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DOI 10.1007/s00005-017-0470-x

Медицинская библиотека · Archivum immunologiae et therapiae experimentalis · 2017

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

Chou Chon-Kit, Tang Chin-Ju, Chou Han-Lin, Liu Chun-Yen, Ng Ming-Chong, Chang Yu-Ting, Yuan Shyng-Shiou F, Tsai Eing-Mei, Chiu Chien-Chih

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Аннотация

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.

Для цитирования: Chou Chon-Kit, Tang Chin-Ju, Chou Han-Lin, Liu Chun-Yen, Ng Ming-Chong, Chang Yu-Ting, Yuan Shyng-Shiou F, Tsai Eing-Mei, Chiu Chien-Chih. The Potential Role of Krüppel-Like Zinc-Finger Protein Glis3 in Genetic Diseases and Cancers.. Archivum immunologiae et therapiae experimentalis. 2017. DOI: 10.1007/s00005-017-0470-x.

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