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Title: Induction and repair of chromosome aberrations in scid cells measured by premature chromosome condensation

Journal Article · · Radiation Research
DOI:https://doi.org/10.2307/3579193· OSTI ID:478296
; ;  [1];  [2]
  1. Stanford Univ. School of Medicine, CA (United States)
  2. Chinese Academy of Medical Sciences, Beijing (China)

Severe combined immunodeficient (scid) murine cells, which are defective in both repair of DNA double-strand breaks and V(D)J recombination, are deficient in DNA-dependent protein kinase (DNA-PK), a protein which forms an activated complex with the DNA end-binding Ku proteins (p80 and p70) upon association with damaged DNA. Xrs 5 cells are deficient in the Ku p80 protein and also fail to form an active DNA-PK repair complex. Since both scid and xrs cells are defective in the same protein complex, we compared the kinetics of chromosome repair in scid cells to results published previously for xrs 5 cells. C.B-17 cells, scid cells and scid cells complemented with a single human chromosome 8 were irradiated with 6 Gy and allowed to repair from 0-24 h before fusion to HeLa cells for chromosome condensation. Breaks and dicentrics were visualized by fluorescence in situ hybridization. All cells had the same initial amount of chromosome damage, but scid cells had a slower rate of rejoining, more unrejoined breaks and more dicentrics than C.B-17 and scid cells with human chromosome 8. The scid cells appear to respond differently than xrs 5 cells, despite both cells lacking an essential component of the same DNA repair complex. 40 refs., 6 figs., 3 tabs.

Sponsoring Organization:
USDOE
OSTI ID:
478296
Journal Information:
Radiation Research, Vol. 145, Issue 1; Other Information: PBD: Jan 1996
Country of Publication:
United States
Language:
English