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  1. NTU Theses and Dissertations Repository
  2. 醫學院
  3. 微生物學科所
請用此 Handle URI 來引用此文件: http://tdr.lib.ntu.edu.tw/jspui/handle/123456789/78936
完整後設資料紀錄
DC 欄位值語言
dc.contributor.advisor詹世鵬zh_TW
dc.contributor.author王于箴zh_TW
dc.contributor.authorYu-Chen Wangen
dc.date.accessioned2021-07-11T15:30:31Z-
dc.date.available2024-02-28-
dc.date.copyright2018-10-09-
dc.date.issued2018-
dc.date.submitted2002-01-01-
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14. Cetkovic, H., et al., Nme family of proteins--clues from simple animals. Naunyn Schmiedebergs Arch Pharmacol, 2015. 388(2): p. 133-42.
15. Boissan, M., et al., The mammalian Nm23/NDPK family: from metastasis control to cilia movement. Mol Cell Biochem, 2009. 329(1-2): p. 51-62.
16. Tokarska-Schlattner, M., et al., The nucleoside diphosphate kinase D (NM23-H4) binds the inner mitochondrial membrane with high affinity to cardiolipin and couples nucleotide transfer with respiration. J Biol Chem, 2008. 283(38): p. 26198-207.
17. Mishra, P. and D.C. Chan, Metabolic regulation of mitochondrial dynamics. J Cell Biol, 2016. 212(4): p. 379-87.
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22. Scott, T.A., et al., Host-Microbe Co-metabolism Dictates Cancer Drug Efficacy in C. elegans. Cell, 2017. 169(3): p. 442-456 e18.
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dc.identifier.urihttp://tdr.lib.ntu.edu.tw/jspui/handle/123456789/78936-
dc.description.abstract粒線體融合和分裂現象的不平衡參與調控癌症生成,Non-Metastatic 4 (NME4)是位在粒線體的核苷酸二磷酸激酶,其主要參與在粒線體融合的過程中。有趣的是,我們先前的結果顯示在人類細胞中,腫瘤抑制子let-7 miRNA可能調控NME4,使我們想尋找let-7 miRNA與粒線體的關聯性以及其生理上的意義。由於以線蟲研究let-7的功能和表型有許多優點,本篇研究使用線蟲作為模式生物,測定線蟲中NME4同源基因ndk-1是否會受到let-7調控。而我們也確實發現在線蟲中降低ndk-1基因表現會像在人類細胞中降低NME4一樣造成粒線體碎片化,且在mid L4階段的let-7(n2853)線蟲中,碎片化粒線體的比例也顯著下降,我們的實驗結果指出let-7可能影響粒線體型態,而我們的研究也是第一個嘗試探討let-7和粒線體型態功能上的關聯性,這有助於發現新的miRNA對於調控粒線體動態平衡的路徑。zh_TW
dc.description.abstractImbalance of mitochondrial fission and fusion activities has been implicated in carcinogenesis. NME4, a mitochondria-localized nucleoside diphosphate kinase, is involved in mitochondrial fusion process. Interestingly, our previous results showed that the tumor suppressor miRNA let-7 seems to regulate NME4 in human cells, inspiring us to seek possible functional connection for let-7 miRNA to mitochondrial and the biological implication for this connection. In this study, we chose C. elegans as the model organism due to its advantages in studying let-7 function and phenotypes. We seek to determine whether the NME4 homolog ndk-1 in C. elegans is also regulated by let-7. Indeed, like NME4 in human cells, knockdown of ndk-1 in C. elegans caused mitochondrial fragmentation. In addition, we found that fragmentation of mitochondria is significantly reduced in let-7(n2853) mutants at the mid L4 stage. These results suggest that let-7 may play a role in mitochondrial morphology. Our study is the first attempt to examine function relevance of let-7 to mitochondria morphology and will help discover novel pathways for miRNAs to control mitochondrial dynamics.en
dc.description.provenanceMade available in DSpace on 2021-07-11T15:30:31Z (GMT). No. of bitstreams: 1
ntu-107-R05445124-1.pdf: 5918100 bytes, checksum: da1b8a783e1af5581c7b50fa150be490 (MD5)
Previous issue date: 2018
en
dc.description.tableofcontents誌謝 I
摘要 II
Abstract III
Chapter 1 Introduction 1
The let-7 miRNA 1
The role of the let-7 miRNA in C. elegans development 1
The let-7 miRNA is evolutionarily conserved 1
The let-7 miRNA is regarded as a tumor suppressor 2
NME4 may be a novel let-7 target gene 2
NME4 3
The NME family 3
The role of NME4 in mitochondrial fusion 3
Relevance of NME4 and mitochondrial dynamics in cancer 3
Association of NME4 and the let-7 miRNA 4
The C. elegans NME4 homolog ndk-1 4
Mitochondria-associated NDPKs across species 5
Project proposal 5
Chapter 2 Materials and methods 6
E. coli strains 6
C. elegans strains 6
C. elegans culture conditions 7
Synchronous growth 7
RNA interference (RNAi) 7
Slide preparation 8
Genomic DNA extraction 8
RNA extraction 9
Quantitative real-time RT-PCR 10
DNase treatment 10
cDNA synthesis 10
qRT-PCR 11
Construction of plasmids 12
Mitochondrial staining 15
Mitochondrial imaging 15
Mitochondrial morphologies analysis 15
Microinjection 16
Strain crosses 17
Single worm PCR 17
Detection of let-7(n2853) point mutation 18
Chapter 3 Results 19
C. elegans NDK-1 may function similarly to human NME4 that participates in mitochondrial fusion. 19
The let-7 miRNA plays a role in mitochondria dynamics at the mid L4 stage. 21
Mitochondrial dynamic seems to maintain balance in vulva in let-7(n2853) at the mid L4 stage. 22
Chapter 4 Discussion 24
Figures 26
Figure 1 26
Figure 2 29
Figure 3 33
Figure 4 37
References 39
Appendix 44
Appendix 1 44
Appendix 2 45
Appendix 3 47
Appendix 4 48
Appendix 5 51
Appendix 6 54
Appendix 7 56
Appendix 8 58
Appendix 9 59
Appendix 10 60
-
dc.language.isoen-
dc.subjectlet-7微小核醣核酸zh_TW
dc.subjectNDK-1zh_TW
dc.subjectNME4zh_TW
dc.subject核?酸二磷酸激?zh_TW
dc.subjectNDK-1en
dc.subjectlet-7 miRNAen
dc.subjectnucleoside diphosphate kinaseen
dc.subjectNME4en
dc.title測定在線蟲中NME4同源基因ndk-1是否受到let-7微小核糖核酸調控zh_TW
dc.titleDetermine whether the C. elegans NME4 homolog ndk-1 is regulated by the let-7 miRNAen
dc.typeThesis-
dc.date.schoolyear106-2-
dc.description.degree碩士-
dc.contributor.oralexamcommittee潘俊良;羅時成zh_TW
dc.contributor.oralexamcommittee;;en
dc.subject.keywordlet-7微小核醣核酸,核?酸二磷酸激?,NME4,NDK-1,zh_TW
dc.subject.keywordlet-7 miRNA,nucleoside diphosphate kinase,NME4,NDK-1,en
dc.relation.page60-
dc.identifier.doi10.6342/NTU201803824-
dc.rights.note未授權-
dc.date.accepted2018-08-17-
dc.contributor.author-college醫學院-
dc.contributor.author-dept微生物學研究所-
dc.date.embargo-lift2023-08-17-
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