
%0 Journal Article
%A Brero, A. 
%A Koehler, D. 
%A Cremer, T. 
%A Wolf, E. 
%A Zakhartchenko, V. 
%T 141 INDICATIONS FOR DNA DOUBLE-STRAND BREAK REPAIR IN EARLY BOVINE EMBRYOS
%J Reproduction, Fertility and Development
%D 2006/12/12
%V 19
%N 1
%P 188-188
%K 
%R https://doi.org/10.1071/RDV19N1AB141
%U https://www.publish.csiro.au/paper/RDV19N1AB141 
%X DNA double-strand breaks (DSBs) are considered the most severe type of DNA lesions, because such lesions, if unrepaired, lead to a loss of genome integrity. Soon after induction of DSBs, chromatin surrounding the damage is modified by phosphorylation of the histone variant H2AX, generating so-called &#947;H2AX, which is a hallmark of DSBs (Takahashi et al. 2005 Cancer Lett. 229, 171&#8211;179). &#947;H2AX appears to be a signal for the recruitment of proteins constituting the DNA repair machinery. Depending on the type of damage and the cell cycle stage of the affected cell, DSBs are repaired either by nonhomologous end joining or by homologous recombination using the sister chromatid DNA as template (Hoeijmakers 2001 Nature 411, 366&#8211;374). We used immunofluorescence to analyze chromatin composition during bovine development and found &#947;H2AX foci in both male and female pronuclei of IVF embryos. The number and size of foci varied considerably between embryos and between the male and female pronuclei. To test whether the observed &#947;H2AX foci represented sites of active DNA repair, we co-stained IVF zygotes for &#947;H2AX and 3 different proteins involved in homologous recombination repair of DSBs: NBS1 (phosphorylated at amino acid serine 343), 53BP1, and Rad51. We found co-localization of &#947;H2AX foci with phosphorylated NBS1 as well as with Rad51 but did not observe the presence of 53BP1 at &#947;H2AX foci in IVF zygotes. Our finding shows the presence of DSBs in IVF zygotes and suggests the capability of homologous recombination repair. The lack of 53BP1, a component of homologous recombination repair, which usually co-localizes with &#947;H2AX foci at exogenously induced DSBs (Schultz et al. 2000 J. Cell. Biol. 151, 1381&#8211;1390) poses the possibility that the mechanism present in early embryos differs substantially from that involved in DNA repair of DSBs in somatic cells. 
