scholarly journals Segregation of DNA polynucleotide strands into sister chromatids and the use of endoreduplicated cells to track sister chromatid exchanges induced by crosslinks, alkylations, or x-ray damage.

1996 ◽  
Vol 93 (12) ◽  
pp. 5765-5769 ◽  
Author(s):  
S. Wolff ◽  
V. Afzal
1988 ◽  
Vol 7 (7) ◽  
pp. 975-986
Author(s):  
Richard P. Solana ◽  
Walter H. Carter ◽  
John D. Wilson ◽  
Vernon M. Chinchilli ◽  
Richard A. Carchman

Response surface methodology (RSM), a collection of statistical and mathematical techniques, can empirically model multiple agent interactions. The use of RSM allows modeling of the interaction at all levels of each agent, rather than focusing on a single level of effect, thereby describing the changing interaction present. Further, this technique allows qualitative analysis of the resultant model of the combination exposure for existing interactions. RSM was used in the statistical analysis of sister chromatid exchanges (SCE) elicited by combination exposures of genotoxic agents, ethylnitrosourea (ENU) with cis-diaminedichloroplatinum (II) (DDP), and DDP with x-rays. ENU and DDP each exhibited curvilinear concentration-related increases in SCEs. X-ray exhibited a linear increase in SCEs. For the DDP-x-ray combination, RSM analysis indicates a less-than-additive interaction, suggested by the nonparallel concentration-response curves of one agent at varying concentrations of the other. For the DDP-ENU combination, an increasingly less-than-additive interaction was detected. This descriptive ability is shown to be useful in suggesting hypotheses about mechanisms of action. Employing a polynomial model assumes effect-addition as an underlying assumption of additivity. Models with other underlying assumptions of additivity also can be used.


2016 ◽  
Vol 149 (3) ◽  
pp. 218-225 ◽  
Author(s):  
Veit Schubert ◽  
Mateusz Zelkowski ◽  
Sonja Klemme ◽  
Andreas Houben

Due to the X-shape formation at somatic metaphase, the arrangement of the sister chromatids is obvious in monocentric chromosomes. In contrast, the sister chromatids of holocentric chromosomes cannot be distinguished even at mitotic metaphase. To clarify their organization, we differentially labelled the sister chromatids of holocentric Luzula and monocentric rye chromosomes by incorporating the base analogue EdU during replication. Using super-resolution structured illumination microscopy (SIM) and 3D rendering, we found that holocentric sister chromatids attach to each other at their contact surfaces similar to those of monocentrics in prometaphase. We found that sister chromatid exchanges (SCEs) are distributed homogeneously along the whole holocentric chromosomes of Luzula, and that their occurrence is increased compared to monocentric rye chromosomes. The SCE frequency of supernumerary B chromosomes, present additionally to the essential A chromosome complement of rye, does not differ from that of A chromosomes. Based on these results, models of the sister chromatid arrangement in mono- and holocentric plant chromosomes are presented.


1976 ◽  
Vol 24 (1) ◽  
pp. 168-177 ◽  
Author(s):  
G W Zack ◽  
J A Spriet ◽  
S A Latt ◽  
G H Granlund ◽  
I T Young

Sister chromatids of human metaphase chromsomes from cells which have replicated twice in medium containing 5-bromodeoxyuridine exhibit unequal fluorescence when stained with the dye 33258 Hoechst. Sister chromatid exchanges occurring in these chromosomes are apparent as interchanges of brightly and dully fluorescing chromatids. A technique for detecting such exchanges by computer analysis of chromsome images has been developed and found to campare favorably with manual methods. The exchanges have been localized in the context of quinacrine banding patterns.


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