Analysis of DNA sequences homologous with the ARS core consensus in Saccharomyces cerevisiae
- 1 June 1987
- Vol. 3 (2) , 107-115
- https://doi.org/10.1002/yea.320030207
Abstract
We have previously identified an autonomously replicating segment (ARS) near the 3′ end of the histone H4 gene at the copy‐I H3‐H4 locus. We have now searched for additional autonomously replicating segments and sequences homologous with the ARS core consensus sequence near the copy‐II histone H4 gene and both of the histone H3 genes. No new ARS elements were identified by functional cloning assays. However, several matches to the ARS core consensus element were found within the DNA sequencs of the copy‐I and copy‐II genes. An exact match to the ARS core consensus was identified in the region downstream from the copy‐I histone H3 gene and a set of sequences with weak homology was also locatd within the copy‐II region. However, restriction fragments including these sequences did not demonstrate ARS activity on a plasmid in transformed cells.Keywords
This publication has 38 references indexed in Scilit:
- Detection of specific sequences among DNA fragments separated by gel electrophoresisPublished by Elsevier ,2006
- Regulation of mating-type information in yeastJournal of Molecular Biology, 1984
- Structural requirements for the function of a yeast chromosomal replicatorCell, 1984
- DNA sequences of yeast H3 and H4 histone genes from two non-allelic gene sets encode identical H3 and H4 proteinsJournal of Molecular Biology, 1983
- Yeast H3 and H4 histone messenger RNAs are transcribed from two non-allelic gene setsJournal of Molecular Biology, 1983
- Isolation of chromosomal origins of replication in yeastNature, 1980
- Isolation of yeast histone genes H2A and H2BCell, 1979
- Sterile host yeasts (SHY): A eukaryotic system of biological containment for recombinant DNA experimentsGene, 1979
- Molecular cloning of the DNA ligase gene from bacteriophage T4Journal of Molecular Biology, 1979
- Labeling deoxyribonucleic acid to high specific activity in vitro by nick translation with DNA polymerase IJournal of Molecular Biology, 1977