The Potential Role of Krüppel-Like Zinc-Finger Protein Glis3 in Genetic Diseases and Cancers

被引:0
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作者
Chon-Kit Chou
Chin-Ju Tang
Han-Lin Chou
Chun-Yen Liu
Ming-Chong Ng
Yu-Ting Chang
Shyng-Shiou F. Yuan
Eing-Mei Tsai
Chien-Chih Chiu
机构
[1] Kaohsiung Medical University,Graduate Institute of Natural Products
[2] Kaohsiung Medical University,Department of Biotechnology
[3] National Sun Yat-sen University,Department of Biological Sciences
[4] Kaohsiung Medical University Hospital,Translational Research Center and Department of Medical Research
[5] Kaohsiung Medical University,Research Center for Environment Medicine
[6] Kaohsiung Medical University,undefined
关键词
Glis3; Diabetes mellitus; Cys2/His2 zinc-finger domains; Congenital hypothyroidism; Polycystic kidney disease; Cancer;
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摘要
Gli-similar 3 (Glis3) belongs to a Glis subfamily of Krüppel-like zinc-finger transcription factors characterized to regulate a set of downstream targets essential for cellular functions, including pancreatic development, β-cell maturation and maintenance, and insulin production. Examination of the DNA-binding domain of Glis3 reveals that this domain contains a repeated cysteine 2/histidine 2 (Cys2/His2) zinc-finger motif in the central region where the recognized DNA sequence binds. The loss of the production of pancreatic hormones, such as insulin 1 and 2, is linked to the down-regulation of β cells-related genes and promotes the apoptotic death of β cells found in mutant Glis3. Although accumulating studies converge on the Glis3 functioning in β cells, recently, there have been developments in the field of Glis3 using knockdown/mutant mice to better understand the role of Glis3 in diseases. The Glis3 mutant mice have been characterized for their propensity to develop congenital hypothyroidism, polycystic kidney disease, and some types of cancer. In this review, we attempt to comprehensively summarize the knowledge of Glis3, including its structure and general function in cells. We also collected and organized the academic achievements related to the possible mechanisms of Glis3-related diseases.
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页码:381 / 389
页数:8
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