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  1. NTU Theses and Dissertations Repository
  2. 醫學院
  3. 分子醫學研究所
請用此 Handle URI 來引用此文件: http://tdr.lib.ntu.edu.tw/jspui/handle/123456789/78531
完整後設資料紀錄
DC 欄位值語言
dc.contributor.advisor張以承(Yi-Cheng Chang)
dc.contributor.authorTsui-Wei Chyanen
dc.contributor.author錢翠微zh_TW
dc.date.accessioned2021-07-11T15:02:20Z-
dc.date.available2021-08-29
dc.date.copyright2019-08-29
dc.date.issued2019
dc.date.submitted2019-08-19
dc.identifier.citation1. Kharitonenkov, A. and A.C. Adams, Inventing new medicines: The FGF21 story. Molecular Metabolism, 2014. 3(3): p. 221-229.
2. Itoh, N., Hormone-like (endocrine) Fgfs: their evolutionary history and roles in development, metabolism, and disease. Cell and tissue research, 2010. 342(1): p. 1-11.
3. Angelin, B., Tobias E. Larsson, and M. Rudling, Circulating Fibroblast Growth Factors as Metabolic Regulators—A Critical Appraisal. Cell Metabolism, 2012. 16(6): p. 693-705.
4. Degirolamo, C., C. Sabba, and A. Moschetta, Therapeutic potential of the endocrine fibroblast growth factors FGF19, FGF21 and FGF23. Nat Rev Drug Discov, 2016. 15(1): p. 51-69.
5. Badman, M.K., et al., Hepatic fibroblast growth factor 21 is regulated by PPARalpha and is a key mediator of hepatic lipid metabolism in ketotic states. Cell Metab, 2007. 5(6): p. 426-37.
6. Xu, J., et al., Fibroblast growth factor 21 reverses hepatic steatosis, increases energy expenditure, and improves insulin sensitivity in diet-induced obese mice. Diabetes, 2009. 58(1): p. 250-9.
7. Fisher, f.M., et al., Obesity Is a Fibroblast Growth Factor 21 (FGF21)-Resistant State. Diabetes, 2010. 59(11): p. 2781.
8. Li, H., et al., Fibroblast growth factor 21 increases insulin sensitivity through specific expansion of subcutaneous fat. Nature Communications, 2018. 9(1): p. 272.
9. Emanuelli, B., et al., Interplay between FGF21 and insulin action in the liver regulates metabolism. The Journal of Clinical Investigation, 2014. 124(2): p. 515-527.
10. Owen, Bryn M., et al., FGF21 Acts Centrally to Induce Sympathetic Nerve Activity, Energy Expenditure, and Weight Loss. Cell Metabolism, 2014. 20(4): p. 670-677.
11. Domouzoglou, E.M., et al., Fibroblast growth factors in cardiovascular disease: The emerging role of FGF21. American journal of physiology. Heart and circulatory physiology, 2015. 309(6): p. H1029-H1038.
12. Planavila, A., et al., Fibroblast growth factor 21 protects against cardiac hypertrophy in mice. Nature Communications, 2013. 4: p. 2019.
13. Gunster, M.J., et al., Identification and characterization of interactions between the vertebrate polycomb-group protein BMI1 and human homologs of polyhomeotic. Molecular and Cellular Biology, 1997. 17(4): p. 2326.
14. Thiesen, H.J., Multiple genes encoding zinc finger domains are expressed in human T cells. New Biol, 1990. 2(4): p. 363-74.
15. Zhang, D., et al., Arginine and glutamate-rich 1 (ARGLU1) interacts with mediator subunit 1 (MED1) and is required for estrogen receptor-mediated gene transcription and breast cancer cell growth. The Journal of biological chemistry, 2011. 286(20): p. 17746-17754.
16. Sigurdsson, S., et al., Sequence variants in ARHGAP15, COLQ and FAM155A associate with diverticular disease and diverticulitis. Nature Communications, 2017. 8: p. 15789.
17. Dehghan, A., et al., Meta-analysis of genome-wide association studies in >80 000 subjects identifies multiple loci for C-reactive protein levels. Circulation, 2011. 123(7): p. 731-8.
18. Derks, E.M., A.H. Zwinderman, and E.R. Gamazon, The Relation Between Inflation in Type-I and Type-II Error Rate and Population Divergence in Genome-Wide Association Analysis of Multi-Ethnic Populations. Behavior Genetics, 2017. 47(3): p. 360-368.
19. Allard, D., et al., Novel mutations of the PCSK9 gene cause variable phenotype of autosomal dominant hypercholesterolemia. Hum Mutat, 2005. 26(5): p. 497.
