๐”– Bobbio Scriptorium
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Use of fluorescent in situ hybridization to detect chromosomal rearrangements in somatic cell hybrids

โœ Scribed by Dr. Amato J. Giaccia; James W. Evans; J. Martin Brown


Publisher
John Wiley and Sons
Year
1990
Tongue
English
Weight
364 KB
Volume
2
Category
Article
ISSN
1045-2257

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โœฆ Synopsis


In situ hybridization of hamsterlhuman hybrids with biotinylated human genomic D N A has revealed that human chromosomal DNA can integrate into the hamster genome and is not always cytologically detectable. This finding helps t o explain why discordancy can arise in gene mapping by failing to recognize small pieces of foreign DNA in the rodent genome. Fluorescent in situ hybridization allows one t o locate these fragments in rodent chromosomes visually and possibly to identify their chromosome of origin.


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Fig. 1. a: Representative GTG-banded chromosome 15s demonstrating lack of a detectable deletion, b: representative cell from FISH analysis demonstrating the normal signal pattern for SNRPN found in 11/39 cells, and c: Representative cell from the same FISH analysis demonstrating a deletion of SNRPN