02744.x.

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