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[Mapping of the ceruloplasmin gene on human and laboratory mouse chromosomes by direct in situ hybridization].

作者信息

Baranov V S, Shvartsman A L, Gorbunova V N, Gaĭtskhoki V S, Neĭfakh S A

出版信息

Genetika. 1985 Mar;21(3):409-19.

PMID:3886485
Abstract

Mapping of ceruloplasmin gene in human and mouse chromosomes was carried out using the cloned fragments of rat chromosomal ceruloplasmin gene and of ceruloplasmin cDNA as specific hybridization probes. DNA probes were nick-translated with 125I-dCTP up to the high specific capacity. The number of silver grains as well as their distribution along the differentially stained chromosomes were analyzed in 120 metaphase plates from bone marrow cells of laboratory mice and in 181 plates from human lymphocyte cultures. The most probable localization of human ceruloplasmin gene is centromeric region q11-13 of chromosome 15(14?). In laboratory mice ceruloplasmin gene is assigned to the euchromatic part of D-disc of chromosome 9. The possible causes for gene synteny in laboratory mouse and in man as well as its evolutionary implication are discussed.

摘要

相似文献

1
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Genetika. 1985 Mar;21(3):409-19.
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引用本文的文献

1
Chromosomal localization of ceruloplasmin and transferrin genes in laboratory rats, mice and in man by hybridization with specific DNA probes.通过与特异性DNA探针杂交对实验室大鼠、小鼠及人类中铜蓝蛋白和转铁蛋白基因进行染色体定位。
Chromosoma. 1987;96(1):60-6. doi: 10.1007/BF00285885.
2
Comparative map for mice and humans.小鼠与人类的比较图谱。
Mamm Genome. 1992;3(9):480-536. doi: 10.1007/BF00778825.