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MORC Protein Family-related Signature Within Human Disease and Cancer

Overview
Journal Cell Death Dis
Date 2021 Nov 28
PMID 34839357
Citations 17
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Abstract

The microrchidia (MORC) family of proteins is a highly conserved nuclear protein superfamily, whose members contain common domain structures (GHKL-ATPase, CW-type zinc finger and coiled-coil domain) yet exhibit diverse biological functions. Despite the advancing research in previous decades, much of which focuses on their role as epigenetic regulators and in chromatin remodeling, relatively little is known about the role of MORCs in tumorigenesis and pathogenesis. MORCs were first identified as epigenetic regulators and chromatin remodelers in germ cell development. Currently, MORCs are regarded as disease genes that are involved in various human disorders and oncogenes in cancer progression and are expected to be the important biomarkers for diagnosis and treatment. A new paradigm of expanded MORC family function has raised questions regarding the regulation of MORCs and their biological role at the subcellular level. Here, we systematically review the progress of researching MORC members with respect to their domain architectures, diverse biological functions, and distribution characteristics and discuss the emerging roles of the aberrant expression or mutation of MORC family members in human disorders and cancer development. Furthermore, the illustration of related mechanisms of the MORC family has made MORCs promising targets for developing diagnostic tools and therapeutic treatments for human diseases, including cancers.

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References
1.
Inoue N, Hess K, Moreadith R, Richardson L, Handel M, Watson M . New gene family defined by MORC, a nuclear protein required for mouse spermatogenesis. Hum Mol Genet. 1999; 8(7):1201-7. DOI: 10.1093/hmg/8.7.1201. View

2.
Koch A, Kang H, Steinbrenner J, Dempsey D, Klessig D, Kogel K . MORC Proteins: Novel Players in Plant and Animal Health. Front Plant Sci. 2017; 8:1720. PMC: 5651269. DOI: 10.3389/fpls.2017.01720. View

3.
Perry J, Zhao Y . The CW domain, a structural module shared amongst vertebrates, vertebrate-infecting parasites and higher plants. Trends Biochem Sci. 2003; 28(11):576-80. DOI: 10.1016/j.tibs.2003.09.007. View

4.
Dong W, Vannozzi A, Chen F, Hu Y, Chen Z, Zhang L . MORC Domain Definition and Evolutionary Analysis of the MORC Gene Family in Green Plants. Genome Biol Evol. 2018; 10(7):1730-1744. PMC: 6048995. DOI: 10.1093/gbe/evy136. View

5.
Pan Z, Ding Q, Guo Q, Guo Y, Wu L, Wu L . MORC2, a novel oncogene, is upregulated in liver cancer and contributes to proliferation, metastasis and chemoresistance. Int J Oncol. 2018; 53(1):59-72. PMC: 5958890. DOI: 10.3892/ijo.2018.4333. View