Caenorhabditis elegans NSE3 homolog (MAGE-1) is involved in genome stability and acts in inter-sister recombination during meiosis

Author:

Odiba Arome Solomon12,Liao Guiyan1,Ezechukwu Chiemekam Samuel1,Zhang Lanlan13,Hong Ye4,Fang Wenxia1,Jin Cheng12,Gartner Anton5,Wang Bin1

Affiliation:

1. State Key Laboratory of Non-food Biomass and Enzyme Technology, Guangxi Academy of Sciences , Nanning 530007 , China

2. State Key Laboratory of Mycology, Institute of Microbiology, Chinese Academy of Sciences , Beijing 100101 , China

3. College of Life Sciences, Hebei University , Baoding 071002 , China

4. Shandong Provincial Key Laboratory of Animal Cell and Developmental Biology, School of Life Sciences, Shandong University , Qingdao 266237 , China

5. IBS Center for Genomic Integrity, Department for Biological Sciences, Ulsan National Institute of Science and Technology , Ulsan 689-798 , Republic of Korea

Abstract

Abstract Melanoma antigen (MAGE) genes encode for a family of proteins that share a common MAGE homology domain. These genes are conserved in eukaryotes and have been linked to a variety of cellular and developmental processes including ubiquitination and oncogenesis in cancer. Current knowledge on the MAGE family of proteins mainly comes from the analysis of yeast and human cell lines, and their functions have not been reported at an organismal level in animals. Caenorhabditis elegans only encodes 1 known MAGE gene member, mage-1 (NSE3 in yeast), forming part of the SMC-5/6 complex. Here, we characterize the role of mage-1/nse-3 in mitosis and meiosis in C. elegans. mage-1/nse-3 has a role in inter-sister recombination repair during meiotic recombination and for preserving chromosomal integrity upon treatment with a variety of DNA-damaging agents. MAGE-1 directly interacts with NSE-1 and NSE-4. In contrast to smc-5, smc-6, and nse-4 mutants which cause the loss of NSE-1 nuclear localization and strong cytoplasmic accumulation, mage-1/nse-3 mutants have a reduced level of NSE-1::GFP, remnant NSE-1::GFP being partially nuclear but largely cytoplasmic. Our data suggest that MAGE-1 is essential for NSE-1 stability and the proper functioning of the SMC-5/6 complex.

Funder

National Natural Science Foundation of China

Guangxi Natural Science foundation

Guangxi Academy of Sciences

Korean Institute for Basic Science

Shandong University Qilu Young Scholars

Office of Research Infrastructure Programs, National Institutes of Health

Publisher

Oxford University Press (OUP)

Subject

Genetics

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