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[Cancer Research 50, 3141-3145, June 1, 1990]
© 1990 American Association for Cancer Research

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An Abnormal Profile of DNA Replication Intermediates in Bloom's Syndrome1

Ulf Lönn2, Sigrid Lönn, Urban Nylen, Gerard Winblad and James German

Radiumhemmet, Karolinska Hospital [U. L., S. L., U. N., G. W.], Department of Histology, Karolinska Institute [U. L., S. L], and Laboratory of Human Genetics, The New York Blood Center, New York, New York [J. G.]

Bloom's syndrome (BS) cells display a characteristic genomic instability, notably an elevated frequency of sister-chromatid exchange. Replicating DNA in cultured BS cells was labeled with [3H]thymidine using several time schedules. Separation of DNA in agarose gels showed high molecular weight DNA and three classes of DNA replication intermediates: 20-kilobase DNA, 10-kilobase DNA, and Okazaki fragments. In contrast newly replicated DNA from normal cells showed no 20-kilobase DNA replication intermediates. Certain BS cells, exceptional in that their characteristic genomic instability has for unknown reasons been corrected, also differed from normal cells in having the 20-kilobase intermediate, but they differed from both normal cells and the other (the uncorrected) BS cells in lacking the 10-kilobase DNA replication intermediates.

1 This work was supported by grants from the King Gustaf V:s Jubilee Foundation, Karolinska Institute, and research grant HD04134 from the NIH.

2 To whom requests for reprints should be addressed, at Radiumhemmet, Karolinska Hospital, PO Box 60500, S-104 01 Stockholm, Sweden.

Received 7/28/89. Revised 1/ 4/90.


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HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Cancer Research Clinical Cancer Research
Cancer Epidemiology Biomarkers & Prevention Molecular Cancer Therapeutics
Molecular Cancer Research Cancer Prevention Research
Cancer Prevention Journals Portal Cancer Reviews Online
Annual Meeting Education Book Meeting Abstracts Online
Copyright © 1990 by the American Association for Cancer Research.