Targeting Telomeres and Telomerase: Studies in Aging and Disease Utilizing CRISPR/Cas9 Technology

被引:13
作者
Brane, Andrew C. [1 ]
Tollefsbol, Trygve O. [1 ,2 ,3 ,4 ,5 ]
机构
[1] Univ Alabama Birmingham, Dept Biol, 1300 Univ Blvd, Birmingham, AL 35294 USA
[2] Univ Alabama Birmingham, Comprehens Ctr Hlth Aging, 1530 3rd Ave South, Birmingham, AL 35294 USA
[3] Univ Alabama Birmingham, Ctr Comprehens Canc, 1802 6th Ave South, Birmingham, AL 35294 USA
[4] Univ Alabama Birmingham, Nutr Obes Res Ctr, 1675 Univ Blvd, Birmingham, AL 35294 USA
[5] Univ Alabama Birmingham, Comprehens Diabet Ctr, 1825 Univ Blvd, Birmingham, AL 35294 USA
关键词
telomeres; telomerase; CRISPR; CRISPR/Cas9; Cas9; dCas9; cancer; aging; GENOMIC LOCI; STEM-CELLS; EXPRESSION; COMPONENTS; SEQUENCE;
D O I
10.3390/cells8020186
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Telomeres and telomerase provide a unique and important avenue of study in improving both life expectancy and quality of life due to their close association with aging and disease. While major advances in our understanding of these two biological mediators have characterized the last two decades, previous studies have been limited by the inability to affect change in real time within living cells. The last three years, however, have witnessed a huge step forward to overcome this limitation. The advent of the clustered regularly interspaced short palindromic repeats/CRISPR-associated (CRISPR/Cas) system has led to a wide array of targeted genetic studies that are already being employed to modify telomeres and telomerase, as well as the genes that affect them. In this review, we analyze studies utilizing the technology to target and modify telomeres, telomerase, and their closely associated genes. We also discuss how these studies can provide insight into the biology and mechanisms that underlie aging, cancer, and other diseases.
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页数:13
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