| Summary: | During sexual reproduction/conjugation of the ciliate <i>Tetrahymena thermophila</i>, the germinal micronucleus undergoes meiosis resulting in four haploid micronuclei (hMICs). All hMICs undergo post-meiotic DNA double-strand break (PM-DSB) formation, cleaving their genome. DNA lesions are subsequently repaired in only one ‘selected’ hMIC, which eventually produces gametic pronuclei. DNA repair in the selected hMIC involves chromatin remodeling by switching from the heterochromatic to the euchromatic state of its genome. Here, we demonstrate that, among the 15 <i>Tetrahymena</i> Snf2 family proteins, a core of the ATP-dependent chromatin remodeling complex in <i>Tetrahymena</i>, the germline nucleus specific Iswi in <i>Tetrahymena</i> IswiG<sup>Tt</sup> and Rad5<sup>Tt</sup> is crucial for the generation of gametic pronuclei. In either gene knockout, the selected hMIC which shows euchromatin markers such as lysine-acetylated histone H3 does not appear, but all hMICs in which markers for DNA lesions persist are degraded, indicating that both IswiG<sup>Tt</sup> and Rad5<sup>Tt</sup> have important roles in repairing PM-DSB DNA lesions and remodeling chromatin for the euchromatic state in the selected hMIC.
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