Abstract
A novel gene, prom-1, was isolated in a screen for Caenorhabditis elegans mutants with increased apoptosis in the germline. prom-1 encodes an F-box protein with limited homology to the putative human tumor suppressor FBXO47. Mutations in the prom-1 locus cause a strong reduction in bivalent formation, which results in increased embryonic lethality and a Him phenotype. Furthermore, retarded and asynchronous nuclear reorganization as well as reduced homologous synapsis occur during meiotic prophase. Accumulation of recombination protein RAD-51 in meiotic nuclei suggests disturbed repair of double-stranded DNA breaks. Nuclei in prom-1 mutant gonads timely complete mitotic proliferation and premeiotic replication, but they undergo prolonged delay upon meiotic entry. We, therefore, propose that prom-1 regulates the timely progression through meiotic prophase I and that in its absence the recognition of homologous chromosomes is strongly impaired.
Original language | English |
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Pages (from-to) | 4911-4920 |
Number of pages | 10 |
Journal | Molecular Biology of the Cell |
Volume | 18 |
Issue number | 12 |
DOIs | |
Publication status | Published - Dec 2007 |
Keywords
- CAENORHABDITIS-ELEGANS GERMLINE
- DAMAGE-INDUCED APOPTOSIS
- C-ELEGANS
- SYNAPTONEMAL COMPLEX
- NUCLEAR REORGANIZATION
- CHIASMA FORMATION
- CROSSING-OVER
- GENE FAMILY
- SYNAPSIS
- RECOMBINATION