跳到主要內容

臺灣博碩士論文加值系統

(216.73.216.61) 您好!臺灣時間:2026/09/15 07:36
字體大小: 字級放大   字級縮小   預設字形  
回查詢結果 :::

詳目顯示

: 
twitterline
研究生:尤約書亞
研究生(外文):YU, YUEH SHU-YA
論文名稱:竹莖扁蚜不同型態個體之次世代定序轉錄體資料比較分析
論文名稱(外文):Next Generation Sequencing Based Transcriptome Analysis For Comparison of Different Morphs of Pseudoregma Bambucicola Takahashi (Hemiptera: Aphididae)
指導教授:王琄嬋
指導教授(外文):WANG, CHUAN-CHAN
口試委員:侯藹玲李後晶
口試委員(外文):HOUR, AI-LINGLEE, HOW-JING
口試日期:2018-07-16
學位類別:碩士
校院名稱:輔仁大學
系所名稱:生命科學系碩士班
學門:生命科學學門
學類:生物學類
論文種類:學術論文
論文出版年:2018
畢業學年度:106
語文別:中文
論文頁數:55
中文關鍵詞:竹莖扁蚜兵蚜表皮蛋白基因本體論
外文關鍵詞:Pseudoregma bambucicolaSoldierCuticle proteinGene ontology
相關次數:
  • 被引用被引用:0
  • 點閱點閱:403
  • 評分評分:
  • 下載下載:29
  • 收藏至我的研究室書目清單書目收藏:0
竹莖扁蚜(Pseudoregma bambucicola Takahashi)是一種具寄主轉換及造癭特性之社會性蚜蟲,在其生活史循環的大部分世代都是以孤雌生殖的方式繁殖,並展現出複雜的多表現型現象(polyphenism)。在寄主轉換過程中,會在一次寄主植物紅皮(Styrax suberifolius)上造癭並生活於蟲癭內部,在二次寄主植物竹子(Bambusa spp.)上則取食於竹子的莖部表面。不論在一次或二次寄主植物上,複雜的多表現型都包括有無翅型個體、有翅型個體及兵蚜,並且這三種型態的個體在兩種不同寄主植物上的外部形態也有明顯的差異。其中,最特殊的為不孕、形態特化且具防禦行為的兵蚜。為了瞭解兵蚜在分子層次上的特殊表現,本研究利用竹莖扁蚜在兩種寄主植物上的無翅型成蟲和兵蚜共四組轉錄體次世代定序(Next Generation Sequencing, NGS)資料,使用Weighted deviasion來篩選出有表現差異的基因,並以GO(Gene Ontology) enrichment來分析顯著表現的GO註解,最後用Web Gene Ontology Annotation Plot (WEGO)對顯著GO註解分類。結果,我們在不同比較組中找到300至800多不等的差異表現基因。刪去沒有GO註解的基因後,剩下100至300多不等的差異表現基因。經過GO顯著性分析和分類後,在結構分子(structural molecule)分類中找到和表皮結構成分有關的基因。經過整理後,我們發現竹莖扁蚜的兵蚜、無翅型成蟲在表皮結構相關的分類中有各自表現較高的基因,且一次寄主上的蚜蟲和二次寄主上的蚜蟲的表皮表現基因也有差異。差異表現的表皮基因中,有一個預測被歸類為R&R Consensus裡面的基因序列。最後,我們知道竹莖扁蚜的兵蚜有特別表現的基因,推測和表皮的結構有關。竹子兵蚜特別表現的基因則和肌肉的結構有關。
Pseudoregma bambucicola Takahashi is a social aphid characterized with host alternation and gall formation. It reproduces pathenogenetically in most of the generations within a life cycle. It also performs very complex polyphenism. During the process of host alternation, P. bambucicola utilizes Styrax suberifolius as its primary host plant and forms the gall to live and feed inside. Bamboos are used as its secondary host plant and P. bambucicola prefers to feed on the surface of the bamboo stem. On both the primary and the secondary host plants, P. bambucicola produces wingless females, winged females and soldiers. Among all these three types of aphids, soldiers are the most specialized morphs because it is sterile and with specialized defensive morphology and behavior. To uncover the molecular level characteristics of soldiers and non-soldiers, we compared the Next Generation Sequencing based transcriptome data between soldiers and wingless adults from both kinds of host plants. Weighted deviation was used to filter those differentially expressed genes. GO (Gene Ontology) enrichment was used to analyze the significantly expressed GO annotation. Finally, WEGO (Web Gene Ontology Annotation Plot) was used to compare and plot GO annotation results. We found 300~800 differentially expressed genes from different combinations of comparisons. After deleting genes without GO annotations, there were 100~300 differentially expressed genes left. After GO significance analysis and classification, we found that some genes classified within the category of Structural Molecular Activity are related to cuticle composition. We found that soldiers and wingless adults of P. bambucicola both have specific differentially expressed genes within the category of structural constituent of cuticle. Aphids from different host plants also reveal specific differentially expressed genes within the category of structural constituent of cuticle. In conclusion, we found that soldiers, regardless of host plants, of P. bambucicola have a specific differentially expressed gene which is related to cuticle constitution, and soldiers on bamboos have a specific differentially expressed gene which is related to muscle constitution.
摘要 i
Abstract ii
圖目錄 iv
表目錄 v
附錄目錄 vi
前言 1
研究目的 6
材料與方法 7
資料來源 7
Gene Ontology Annotation 8
基因表現差異分析 8
顯著GO term分析 9
Web Gene Ontology Annotation Plot 10
Basic Local Alignment Search Tool 10
結果 12
基因表現差異分析 12
GO顯著性分析 12
顯著GO分布 13
形態結構相關基因的整理和產物預測 15
討論 19
參考文獻 26
圖表 32
附錄 43

