Mc. Muhlmanndiaz et Js. Bedford, BREAKAGE OF HUMAN-CHROMOSOME-4, HUMAN-CHROMOSOME-19 AND HUMAN-CHROMOSOME-Y IN G(0) CELLS IMMEDIATELY AFTER EXPOSURE TO GAMMA-RAYS, International journal of radiation biology, 65(2), 1994, pp. 165-173
Citations number
32
Categorie Soggetti
Radiology,Nuclear Medicine & Medical Imaging","Nuclear Sciences & Tecnology
One of several possible explanations for the fact that the initial num
ber of ionizing radiation-induced DNA double-strand breaks (dsbs) per
cell per Gy appears to be similar to 5-10 times greater than the numbe
r of excess fragments produced in prematurely condensed chromosomes (P
CCs) is that dsbs in DNA tightly associated with protein, such as migh
t be the case for heterochromatin, are held together and not expressed
as discontinuities in the PCC assay. To test this idea the breakage f
requencies in chromosome 4, 19 and the heterochromatic and more euchro
matic portions of the Y chromosome of non-cycling human fibroblasts we
re measured and compared over a wide range of doses by inducing PCC im
mediately after irradiation with Cs-137 gamma-rays. Even for doses up
to 400 Gy no evidence was seen that Y heterochromatin or large fragmen
ts of it remained unbroken. The only significant deviation from the ex
pected initial breakage frequency per Gy per unit length of chromosome
, in the dose range where a genome average for all chromosomes could b
e obtained, was that observed for the euchromatic portion of the Y chr
omosome (Y p+cen-->q11.2) where breakage was nearly twice that expecte
d. There was no correlation between breakage per unit length and the (
A+T)/(G+C) ratio for these chromosomes or regions.