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Sister chromatid exchange
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Sister chromatid exchange : ウィキペディア英語版
Sister chromatid exchange

Sister chromatid exchange (SCE) is the exchange of genetic material between two identical sister chromatids.
It was first discovered by using the Giemsa staining method on one chromatid belonging to the sister chromatid complex before anaphase in mitosis. The staining revealed that few segments were passed to the sister chromatid which were not dyed.
The Giemsa staining was able to stain due to the presence of bromodeoxyuridine analogous base which was introduced to the desired chromatid.
The reason for the (SCE) is not known but it is required and used as a mutagenic testing of many products. Four to five sister chromatid exchange per chromosome pair, per mitosis is in the normal distribution, 14-100 exchanges is not normal and presents a danger to the organism. SCE is elevated in pathologies including Bloom syndrome, having recombination rates ~10-100 times above normal, depending on cell type. Frequent SCEs may also be related to formation of tumors.
Sister chromatid exchange has also been observed more frequently in B51(+) Behçet's disease.
==Mitosis==
Mitotic recombination in the budding yeast ''Saccharomyces cerevisiae'' is primarily a result of DNA repair processes responding to spontaneous or induced damages that occur during vegetative growth.} (Also reviewed in Bernstein and Bernstein, pp 220–221). In order for yeast cells to repair damage by homologous recombination, there must be present, in the same nucleus, a second DNA molecule containing sequence homology with the region to be repaired. In a diploid cell in G1 phase of the cell cycle, such a molecule is present in the form of the homologous chromosome. However, in the G2 phase of the cell cycle (following DNA replication), a second homologous DNA molecule is also present: the sister chromatid. Evidence indicates that, due to the special nearby relationship they share, sister chromatids are not only preferred over distant homologous chromatids as substrates for recominational repair, but have the capacity to repair more DNA damage than do homologs.

抄文引用元・出典: フリー百科事典『 ウィキペディア(Wikipedia)
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