Chem.-BioL Interactions, 74 (1990) 2 0 7 - 220 207
Elsevier Scientific Publishers Ireland Ltd.
EFFECT OF N-METHYL-N-NITROSOUREA ON AVIAN
ERYTHROCYTE NUCLEI REACTIVATION
S.P. GUY', T.K. BRADSHAWb and RUTH F. ITZHAKP.*
"Molecular Neurobiology Laboratory, Department of Optometry and Vision Sciences, UMIST,
P.O. Box 88, Manchester, M60 1QD and bSheU Research Limited, Sittingbourne, Kent, ME9 SAG
(U.K.)
(Received August 17th, 1989)
(Revision received November 6th, 1989)
(Accepted November 20th, 1989)
SUMMARY
Avian erythrocytes are terminally differentiated cells but they can be
reactivated by fusion with actively metabolising cells. We have examined the
effects of treating the erythrocytes with a carcinogenic methylating agent,
N-methyl-N-Nitrosourea (MNU), on the process of reactivation of adult and
embryonic nuclei. We have found that the rate of nuclear enlargement is
slightly lower in nuclei from MNU-treated cells than from control cells and
that there is a marked delay of about 24 h in the appearance of nucleoli in
both adult and embryonic cells. This is not due to an effect of MNU on ribo-
somal (r)DNA: the number of rDNA genes appears to be similar in treated
and control cells. Also, the number of rDNA genes appears to be similar in
adult and embryonic cells and in unreactivated and reactivated embryonic
nuclei: thus, differences in reactivation rate between adult and embryonic
cells, observed by us and others, can not be attributed to a gross difference
in their ribosomal DNA contents, and reappearance of nucleoli on reactiva-
tion can not be due to an amplification of rDNA (i.e., to recovery of such
genes if lost on terminal differentiation). We suggest that MNU, although a
monofunctional alkylating agent, may cause increased association -- possibly
cross-linkage -- between DNA and protein in chromatin, thereby hindering
access of host cell reactivating proteins, especially to the nucleolar regions.
*To whom correspondence should be sent.
Abbreviations: DMSO, dimethylsulphoxide; EBSS, Earle's balanced salt solution; EMEM, Eagle's
minimum essential medium; HAT, hypoxanthine aminopterin thymidine; HGPRT, hypoxanthine-
guanine phosphoribosyl tranferase; MNU, N-methyl-N-nitrosourea; PBS, phosphate-buffered
saline; PCA, perchloric acid; rDNA, ribosomal DNA; RSB, reticulocyte standard buffer; UDS,
uncheduled DNA synthesis.
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© 1990 Elsevier Scientific Publishers Ireland Ltd.
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