Introduction
Analysis of the XRCC genes has played an
important part in understanding mammalian DNA repair processes,
especially those involved in double-strand break (DSB) repair.
Most of these genes were identified through their ability to
correct DNA damage hypersensitivity in rodent cell lines, and
they represent components of several different repair pathways
including base-excision repair, non-homologous end joining, and
homologous recombination. We document the phenotypic effects of
mutation of the XRCC genes, and the current state of our
knowledge of their functions. In addition to their continuing
importance in discovering mechanisms of DNA repair, analysis of
the XRCC genes is making a substantial contribution to the
understanding of specific human disorders, including cancer.
PMID: 12767346
Expression
XRCC1 is involved in DNA strand-break repair,
homologous recombination, and sister chromatid exchange and is
expressed as a low-abundance mRNA with elevated expression in
testis.
PMID: 8862781
Normal young adult male testis and enriched
populations of pachytene spermatocytes and round spermatids
displayed significantly higher levels of Xrcc-1 expression than
other mouse tissues, although Xrcc-1 transcripts were found in
low abundance in all tested tissues. Cultured mouse cell lines
displayed levels of expression similar to male germ cells, which
is a striking contrast to the levels of expression obtained in
somatic tissues from the mouse. The relatively high levels of
expression identified in male germ cells indicate Xrcc-1 may
have an important role in male germ cell physiology.
PMID: 7892645
These data and the high levels of XRCC1
protein detected in testis indicate that XRCC1 may play an
important role in DNA processing during meiogenesis and
recombination in germ cells.
PMID: 1353960