## REVIEW ARTICLES cells during serial blast cell divisions in the leech. SOC. Neurosci. Abstr. 11, 649. 11 WEISBLAT, D. A. & SHANKLAND M. (1985). Cell lineage and segmentation in the leech embryo. Proc. Roy. SOC. Series B (in press). 1 2 BLAIR, S. S. (1983). Blastomere ablation and the developmen
Mapping replication origins in yeast chromosomes
β Scribed by Bonita J. Brewer; Walton L. Fangman
- Book ID
- 102759681
- Publisher
- John Wiley and Sons
- Year
- 1991
- Tongue
- English
- Weight
- 740 KB
- Volume
- 13
- Category
- Article
- ISSN
- 0265-9247
No coin nor oath required. For personal study only.
β¦ Synopsis
The replicon hypothesis, first proposed in 1963 by Jacob and Brenner''), states that DNA replication is controlled at sites called origins. Replication origins have been well studied in prokaryotes. However, the study of eukaryotic chromosomal origins has lagged behind, because until recently there has been no method for reliably determining the identity and location of origins from eukaryotic chromosomes. Here, we review a technique we developed with the yeast Saccharomyces cerevisiae that allows both the mapping of replication origins and an assessment of their activity. Two-dimensional agarose gel electrophoresis and Southern hybridization with total genomic DNA are used to determine whether a particular restriction fragment acquires the branched structure diagnostic of replication initiation. The technique has been used to localize origins in yeast chromosomes and assess their initiation efficiency. In some cases, origin activation is dependent upon the surrounding context. The technique is also being applied to a variety of eukaryotic organisms.
π SIMILAR VOLUMES
The process by which eukaryotic cells decide when and where to initiate DNA replication has been illuminated in yeast, where specific DNA sequences (replication origins) bind a unique group of proteins (origin recognition complex) next to an easily unwound DNA sequence at which replication can begin
## Abstract **Background:** Understanding of the firing time determination of replication origins in the entire genome will require a genomeβwide survey of replication origins and their mapping on chromosomes. A microarray technology was applied to obtain a genomeβwide profile of DNA replication an