___

• Husi, H., Nmda receptors, neural pathways, and protein interaction databases, International Review of Neurobiology, 61, 49-77, (2004).
• Richards, A. L., Eckhardt, M. and Krogan, N. J., Mass spectrometry‐based protein–protein interaction networks for the study of human diseases, Molecular Systems Biology, 17, 1, (2021).
• Hsieh, Y.-Y. P., Makrantoni, V., Robertson, D., Marston, A. L. and Murray, A. W., Evolutionary repair: Changes in multiple functional modules allow meiotic cohesin to support mitosis, PLoS Biology, 18, 3, e3000635, (2020).
• Wenzel, E. S. and Singh, A. T. K., Cell-cycle checkpoints and aneuploidy on the path to cancer, In Vivo, 32, 1, 1-5, (2018).
• Marston, A. L., Shugoshins: Tension-sensitive pericentromeric adaptors safeguarding chromosome segregation, Molecular and Cellular Biology, 35, 4, 634-648, (2015).
• Kumar, R. and Agarwal, M., Shugoshin: From the perspective of clinical disorders, BioChem, 1, 2, 51-59, (2021).
• Yao, Y. and Dai, W., Shugoshins function as a guardian for chromosomal stability in nuclear division, Cell Cycle, 11, 14, 2631-2642, (2012).
• Hoevenaar, W. H. M. et al., Degree and site of chromosomal instability define its oncogenic potential, Nature Communications, 11, 1, (2020).
• Kovalchuk, I., Cancer and genomic instability in Genome stability, 495-519, (2021).
• Sugiyama, T. et al., Microsatellite frameshift variants in sgo1 of gastric cancer are not always associated with msi status, Journal of Clinical Pathology, (2020).
• Iwaizumi, M. et al., Human sgo1 downregulation leads to chromosomal instability in colorectal cancer, Gut, 58, 2, 249-260, (2009).
• Yamada, H. Y. et al., Haploinsufficiency of sgo1 results in deregulated centrosome dynamics, enhanced chromosomal instability and colon tumorigenesis, Cell Cycle, 11, 3, 479-488, (2012).
• Matsuura, S. et al., Sgol1 variant b induces abnormal mitosis and resistance to taxane in non-small cell lung cancers, Scientific Reports, 3, 1, (2013).
• Wang, L.-H., Yen, C.-J., Li, T.-N., Elowe, S., Wang, W.-C. and Wang, L. H.-C., Sgo1 is a potential therapeutic target for hepatocellular carcinoma, Oncotarget, 6, 4, 2023-2033, (2015).
• Faridi, R. et al., Mutations ofsgo2andcldn14collectively cause coincidental perrault syndrome, Clinical Genetics, 91, 2, 328-332, (2017).
• Domínguez-Ruiz, M. et al., Perrault syndrome with neurological features in a compound heterozygote for two twnk mutations: Overlap of twnk-related recessive disorders, Journal of Translational Medicine, 17, 1, (2019).
• Kennedy, S. R., Loeb, L. A. and Herr, A. J., Somatic mutations in aging, cancer and neurodegeneration, Mechanisms of Ageing and Development, 133, 4, 118-126, (2012).
• Chow, H.-M. and Herrup, K., Genomic integrity and the ageing brain, Nature Reviews Neuroscience, 16, 11, 672-684, (2015).
• Vijg, J., Dong, X., Milholland, B. and Zhang, L., Genome instability: A conserved mechanism of ageing?, Essays in Biochemistry, 61, 3, 305-315, (2017).
• Helbling-Leclerc, A., Garcin, C. and Rosselli, F., Beyond DNA repair and chromosome instability—fanconi anaemia as a cellular senescence-associated syndrome, Cell Death & Differentiation, 28, 4, 1159-1173, (2021).
