Tc. Hsu et al., MUTAGEN SENSITIVITY IN HUMANS - A COMPARISON BETWEEN 2 NOMENCLATURE SYSTEMS FOR RECORDING CHROMATID BREAKS, Cancer genetics and cytogenetics, 87(2), 1996, pp. 127-132
Currently, there are two systems in use for recording chromatid breaks
, either spontaneously occurring or induced by mutagens: The Internati
onal System for Human Cytogenetic Nomenclature (ISCN) and the Chatham
Barrs Inn Conference (CBIC) recommendation. The former system consider
s that a chromatid break is recognized only when the chromatid fragmen
t is displaced to the other side of its sister chromatid, while all ot
hers, regardless of the distance between the two broken ends, are call
ed chromatid gaps. The CBIC system recognizes a chromatid break when t
he intervening achromatic segment is longer than or equal to the diame
ter of the chromatid, whether the fragment is displaced or not. Minor
lesions are called chromatid gaps. We conducted experiments using bleo
mycin treatment of human cells (primary cultures or lymphoblastoid cel
l lines) and read the chromatid lesions both ways. We conclude that th
e CBIC system appears to have more direct biologic relevance than the
ISCN system.