The structural organization of cells of the Brc-1 mutant of the unicellular green algae Chlamydomonas reinhardtii grown in the light and in the dark has been studied. The Brc-1 mutant contains the brc-1 mutation in the nucleus gene LTS3. In the light, all membrane structures in mutant cells form normally and are well developed. In the dark under heterotrophic conditions, the mutant cells grew and divided well, however, all its cell membranes: plasmalemma, tonoplast, mitochondrial membranes, membranes of the nucleus shell and chloroplast, thylakoids, and the membranes of dictiosomes of the Golgi apparatus were not detected. In the dark under heterotrophic conditions, mutant cells well grow and divide. It were shown that a short-term (1-10 min) exposure of Brc-1 mutant cells to light leads to the restoration of all above-mentioned membrane structures. Possible reasons for the alterations of membrane structures are discussed.
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MicroPubl Biol
July 2024
Department of Genetic Engineering, Faculty of Biology-Oriented Science and Technology, Kindai University, Kinokawa, Wakayama, Japan.
Crossover designation factors such as COSA-1 are concentrated at the specific DNA double-strand break (DSB) sites to promote crossover formation. mutants, which show defects in the homologous chromosome pairing of chromosomes II and III, increase the COSA-1 foci/normal bivalent state compared to the expected value. The excess designation was suppressed by an additional mutation in in mutants.
View Article and Find Full Text PDFElife
August 2024
Institute of Molecular Biology, Department of Biology, University of Oregon, Eugene, United States.
The preservation of genome integrity during sperm and egg development is vital for reproductive success. During meiosis, the tumor suppressor BRCA1/BRC-1 and structural maintenance of chromosomes 5/6 (SMC-5/6) complex genetically interact to promote high fidelity DNA double strand break (DSB) repair, but the specific DSB repair outcomes these proteins regulate remain unknown. Using genetic and cytological methods to monitor resolution of DSBs with different repair partners in , we demonstrate that both BRC-1 and SMC-5 repress intersister crossover recombination events.
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June 2024
Biology Department, Texas Christian University, Fort Worth, Texas, United States.
Several strains of with mutations in or are readily available to aid in elucidating the functions of these two genes in DNA damage repair, meiosis, and gene repression. DW102 is the only strain to our knowledge with mutations in both and . However, several groups have reported the DW102 strain is indistinguishable from wild-type when observing levels of embryonic lethality, sensitivity to radiation, and rates of male progeny, while strains with mutations in either or display increased occurrence of these phenotypes.
View Article and Find Full Text PDFBiochim Biophys Acta Mol Cell Res
January 2024
Heinrich Heine University Düsseldorf, Medical Faculty, Institute of Toxicology, Moorenstraße 5, 40225 Düsseldorf, Germany. Electronic address:
The anticancer drug cisplatin (CisPt) injures post-mitotic neuronal cells, leading to neuropathy. Furthermore, CisPt triggers cell death in replicating cells. Here, we aim to unravel the relevance of different types of CisPt-induced DNA lesions for evoking neurotoxicity.
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July 2023
Biochemistry, Molecular, Cellular and Developmental Biology Graduate Group, Department of Molecular and Cellular Biology, University of California, Davis.
In mice, mutation of results in embryonic lethality, which is partially suppressed by mutation. In contrast, mutation of the BRCA1 ortholog, or its binding partner, , lead to only mild embryonic lethality. We show that in , and embryonic lethality is enhanced when ortholog, , is also mutated.
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