• Iourov, I. Y., Vorsanova, S. G., Liehr, T., Kolotii, A. D. and Yurov, Y. B., Increased chromosome instability dramatically disrupts neural genome integrity and mediates cerebellar degeneration in the ataxia-telangiectasia brain, Human Molecular Genetics, 18, 14, 2656-2669, (2009).
• Iourov, I. Y., Yurov, Y. B., Vorsanova, S. G. and Kutsev, S. I., Chromosome instability, aging and brain diseases, Cells, 10, 5, 1256, (2021).
• Verzijlbergen, K. F. et al., Shugoshin biases chromosomes for biorientation through condensin recruitment to the pericentromere, eLife, 3, e01374-e01374, (2014).
• Nerusheva, O. O., Galander, S., Fernius, J., Kelly, D. and Marston, A. L., Tension-dependent removal of pericentromeric shugoshin is an indicator of sister chromosome biorientation, Genes and Development, 28, 12, 1291-1309, (2014).
• Smurova, K. and De Wulf, P., Centromere and pericentromere transcription: Roles and regulation ... In sickness and in health, Frontiers in Genetics, 9, 674, (2018).
• Duro, E. and Marston, A. L., From equator to pole: Splitting chromosomes in mitosis and meiosis, Genes and Development, 29, 2, 109-122, (2015).
• Fernius, J., Nerusheva, O. O., Galander, S., Alves, F. d. L., Rappsilber, J. and Marston, A. L., Cohesin-dependent association of scc2/4 with the centromere initiates pericentromeric cohesion establishment, Current Biology, 23, 7, 599-606, (2013).
• Uhlmann, F. and Nasmyth, K., Cohesion between sister chromatids must be established during DNA replication, Current Biology, 8, 20, 1095-1102, (1998).
• Ng, T. M., Waples, W. G., Lavoie, B. D. and Biggins, S., Pericentromeric sister chromatid cohesion promotes kinetochore biorientation, Molecular Biology of the Cell, 20, 3818-3827, (2009).
• Ribeiro, S. A. et al., Condensin regulates the stiffness of vertebrate centromeres, Molecular Biology of the Cell, 20, 9, 2371-2380, (2009).
• Stephens, A. D., Haase, J., Vicci, L., Taylor, R. M. and Bloom, K., Cohesin, condensin, and the intramolecular centromere loop together generate the mitotic chromatin spring, Journal of Cell Biology, 193, 7, 1167-1180, (2011).
• Stephens, A. D. et al., Pericentric chromatin loops function as a nonlinear spring in mitotic force balance, Journal of Cell Biology, 200, 6, 757-772, (2013).
• Yong-Gonzalez, V., Wang, B. D., Butylin, P., Ouspenski, I. and Strunnikov, A., Condensin function at centromere chromatin facilitates proper kinetochore tension and ensures correct mitotic segregation of sister chromatids, Genes to Cells, 12, 9, 1075-1090, (2007).
• Jaqaman, K. et al., Kinetochore alignment within the metaphase plate is regulated by centromere stiffness and microtubule depolymerases, Journal of Cell Biology, 188, 5, 665-679, (2010).
• Marston, A. L., Chromosome segregation in budding yeast: Sister chromatid cohesion and related mechanisms, Genetics, 196, 1, 31-63, (2014).
• Eshleman, H. D. and Morgan, D. O., Sgo1 recruits pp2a to chromosomes to ensure sister chromatid bi-orientation during mitosis, Journal of Cell Science, 2014, 127, 4974-4983, (2014).
• Peplowska, K., Wallek, A. U. and Storchova, Z., Sgo1 regulates both condensin and ipl1/aurora b to promote chromosome biorientation, PLOS Genetics, 10, 6, (2014).
• Rabitsch, K. P., Gregan, J., Schleiffer, A., Javerzat, J.-P., Eisenhaber, F. and Nasmyth, K., Two fission yeast homologs of drosophila mei-s332 are required for chromosome segregation during meiosis i and ii, Current Biology, 14, 4, 287-301, (2004).