Andersen, S. O. 1998. Amino acid sequence studies on endocuticular proteins from the desert locust, Schistocerca gregaria. Insect Biochemistry and Molecular Biology 28: 421-434.
Andersen, S. O. 2000. Studies on proteins in post-ecdysial nymphal cuticle of locust, Locusta migratoria, and cockroach, Blaberus craniifer. Insect Biochemistry and Molecular Biology 30: 569-577.
Aoki, S. 1977. Colophina clematis (Homoptera, Pemphigidae), an aphid Species
with" Soldiers". Kontyû 45: 276-282.
Aoki, S. 1987. Evolution of sterile soldiers in aphids. In “Animal Societies: Theories and Facts”, Japan Scientific Societies Press, Tokyo, page 53-65.
Aoki, S., S. Akimoto and S. Yamane. 1981. Observations on Pseudoregma alexanderi (Homoptera, Pemphigidae), an aphid species producing pseudoscorpion-like soldiers on bamboos. Kontyû 49: 355-366.
Aoki, S. and U. Kurosu. 1992. Gall generations of the soldier-producing aphid
Pseudoregma bambucicola (Homoptera). Kontyû 60: 359-368.
Aoki, S. and U. Kurosu. 2010. A review of the biology of Cerataphidini (Hemiptera, Aphididae, Hormaphidinae), focusing mainly on their life cycles, gall formation, and soldiers. Psyche 2010: 1-34, Article ID 380351.
Ashburner, M., C. A. Ball, J. A. Blake, D. Botstein, H. Butler, J. M. Cherry, A. P. Davis, K. Dolinski, S. S. Dwight, J. T. Eppig, M. A. Harris, D. P. Hill, L. Issel-Tarver, A. Kasarskis, S. Lewis, J. C. Matese, J. E. Richardson, M. Ringwald, G. M. Rubin and G. Sherlock. 2000. Gene ontology: tool for the unification of biology. Nature Genetics 25: 25-29.
Audic, S. and J.-M. Claverie. 1997. The significance of digital gene expression profiles. Genome Research 7: 986-995.
Cao, J. and S. Zhang. 2014. A Bayesian extension of the hypergeometric test for
functional enrichment analysis. Biometrics 70: 84-94.
Chang, C. 2011. Statistical analysis of rice SAGE and MPSS data. Master’s Thesis of Department of Life Science, Fu Jen Catholic University, Taiwan.
Chen, T.-W., R.-C. R. Gan, T. H. Wu, P.-J. Huang, C.-Y. Lee, Y.-Y. M. Chen, C.-C. Chen and P. Tang. 2012. FastAnnotator-an efficient transcript annotation web tool. BMC Genomics 13( Suppl 7): S9.

