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PMID: 6956858 Published · ppublish English Journal Article Research Support, U.S. Gov't, P.H.S.

Partial purification and characterization of the mRNA for human thymidine kinase and hypoxanthine/guanine phosphoribosyltransferase.

Lin PF, Yamaizumi M, Murphy PD, Egg A, Ruddle FH

Abstract

We used direct microinjection of poly(A)+RNA into individual hypoxanthine/guanine phosphoribosyltransferase-deficient or thymidine kinase-deficient cells and detected the specific in vivo translation products as an assay for human hypoxanthine/guanine phosphoribosyltransferase or thymidine kinase mRNAs. The incorporation of [3H]hypoxanthine or [3H]thymidine into cells in response to injected mRNA was assayed in situ by autoradiography. Methylmercuric hydroxide/agarose gel analysis showed that human hypoxanthine/guanine phosphoribosyltransferase mRNA contains approximately 1,530 nucleotides, which is twice the number required for its protein coding capacity. The mRNA for human cytoplasmic thymidine kinase is estimated to be approximately the same length; thus, the size of the cytosol thymidine kinase subunit can be predicted to be approximately 47,000 daltons, if the full coding capacity of its mRNA is utilized.

MeSH Terms
Biological Assay Humans Hypoxanthine Phosphoribosyltransferase/genetics Molecular Weight Protein Biosynthesis RNA, Messenger/isolation & purification Thymidine Kinase/genetics
Chemicals
RNA, Messenger Hypoxanthine Phosphoribosyltransferase Thymidine Kinase
Authors & Affiliations
5 authors, click to expand affiliations / ORCID
Lin P F
Yamaizumi M
Murphy P D
Egg A
Ruddle F H
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42 references, click to expand
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Article Info
Journal
Proceedings of the National Academy of Sciences of the United States of America
Abbr.
Proc Natl Acad Sci U S A
ISSN
0027-8424
Published
1982-07-00
Pages
4290-4
Language
English
Region
United States
NLM ID
7505876
PMCID
PMC346656
Subset
IM
Grants
NIA NIH HHS · 5 R01 AGD1940-02 · United States
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