Xenopus laevis ribosomal protein genes: isolation of recombinant cDNA clones and study of the genomic organization.

Xenopus laevis ribosomal protein genes: isolation of recombinant cDNA clones and study of the genomic organization.
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非洲爪蟾核糖体蛋白基因:重组 cDNA 克隆的分离和基因组组织的研究。

DOI:
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发表时间:
1981
影响因子:
14.9
通讯作者:
F. Amaldi
F. Amaldi
中科院分区:
生物学2区
文献类型:
--
作者:
I. Bozzoni;E. Beccari;Z. Luo;F. Amaldi

文献摘要

被引文献

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来自非洲爪蟾卵母细胞的Poly-A+ mRNA,部分富集了r-蛋白编码能力,已被用作在质粒pBR 322中制备cDNA库的起始材料。已通过翻译互补mRNA选择了含有对r-蛋白特异性序列的克隆。六种不同的r-蛋白的克隆已被鉴定并用作研究其基因组组织的探针。每个单倍体基因组中发现两个基因拷贝的r-蛋白L1,L14,S19,和4 - 5蛋白S1,S8和L32。此外,已观察到含有r-蛋白S1、S8和L14序列的基因组区域的群体多态性。
Poly-A+ mRNA from Xenopus laevis oocytes, partially enriched for r-protein coding capacity has been used as starting material for preparing a cDNA bank in plasmid pBR322. The clones containing sequences specific for r-proteins have been selected by translation of the complementary mRNAs. Clones for six different r-proteins have been identified and utilized as probes for studying their genomic organization. Two gene copies per haploid genome were found for r-proteins L1, L14, S19, and four-five for protein S1, S8 and L32. Moreover a population polymorphism has been observed for the genomic regions containing sequences for r-protein S1, S8 and L14.