Chen, X., W. Xiong, C. Li, S. Gao, X. Song, W. Wu and B. Li. 2016. Comparative
RNA-sequencing profiling reveals novel Delta-class glutathione S-transferases relative genes expression patterns in Tribolium castaneum. Gene 593: 13-20.
Cortes, T., D. Tagu, J. Simon, A. Moya and D. Martinez-Torres. 2008. Sex versus
parthenogenesis: a transcriptomic approach of photoperiod response in the model aphid Acyrthosiphon pisum (Hemiptera: Aphididae). Gene 408: 146-156.
Dombrovsky, A., I. Sobolev, N. Chejanovsky and B. Raccah. 2007. Characterization of RR-1 and RR-2 cuticular proteins from Myzus persicae. Comparative Biochemistry and Physiology Part B: Biochemistry and Molecular Biology 146: 256-264.
Dwight, S. S., M. A. Harris, K. Dolinski, C. A. Ball, G. Binkley, K. R. Christie, D. G. Fisk, L. Issel-Tarver, M. Schroeder and G. Sherlock. 2002. Saccharomyces Genome Database (SGD) provides secondary gene annotation using the Gene Ontology (GO). Nucleic Acids Research 30: 69-72.
Fu, C., M. Xu, X. Chen, X. Sheng, Z. Yuan, Y. Liu, H. Li, Z. Sun, H. Li and L. Yang. 2017. next-generation sequencing. Journal of Medical Genetics 54: 190-195.
Fukatsu, T., A. Sarjiya and H. Shibao. 2005. Soldier caste with morphological and reproductive division in the aphid tribe Nipponaphidini. Insectes Sociaux 52: 132-138.
Gallot, A., C. Rispe, N. Leterme, J.-P. Gauthier, S. Jaubert-Possamai and D. Tagu. 2010. Cuticular proteins and seasonal photoperiodism in aphids. Insect Biochemistry and Molecular Biology 40: 235-240.
Harris, M. A., J. Clark, A. Ireland, J. Lomax, M. Ashburner, R. Foulger, K. Eilbeck, S. Lewis, B. Marshall, C. Mungall, J. Richter, G. M. Rubin, J. A. Blake, C. Bult, M. Dolan, H. Drabkin, J. T. Eppig, D. P. Hill, L. Ni, M. Ringwald, R. Balakrishnan, J. M. Cherry, K. R. Christie, M. C. Costanzo, S. S. Dwight, S. Engel, D. G. Fisk, J. E. Hirschman, E. L. Hong, R. S. Nash, A. Sethuraman, C. L. Theesfeld, D. Botstein, K. Dolinski, B. Feierbach, T. Berardini, S. Mundodi, S. Y. Rhee, R. Apweiler, D. Barrell, E. Camon, E. Dimmer, V. Lee, R. Chisholm, P. Gaudet, W. Kibbe, R. Kishore, E. M. Schwarz, P. Sternberg, M. Gwinn, L. Hannick, J. Wortman, M. Berriman, V. Wood, N. de la Cruz, P. Tonellato, P. Jaiswal, T. Seigfried and R. White. 2004. The Gene Ontology (GO) database and informatics resource. Nucleic Acids Research 32(Database issue): D258-261.
Hattori, M., O. Kishida and T. Itino. 2013. Soldiers with large weapons in
predator-abundant midsummer: phenotypic plasticity in a eusocial aphid. Evolutionary Ecology 27: 847-862.

