Difference between revisions of "YDL164C"
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| + | Specifically higher expression in carbon limited chemostat cultures versus carbon excess. | ||
| + | <ref>Boer VM, et al. (2003) The genome-wide transcriptional responses of Saccharomyces cerevisiae grown on glucose in aerobic chemostat cultures limited for carbon, nitrogen, phosphorus, or sulfur. | ||
| + | J Biol Chem 278(5):3265-74</ref> | ||
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Revision as of 13:02, 21 February 2007
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| Systematic name | YDL164C |
| Gene name | CDC9 |
| Aliases | MMS8 |
| Feature type | ORF, Verified |
| Coordinates | Chr IV:167255..164988 |
Description of YDL164C: DNA ligase found in the nucleus and mitochondria, an essential enzyme that joins Okazaki fragments during DNA replication; also acts in nucleotide excision repair, base excision repair, and recombination[1][2][3][4][5][6]
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Contents
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References
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- ↑ Lindahl T and Barnes DE (1992) Mammalian DNA ligases. Annu Rev Biochem 61():251-81 SGD PMID 1497311
- ↑ Waga S and Stillman B (1998) The DNA replication fork in eukaryotic cells. Annu Rev Biochem 67():721-51 SGD PMID 9759502
- ↑ Wu X, et al. (1999) DNA ligation during excision repair in yeast cell-free extracts is specifically catalyzed by the CDC9 gene product. Biochemistry 38(9):2628-35 SGD PMID 10052932
- ↑ Johnston LH and Nasmyth KA (1978) Saccharomyces cerevisiae cell cycle mutant cdc9 is defective in DNA ligase. Nature 274(5674):891-3 SGD PMID 355897
- ↑ Willer M, et al. (1999) The yeast CDC9 gene encodes both a nuclear and a mitochondrial form of DNA ligase I. Curr Biol 9(19):1085-94 SGD PMID 10531002
- ↑ Zou H and Rothstein R (1997) Holliday junctions accumulate in replication mutants via a RecA homolog-independent mechanism. Cell 90(1):87-96 SGD PMID 9230305
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