PMID: 6112733Mar 11, 1981Paper

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

Nucleic Acids Research
I BozzoniF Amaldi

Abstract

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.

References

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Citations

Oct 1, 1985·Developmental Biology·E Z Baum, W M Wormington
Jan 1, 1987·Molecular and Cellular Endocrinology·L J Holland, L J Wangh
Sep 1, 1986·Proceedings of the National Academy of Sciences of the United States of America·I T ChenD J Roufa
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Nov 1, 1986·Proceedings of the National Academy of Sciences of the United States of America·W M Wormington
Aug 11, 1982·Nucleic Acids Research·M PiechaczykP Jeanteur
Oct 11, 1982·Nucleic Acids Research·S Fabijanski, M Pellegrini
Jul 11, 1984·Nucleic Acids Research·P O O'Connell, M Rosbash
Jul 25, 1985·Nucleic Acids Research·R J LeerR J Planta
Jun 10, 1988·Nucleic Acids Research·F RaftiF Graziani
Aug 11, 1981·Nucleic Acids Research·B WestleyR Weber
Sep 1, 1982·European Journal of Biochemistry·W Y ChooiD K Burns
Sep 25, 1982·Journal of Molecular Biology·A ColmanG Valle
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Jan 25, 1988·Biochimica Et Biophysica Acta·W H Mager
Jul 13, 1988·Biochimica Et Biophysica Acta·J E DurbinA M Fallon

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