Hereditary nonpolyposis colon cancer (HNPCC) is an autosomal dominantly inherited cancer predisposition which is linked to heterozygous mutations in mismatch repair genes. HNPCC tumour cells, in which the remaining wild-type copy of the mismatch repair gene is inactivated, display instability of mic
Mismatch repair in mammalian cells
β Scribed by Louise A. Heywood; Julian F. Burke
- Publisher
- John Wiley and Sons
- Year
- 1990
- Tongue
- English
- Weight
- 605 KB
- Volume
- 12
- Category
- Article
- ISSN
- 0265-9247
No coin nor oath required. For personal study only.
β¦ Synopsis
A vital process in maintaining a low genetic error rate is the removal of mismatched bases in DNA. The importance of this process in E. coli is demonstrated by the 100-1000 fold increase in mutation frequency observed in cells deficient in this repair system"'. Mismatches can arise as a consequence of recombination, errors in replication and as a result of spontaneous chemical deamination, the latter process resulting in an estimated twelve T:G mismatches per genome per day in mammalian celld2'. Recent studies, discussed here, provide evidence for the existence of specific mismatch repair systems in mammalian and human cells.
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