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PMID: 10577395 Published · epublish English Journal Article Review

Replication origins of mammalian chromosomes: the happy few.

Frontiers in bioscience : a journal and virtual library ·Vol. 4 ·1999-12-01 ·Pages D859-68

Todorovic V, Falaschi A, Giacca M

Abstract

Replication of eukaryotic cell genomes is a tightly controlled process occurring once and only once per cell cycle. Replication initiates at several thousand origins, whose cis-acting sequences and trans-acting proteins have been partially characterized in the yeast S. cerevisiae in the last few years. In contrast, identification of origins of DNA replication in mammalian cells have proven much more difficult. Currently, less then 20 bona fide mammalian origins have been identified, of which only few characterized in detail. Here we discuss the available methods for origin identification in mammalian DNA and the main results, sometimes controversial, so far generated by their application. In particular, we review the currently available information concerning the three best characterized origins, namely those in the lamin B2 and b-globin gene domains in human cells and the one located downstream of the dihydrofolate reductase gene in hamster cells.

MeSH Terms
Animals Chromosomes/genetics Cricetinae Eukaryotic Cells/metabolism Globins/genetics Humans Lamin Type B Lamins Nuclear Proteins/genetics Replication Origin/genetics Saccharomyces cerevisiae/genetics Tetrahydrofolate Dehydrogenase/genetics
Chemicals
Lamin Type B Lamins Nuclear Proteins lamin B2 Globins Tetrahydrofolate Dehydrogenase
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Todorovic V
Molecular Medicine, International Centre for Genetic Engineering and Biotechnology (ICGEB), Padriciano 99, 34012 Trieste, Italy. [email protected]
Falaschi A
Giacca M
Article Info
Journal
Frontiers in bioscience : a journal and virtual library
Abbr.
Front Biosci
ISSN
1093-9946
Published
1999-12-01
Epub
1999-00-01
Pages
D859-68
Language
English
Region
United States
NLM ID
9709506
Subset
IM
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