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Journal of Clinical Pathology logoLink to Journal of Clinical Pathology
. 1974 Oct;27(10):789–793. doi: 10.1136/jcp.27.10.789

Serum `uracil + uridine' levels in normal subjects and their possible significance

T E Parry 1,2, J A Blackmore 1,2
PMCID: PMC475483  PMID: 4214838

Abstract

A microbiological method for the assay of uracil is described. The growth of the test organism is supported by uracil and also by uridine but not by uridylic acid. The method therefore measures uracil and uridine together. The `uracil + uridine' level, expressed as uracil, has been measured in blood from 144 normal subjects ranging in age from cord blood to the eighth decade. The mean level of 22 μ mol/l (0·25 mg%) in cord blood decreases to 15 μmol/l (0·17 mg%) in adults over the age of 20. There is no difference between the sexes.

Uracil is of interest because (a) it is a constituent base of RNA, (b) it is the precursor of two of the bases thymine and cytosine that enter into the composition of DNA, and (c) under certain circumstances it has mutagenic properties. The last is dependent upon the existence of two tautomeric forms of uracil, the common keto form which pairs normally with adenine and the rare enol form which pairs with guanine. A mistake in base pairing which allows uracil in its enol form to enter the DNA molecule and pair with guanine can result in a G = C → A = T base transition in the DNA molecule. The molecular mechanism involved as well as the possible bearing on somatic mutation are discussed.

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Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. BURNET M. SOMATIC MUTATION AND CHRONIC DISEASE. Br Med J. 1965 Feb 6;1(5431):338–342. doi: 10.1136/bmj.1.5431.338. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. Blackmore J. A., Parry T. E. Microbiological assay of amino acids in serum: valine, leucine, and methionine. J Clin Pathol. 1972 Feb;25(2):171–175. doi: 10.1136/jcp.25.2.171. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. COMFORT A. Mutation, autoimmunity, and ageing. Lancet. 1963 Jul 20;2(7299):138–141. doi: 10.1016/s0140-6736(63)92602-3. [DOI] [PubMed] [Google Scholar]
  4. FREESE E. On the molecular explanation of spontaneous and induced mutations. Brookhaven Symp Biol. 1959 Nov;NO:63–75. [PubMed] [Google Scholar]

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