The polyubiquitin gene is essential for meiosis in fission yeast

K Okazaki, H Okayama, O Niwa - Experimental Cell Research, 2000 - Elsevier
K Okazaki, H Okayama, O Niwa
Experimental Cell Research, 2000Elsevier
We isolated a novel sporulation-deficient mutant of Schizosaccharomyces pombe. The
mutant did not have a mitotic growth defect but aborted meiosis at the first or the second
division with condensed chromosomes that failed to separate, abnormal spindle (s), and
disintegrated spindle pole bodies (SPBs). During the first division, the centromeres were
pulled to near the spindle poles but condensed divalent chromosomes remained at the
center. The failure to proceed to anaphase was also observed during a time-lapse recording …
We isolated a novel sporulation-deficient mutant of Schizosaccharomyces pombe. The mutant did not have a mitotic growth defect but aborted meiosis at the first or the second division with condensed chromosomes that failed to separate, abnormal spindle(s), and disintegrated spindle pole bodies (SPBs). During the first division, the centromeres were pulled to near the spindle poles but condensed divalent chromosomes remained at the center. The failure to proceed to anaphase was also observed during a time-lapse recording of a SPB protein tagged with green fluorescent protein. The polyubiquitin gene ubi4+, which encoded eight ubiquitins fused in tandem, complemented this mutant. The mutation, an A to G substitution, was identified within the ubi4+ gene at the A TG initiation codon. Disruption of the ubi4+ gene produced the same phenotypes. The ubi4+ mRNA was strongly induced for meiosis. However, ubiquitin increases only slightly, suggesting that the role of the polyubiquitin gene is to supply ubiquitin that is consumed by unidentified mechanisms. Before the ubi4 mutant cells entered meiosis, ubiquitin was greatly decreased indicating that shortage of ubiquitin caused abortion of meiosis. This work provides insights for the role of polyubiquitin gene and importance of ubiquitination in SPB integrity at the meiotic divisions.
Elsevier