• Tang, Z., Shu, H., Qi, W., Mahmood, N. A., Mumby, M. C. and Yu, H., Pp2a is required for centromeric localization of sgo1 and proper chromosome segregation, Developmental Cell, 10, 5, 575-585, (2006).
• Xu, Z., Cetin, B., Anger, M., Cho, U. S., Helmhart, W. and Xu, W., Structure and function of the pp2a-shugoshin interaction, Molecular Cell, 35, 4, 426-441, (2009).
• Kawashima, S. A., Yamagishi, Y., Honda, T., Lshiguro, K. I. and Watanabe, Y., Phosphorylation of h2a by bub1 prevents chromosomal instability through localizing shugoshin, Science, 327, 5962, 172-177, (2010).
• Yahya, G. et al., Phospho-regulation of the shugoshin - condensin interaction at the centromere in budding yeast, PLOS Genetics, 16, 8, e1008569, (2020).
• Indjeian, V. B., Stern, B. M. and Murray, A. W., The centromeric protein sgo1 is required to sense lack of tension on mitotic chromosomes, Science, 307, 5706, 130-133, (2005).
• Kim, T. et al., Kinetochores accelerate or delay apc/c activation by directing cdc20 to opposing fates, Genes and Development, 31, 11, 1089-1094, (2017).
• Levine, M. S. and Holland, A. J., The impact of mitotic errors on cell proliferation and tumorigenesis, Genes & Development, 32, 9-10, 620-638, (2018).
• Garcia-Gimenez, J. L., Garces, C., Roma-Mateo, C. and Pallardo, F. V., Oxidative stress-mediated alterations in histone post-translational modifications, Free Radical Biology and Medicine, 170, 6-18, (2021).
• Schmitz, M. L., Higgins, J. M. G. and Seibert, M., Priming chromatin for segregation: Functional roles of mitotic histone modifications, Cell Cycle, 19, 6, 625-641, (2020).
• Singh, D., Nishi, K., Khambata, K. and Balasinor, N. H., Introduction to epigenetics: Basic concepts and advancements in the field in Tollefsbol, T., Epigenetics and reproductive health, Elsevier, 25-44, United Kingdom, (2020).
• Ishiguro, T., Tanabe, K., Kobayashi, Y., Mizumoto, S., Kanai, M. and Kawashima, S. A., Malonylation of histone h2a at lysine 119 inhibits bub1-dependent h2a phosphorylation and chromosomal localization of shugoshin proteins, Scientific Reports, 8, 1, 1-10, (2018).
• Tyagi, M., Imam, N., Verma, K. and Patel, A. K., Chromatin remodelers: We are the drivers!!, Nucleus, 7, 4, 388-404, (2016).
• Min, S., Kim, K., Kim, S.-G., Cho, H. and Lee, Y., Chromatin-remodeling factor, rsf1, controls p53-mediated transcription in apoptosis upon DNA strand breaks, Cell Death & Disease, 9, 11, (2018).
• Lee, H.-S. et al., The chromatin remodeler rsf1 controls centromeric histone modifications to coordinate chromosome segregation, Nature Communications, 9, 1, 3848-3848, (2018).
• Cai, G., Yang, Q. and Sun, W., Rsf1 in cancer: Interactions and functions, Cancer Cell International, 21, 1, (2021).
• Hargreaves, D. C. and Crabtree, G. R., Atp-dependent chromatin remodeling: Genetics, genomics and mechanisms, Cell Research, 21, 3, 396-420, (2011).
• Hormozdiari, F. et al., The effect of insertions and deletions on wirings in protein-protein interaction networks: A large-scale study, Journal of Computational Biology, 16, 2, 159-167, (2009).
• Wang, X., Gene mutation‐based and specific therapies in precision medicine, Journal of Cellular and Molecular Medicine, 20, 4, 577-580, (2016).