Mosaic loss of the Y chromosome in human neurodegenerative and oncological diseases
The development of new biomarkers for prediction and early detection of human diseases, as well as for monitoring the response to therapy is one of the most relevant areas of modern human genetics and genomics. Until recently, it was believed that the function of human Y chromosome genes was limited...
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Siberian Branch of the Russian Academy of Sciences, Federal Research Center Institute of Cytology and Genetics, The Vavilov Society of Geneticists and Breeders
2023-09-01
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Series: | Вавиловский журнал генетики и селекции |
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Online Access: | https://vavilov.elpub.ru/jour/article/view/3867 |
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author | I. L. Kuznetsova L. I. Uralsky T. V. Tyazhelova T. V. Andreeva E. I. Rogaev |
author_facet | I. L. Kuznetsova L. I. Uralsky T. V. Tyazhelova T. V. Andreeva E. I. Rogaev |
author_sort | I. L. Kuznetsova |
collection | DOAJ |
description | The development of new biomarkers for prediction and early detection of human diseases, as well as for monitoring the response to therapy is one of the most relevant areas of modern human genetics and genomics. Until recently, it was believed that the function of human Y chromosome genes was limited to determining sex and controlling spermatogenesis. Thanks to occurance of large databases of the genome-wide association study (GWAS), there has been a transition to the use of large samples for analyzing genetic changes in both normal and pathological conditions. This has made it possible to assess the association of mosaic aneuploidy of the Y chromosome in somatic cells with a shorter lifespan in men compared to women. Based on data from the UK Biobank, an association was found between mosaic loss of the Y chromosome (mLOY) in peripheral blood leukocytes and the age of men over 70, as well as a number of oncological, cardiac, metabolic, neurodegenerative, and psychiatric diseases. As a result, mLOY in peripheral blood cells has been considered a potential marker of biological age in men and as a marker of certain age-related diseases. Currently, numerous associations have been identified between mLOY and genes based on GWAS and transcriptomes in affected tissues. However, the exact cause of mLOY and the impact and consequences of this phenomenon at the whole organism level have not been established. In particular, it is unclear whether aneuploidy of the Y chromosome in blood cells may affect the development of pathologies that manifest in other organs, such as the brain in Alzheimer’s disease, or whether it is a neutral biomarker of general genomic instability. This review examines the main pathologies and genetic factors associated with mLOY, as well as the hypotheses regarding their interplay. Special attention is given to recent studies on mLOY in brain cells in Alzheimer’s disease. |
format | Article |
id | doaj-art-0d81f4d8546543ec88a61d4d84988cab |
institution | Kabale University |
issn | 2500-3259 |
language | English |
publishDate | 2023-09-01 |
publisher | Siberian Branch of the Russian Academy of Sciences, Federal Research Center Institute of Cytology and Genetics, The Vavilov Society of Geneticists and Breeders |
record_format | Article |
series | Вавиловский журнал генетики и селекции |
spelling | doaj-art-0d81f4d8546543ec88a61d4d84988cab2025-02-01T09:58:12ZengSiberian Branch of the Russian Academy of Sciences, Federal Research Center Institute of Cytology and Genetics, The Vavilov Society of Geneticists and BreedersВавиловский журнал генетики и селекции2500-32592023-09-0127550251110.18699/VJGB-23-611380Mosaic loss of the Y chromosome in human neurodegenerative and oncological diseasesI. L. Kuznetsova0L. I. Uralsky1T. V. Tyazhelova2T. V. Andreeva3E. I. Rogaev4Vavilov Institute of General Genetics, Russian Academy of Sciences, Department of Genomics and Human Genetics; Sirius University of Science and Technology, Scientific Center for Genetics and Life SciencesVavilov Institute of General Genetics, Russian Academy of Sciences, Department of Genomics and Human Genetics; Sirius University of Science and Technology, Scientific Center for Genetics and Life SciencesVavilov Institute of General Genetics, Russian Academy of Sciences, Department of Genomics and Human GeneticsVavilov Institute of General Genetics, Russian Academy of Sciences, Department of Genomics and Human Genetics; Sirius University of Science and Technology, Scientific Center for Genetics and Life Sciences Lomonosov Moscow State University, Center for Genetics and Genetic Technologies, Faculty of BiologyVavilov Institute of General Genetics, Russian Academy of Sciences, Department of Genomics and Human Genetics; Sirius University of Science and Technology, Scientific Center for Genetics and Life Sciences Lomonosov Moscow State University, Center for Genetics and Genetic Technologies, Faculty of BiologyThe development of new biomarkers for prediction and early detection of human diseases, as well as for monitoring the response to therapy is one of the most relevant areas of modern human genetics and genomics. Until recently, it was believed that the function of human Y chromosome genes was limited to determining sex and controlling spermatogenesis. Thanks to occurance of large databases of the genome-wide association study (GWAS), there has been a transition to the use of large samples for analyzing genetic changes in both normal and pathological conditions. This has made it possible to assess the association of mosaic aneuploidy of the Y chromosome in somatic cells with a shorter lifespan in men compared to women. Based on data from the UK Biobank, an association was found between mosaic loss of the Y chromosome (mLOY) in peripheral blood leukocytes and the age of men over 70, as well as a number of oncological, cardiac, metabolic, neurodegenerative, and psychiatric diseases. As a result, mLOY in peripheral blood cells has been considered a potential marker of biological age in men and as a marker of certain age-related diseases. Currently, numerous associations have been identified between mLOY and genes based on GWAS and transcriptomes in affected tissues. However, the exact cause of mLOY and the impact and consequences of this phenomenon at the whole organism level have not been established. In particular, it is unclear whether aneuploidy of the Y chromosome in blood cells may affect the development of pathologies that manifest in other organs, such as the brain in Alzheimer’s disease, or whether it is a neutral biomarker of general genomic instability. This review examines the main pathologies and genetic factors associated with mLOY, as well as the hypotheses regarding their interplay. Special attention is given to recent studies on mLOY in brain cells in Alzheimer’s disease.https://vavilov.elpub.ru/jour/article/view/3867mosaic loss of y chromosome (mloy)alzheimer’s diseasegwasage-related diseasesoncological diseases |
spellingShingle | I. L. Kuznetsova L. I. Uralsky T. V. Tyazhelova T. V. Andreeva E. I. Rogaev Mosaic loss of the Y chromosome in human neurodegenerative and oncological diseases Вавиловский журнал генетики и селекции mosaic loss of y chromosome (mloy) alzheimer’s disease gwas age-related diseases oncological diseases |
title | Mosaic loss of the Y chromosome in human neurodegenerative and oncological diseases |
title_full | Mosaic loss of the Y chromosome in human neurodegenerative and oncological diseases |
title_fullStr | Mosaic loss of the Y chromosome in human neurodegenerative and oncological diseases |
title_full_unstemmed | Mosaic loss of the Y chromosome in human neurodegenerative and oncological diseases |
title_short | Mosaic loss of the Y chromosome in human neurodegenerative and oncological diseases |
title_sort | mosaic loss of the y chromosome in human neurodegenerative and oncological diseases |
topic | mosaic loss of y chromosome (mloy) alzheimer’s disease gwas age-related diseases oncological diseases |
url | https://vavilov.elpub.ru/jour/article/view/3867 |
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