Consequences of genetic variants in miRNA genes

被引:16
|
作者
Machowska, Magdalena [1 ]
Galka-Marciniak, Paulina [1 ]
Kozlowski, Piotr [1 ]
机构
[1] Polish Acad Sci, Inst Bioorgan Chem, Dept Mol Genet, Noskowskiego 12-14, PL-61704 Poznan, Poland
关键词
miR-142 in AML; miR-96 in hearing loss; miR-184 in keratoconus; miR-204 in retinal dystrophy; miR-15; miR-16 in CLL; miR140 in skeletal dysplasia; SINGLE-NUCLEOTIDE POLYMORPHISM; MICRORNA EXPRESSION; LET-7; FAMILY; HEARING-LOSS; SEED REGION; FUNCTIONAL POLYMORPHISM; CERVICAL-CANCER; DOWN-REGULATION; COPY NUMBER; RISK;
D O I
10.1016/j.csbj.2022.11.036
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
MicroRNAs (miRNAs) are small non-coding RNAs that posttranscriptionally regulate the expression of most genes. They are involved in regulating many physiological processes, and aberrations in the levels of different miRNAs play an important role in the development of many diseases, including autoimmune diseases, neuropsychiatric diseases, and cancers. Although miRNAs are being intensively studied and levels of many miRNAs are either specifically increased or decreased in particular diseases, very little is known about the genetic variations of miRNA genes and their impact on the functioning of miRNA genes and human diseases. To shed more light on the potential effects of genetic variants in miRNA genes, we review here representative examples of SNPs, mutations linked to Mendelian diseases, and cancer somatic mutations located in miRNA genes and discuss their potential effects on the expression of miRNA genes, i.e., the structure and processing of miRNA precursors, the levels of generated miRNAs, miRNA target recognition/silencing, and impact on human diseases.CO 2022 The Authors. Published by Elsevier B.V. on behalf of Research Network of Computational and Structural Biotechnology. This is an open access article under the CC BY-NC-ND license (http://creative-commons.org/licenses/by-nc-nd/4.0/).
引用
收藏
页码:6443 / 6457
页数:15
相关论文
共 50 条
  • [41] Genetic variants for head size share genes and pathways with cancer
    Knol, Maria J.
    Poot, Raymond A.
    Evans, Tavia E.
    Satizabal, Claudia L.
    Mishra, Aniket
    Sargurupremraj, Muralidharan
    van der Auwera, Sandra
    Duperron, Marie-Gabrielle
    Jian, Xueqiu
    Hostettler, Isabel C.
    Van Dam-Nolen, Dianne H. K.
    Lamballais, Sander
    Pawlak, Mikolaj A.
    Lewis, Cora E.
    Carrion-Castillo, Amaia
    van Erp, Theo G. M.
    Reinbold, Celine S.
    Shin, Jean
    Scholz, Markus
    Haberg, Asta K.
    Kampe, Anders
    Li, Gloria H. Y.
    Avinun, Reut
    Atkins, Joshua R.
    Hsu, Fang-Chi
    Amod, Alyssa R.
    Lam, Max
    Tsuchida, Ami
    Teunissen, Mariel W. A.
    Aygun, Nil
    Patel, Yash
    Liang, Dan
    Beiser, Alexa S.
    Beyer, Frauke
    Bis, Joshua C.
    Bos, Daniel
    Bryan, R. Nick
    Buelow, Robin
    Caspers, Svenja
    Catheline, Gwenaelle
    Cecil, Charlotte A. M.
    Dalvie, Shareefa
    Dartigues, Jean-Francois
    DeCarli, Charles
    Enlund-Cerullo, Maria
    Ford, Judith M.
    Franke, Barbara
    Freedman, Barry, I
    Friedrich, Nele
    Green, Melissa J.
    CELL REPORTS MEDICINE, 2024, 5 (05)
  • [42] Genetic variants of membrane metallopeptidase genes in inflammatory bowel diseases
    Tavano, Francesca
    Palmieri, Orazio
    di Mola, Fabio Francesco
    Latiano, Anna
    Burbaci, Francesca Paola
    Valvano, Maria Rosa
    Corritore, Giuseppe
    Augello, Bartolomeo
    Merla, Giuseppe
    Annese, Vito
    Andriulli, Angelo
    di Sebastiano, Pierluigi
    DIGESTIVE AND LIVER DISEASE, 2013, 45 (12) : 1003 - 1010
  • [43] Genetic variants in splicing factor genes and susceptibility to bladder cancer
    Wang, Xi
    Guo, Zheng
    Zhu, Huanhuan
    Xin, Junyi
    Yuan, Lin
    Qin, Chao
    Wang, Meilin
    Zhang, Zhengdong
    Wang, Yunyan
    Chu, Haiyan
    GENE, 2022, 809
  • [44] Genetic factors and insulin secretion -: Gene variants in the IGF genes
    t Hart, LM
    Fritsche, A
    Rietveld, I
    Dekker, JM
    Nijpels, G
    Machicao, F
    Stumvoll, M
    van Duijn, CM
    Häring, HU
    Heine, RJ
    Maassen, JA
    van Haeften, TW
    DIABETES, 2004, 53 : S26 - S30
  • [45] Genetic variants in telomere pathways genes and breast cancer risk
    Shen, Jing
    Gammon, Marilie
    Wu, Hui-Chen
    Terry, Mary Beth
    Wang, Qiao
    Bradshaw, Patrick
    Teitelbaum, Susan
    Neugut, Alfred
    Santella, Regina
    CANCER RESEARCH, 2009, 69
  • [46] Genetic variants in inflammation pathway genes and asthma in glioma susceptibility
    Amirian, E.
    Liu, Yanhong
    Scheurer, Michael E.
    El-Zein, Randa
    Gilbert, Mark R.
    Bondy, Melissa L.
    NEURO-ONCOLOGY, 2010, 12 (05) : 444 - 452
  • [47] Rare genetic variants in genes of NO metabolism in lacunar stroke patients
    Loos, C. M. J.
    Staals, J.
    Smeets, H. J. M.
    van Oostenbrugge, R. J.
    CEREBROVASCULAR DISEASES, 2013, 35 : 39 - 39
  • [48] Causal Inference of Genetic Variants and Genes in Amyotrophic Lateral Sclerosis
    Pan, Siyu
    Liu, Xinxuan
    Liu, Tianzi
    Zhao, Zhongming
    Dai, Yulin
    Wang, Yin-Ying
    Jia, Peilin
    Liu, Fan
    FRONTIERS IN GENETICS, 2022, 13
  • [49] Novel genetic variants in microRNA genes and familial breast cancer
    Shen, Jie
    Ambrosone, Christine B.
    Zhao, Hua
    INTERNATIONAL JOURNAL OF CANCER, 2009, 124 (05) : 1178 - 1182
  • [50] Knowledge Base on Diabetes-Related Genes and Genetic Variants
    Thareja, Gaurav
    John, Sumi E.
    Alsmadi, Osama
    Thangavel, Alphonse T.
    DIABETES, 2012, 61 : A676 - A676