dc.identifier.urihttp://tdr.lib.ntu.edu.tw/jspui/handle/123456789/78531-
dc.description.abstract纖維母細胞生長因子(FGF)最早是在從腦下垂體的萃取物中發現的。到目前為止發現FGF家族有22個成員,其中大部分屬於自分泌(autocrine)或旁分泌(paracrine),然而FGF-19、21和23,其訊息傳遞的方式是透過血液循環到達特定的組織器官與典型的FGFs不同,被歸類為新興的“賀爾蒙”(endocrine hormone)。
FGF-21施打於糖尿病動物可以降低血糖, 減少脂肪肝, 並減輕體重,而過度表現FGF-21於小鼠可以抵抗高脂飲食產生的肥胖,並且增加棕色脂肪組織與能量消耗, 這些證據, 強烈顯示FGF-21為重要的新興代謝荷爾蒙, 可調控糖份與脂質的代謝,為重要之藥物標的。然而調控FGF-21的基因位點迄今尚未知。
本實驗檢體來源為台灣人體生物資料庫5000人之血清檢體,利用ELISA的方法測定FGF-21濃度。與台灣人體生物資料庫所提供的全基因組SNP基因型定型,利用PLINK軟體分析,尋找與FGF-21濃度相關之基因位點。我們除去糖尿病患者(n=607)後,分析4393名非糖尿病受試者, 並校正年齡、性別、BMI。
以P<10-6為閾值找到5個SNP位點與血清FGF-21濃度相關,這些位點都在內含子或兩基因位點之間,無位點在外顯子。這些SNP分別位於或是鄰近於Polyhomeotic Homolog 2(PHC2)、Zinc Finger And SCAN Domain Containing 20(ZSCAN20)、Arginine And Glutamate Rich 1( ARGLU1)、Family With Sequence Similarity 155 Member A(FAM155A)、Regulator Of G Protein Signaling 6(RGS6) 。這些基因參與基因的調節轉錄與細胞訊息傳遞,意味著這些基因可能調節FGF-21血清濃度機轉。
zh_TW
dc.description.abstractFibroblast growth factor (FGF) was first found in extracts from the pituitary gland. Up to date, the FGF family has 22 members, most of which act in autocrine or paracrine fashion. However, unlike typical FGFs, FGF-19, 21 and 23, whose message transmission is through the blood circulation to reach specific tissues and organs, are classified as novel endocrine hormone.
Administration of FGF-21 lowers blood glucose, reduces fatty liver, and results in weight loss. Forced expression of FGF-21 in mice resists obesity caused by high-fat diet and increases brown adipose tissue and energy expenditure. These evidences strongly suggest that FGF-21 is an important new hormone that regulates the metabolism of glucose and lipids, and is an important drug target. However, the genetic loci regulating serum FGF-21 level is unknown.
We recruited 5,000 participants from the Taiwan Biobank and the levels of FGF-21 of these participants were determined using ELISA. Genome-wide SNP genotyping of FGF-21 provided by Taiwan Biobank database was analyzed using pLINK software to locate genetic loci associated with circulating FGF-21 levels. After removing diabetic patients (n=607), 4393 non-diabetic subjects were analyzed and the analyses were further adjusted by age, gender, BMI.
Five SNPs loci were associated with serum FGF-21 levels using P<10-6 as threshold. These SNPs are within introns or are between two gene loci and none are found to be located within exons. These associated SNPs are located at or adjacent to the Polyhomeotic Homolog 2(PHC2)、Zinc Finger And SCAN Domain Containing 20(ZSCAN20)、Arginine And Glutamate Rich 1( ARGLU1)、Family With Sequence Similarity 155 Member A(FAM155A)、Regulator Of G Protein Signaling 6(RGS6). These genes are involved in the regulation of gene transcription and cell signal transduction. This means these genes may be involved in the regulation of the serum concentration of FGF-21
en
dc.description.provenanceMade available in DSpace on 2021-07-11T15:02:20Z (GMT). No. of bitstreams: 1
ntu-108-P06448002-1.pdf: 1865211 bytes, checksum: eb1e7924013a68217efda1d8f8e75c7f (MD5)
Previous issue date: 2019
en
dc.description.tableofcontents口試委員會審定書 i
誌謝 ii
中文摘要 iii
英文摘要 iv
第一章研究背景與動機 3
1. FGF21為新興內分泌賀爾蒙 3
2. FGF21調節全身代謝調節劑 6
3. 研究目的 8
第二章 研究方法 9
1. 研究架構 9
2. 實驗對象 9
3. FGF21濃度收集 9
4. 全基因組基因型分型 9
5. 相關性分析品管 10
6. 基因型填補 10
7. 全基因組相關分析 10
8. 全基因組顯著性的閾值 11
第三章 結果 12
1. 基本生理檢測資料 12
2. 關聯性分析結果 12
3. 與FGF21高關聯性變異點 12
第四章 討論 14
圖一 4
圖二 5
圖三 7
圖四 19
圖五 20
圖六 21
表一 17
表二 18
第五章 參考文獻 26
dc.language.isozh-TW
dc.subject纖維母細胞生長因子21zh_TW
dc.subject內分泌zh_TW
dc.subject全基因組關聯性分析zh_TW
dc.subjectGenome-wide association studyen
dc.subjectFGF-21en
dc.subjectendocrineen
dc.title血清FGF21濃度之全基因組相關性分析zh_TW
dc.titleGenome-Wide Association Study of Serum FGF21 Levelsen
dc.typeThesis
dc.date.schoolyear107-2
dc.description.degree碩士
dc.contributor.oralexamcommittee陳沛隆(Pei-Lung Chen),施翔蓉(Shiang-Rong Shih),劉碧華(Pi-Wua Liu)
dc.subject.keyword纖維母細胞生長因子21,內分泌,全基因組關聯性分析,zh_TW
dc.subject.keywordFGF-21,endocrine,Genome-wide association study,en
dc.relation.page27
dc.identifier.doi10.6342/NTU201902695
dc.rights.note有償授權
dc.date.accepted2019-08-19
dc.contributor.author-college醫學院zh_TW
dc.contributor.author-dept分子醫學研究所zh_TW
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