Hattori, M., O. Kishida and T. Itino. 2017. Soldiers with large weapons behave
aggressively against predators: correlated morphological and behavioral defensive traits in a eusocial aphid. Insectes Sociaux 64: 39-44.
Holman, L., C. G. Jørgensen, J. Nielsen and P. d'Ettorre. 2010. Identification of an ant queen pheromone regulating worker sterility. Proceedings of the Royal Society of London B 277: 3793-3800.
Itô, Y. 1989. The evolutionary biology of sterile soldiers in aphids. Trends in Ecology and Evolotion 4: 69-73.
Itô, Y., S. Tanaka, J. Yukawa and K. Tsuji. 1995. Factors affecting the proportion of soldiers in eusocial bamboo aphid, Pseudoregma bambucicola, colonies. Ethology Ecology and Evolution 7: 335-345.
Jackson, L. L. and G. L. Baker. 1970. Cuticular lipids of insects. Lipids 5: 239-246.
Jedličková, V., P. Jedlička and H.-J. Lee. 2015. Characterization and expression analysis of adipokinetic hormone and its receptor in eusocial aphid Pseudoregma bambucicola. General and Comparative Endocrinology 223: 38-46.
Kutsukake, M., H. Shibao, N. Nikoh, M. Morioka, T. Tamura, T. Hoshino, S. Ohgiya and T. Fukatsu. 2004. Venomous protease of aphid soldier for colony defense. Proceedings of the National Academy of Sciences of the United States of America 101: 11338-11343.
Le Trionnaire, G., J. Hardie, S. Jaubert‐Possamai, J. C. Simon and D. Tagu. 2008. Shifting from clonal to sexual reproduction in aphids: physiological and developmental aspects. Biology of the Cell 100: 441-451.
Le Trionnaire, G., S. Jaubert, B. Sabater-Munoz, A. Benedetto, J. Bonhomme, N.
Prunier-Leterme, D. Martinez-Torres, J.-C. Simon and D. Tagu. 2007. Seasonal photoperiodism regulates the expression of cuticular and signalling protein genes in the pea aphid. Insect Biochemistry and Molecular Biology 37: 1094-1102.
Lees, A. 1964. The location of the photoperiodic receptors in the aphid Megoura
viciae Buckton. Journal of Experimental Biology 41: 119-133.
Mardis, E. R. 2008. The impact of next-generation sequencing technology on
genetics. Trends in Genetics 24: 133-141.
Metzker, M. L. 2010. Sequencing technologies—the next generation. Nature Reviews Genetics 11: 31-46.
Moran, N. A. 1988. The evolution of host-plant alternation in aphids: evidence for specialization as a dead end. The American Naturalist 132: 681-706.
Nieto Nafria, J., M. Mier Durante and G. Remaudière. 1997. Les noms des taxa du
groupe-famille chez les Aphididae [Hemiptera]. Revue Française d'entomologie 19: 77-92.
Noh, M. Y., S. Muthukrishnan, K. J. Kramer and Y. Arakane. 2015. Tribolium
castaneum RR-1 cuticular protein TcCPR4 is required for formation of pore canals in rigid cuticle. PLoS Genetics 11: e1004963.
Ohara, K. 1985. Observations on the prey-predator relationship between
Pseudoregma bambucicola (Homoptera, Pemphigidae) and Metasyrphus confrater (Diptera, Syrphidae), with special reference to the behaviour of the aphid soldiers. Esakia 23: 107-110.
Oi, C. A., J. S. van Zweden, R. C. Oliveira, A. Van Oystaeyen, F. S. Nascimento and T. Wenseleers. 2015. The origin and evolution of social insect queen pheromones: Novel hypotheses and outstanding problems. Bioessays 37: 808-821.
Rebers, J. E. and L. M. Riddiford. 1988. Structure and expression of a Manduca sexta larval cuticle gene homologous to Drosophila cuticle genes. Journal of Molecular Biology 203: 411-423.
Reuner, A., S. Hengherr, B. Mali, F. Förster, D. Arndt, R. Reinhardt, T. Dandekar, M. Frohme, F. Brümmer and R. O. Schill. 2010. Stress response in tardigrades: differential gene expression of molecular chaperones. Cell Stress and Chaperones 15: 423-430.
Sakata, K., Y. Itô, J. Yukawa and S. Yamane. 1991. Ratio of sterile soldiers in the bamboo aphid, Pseudoregma bambucicola (Homoptera: Aphididae), colonies in relation to social and habitat conditions. Applied Entomology and Zoology 26: 463-468.
Shang, F., B.-Y. Ding, Y. Xiong, W. Dou, D. Wei, H.-B. Jiang, D.-D. Wei and J.-J. Wang. 2016. Differential expression of genes in the alate and apterous morphs of the brown citrus aphid, Toxoptera citricida. Scientific Reports 6: 32099.
Shibao, H. 1998. Social structure and the defensive role of soldiers in a eusocial bamboo aphid, Pseudoregma bambucicola (Homoptera: Aphididae): a test of the defence-optimization hypothesis. Researches on Population Ecology 40: 325-333.
Shibao, H. 1999. Reproductive schedule and factors affecting soldier production in the eusocial bamboo aphid Pseudoregma bambucicola (Homoptera, Aphididae). Insectes Sociaux 46: 378-386.
Shibao, H., M. Kutsukake, S. Matsuyama, T. Fukatsu and M. Shimada. 2010. Mechanisms regulating caste differentiation in an aphid social system. Communicative and Integrative Biology 3: 1-5.
Shibao, H., M. Morimoto, Y. Okumura and M. Shimada. 2009. Fitness costs and
benefits of ant attendance and soldier production for the social aphid Pseudoregma bambucicola (Homoptera: Aphididae: Hormaphidinae). Sociobiology 54: 673-698.
Soares, M. P., M. Elias-Neto, Z. L. Simões and M. M. Bitondi. 2007. A cuticle protein gene in the honeybee: expression during development and in relation to the ecdysteroid titer. Insect Biochemistry and Molecular Biology 37: 1272-1282.
Sobotka, J. A., M. Daley, S. Chandrasekaran, B. D. Rubin and G. J. Thompson. 2016. Structure and function of gene regulatory networks associated with worker sterility in honeybees. Ecology and Evolution 6: 1692-1701.
Steel, C. and A. Lees. 1977. The role of neurosecretion in the photoperiodic control of polymorphism in the aphid Megoura viciae. Journal of Experimental Biology 67: 117-135.
Stern, D. L. 1998. Phylogeny of the tribe Cerataphidini (Homoptera) and the
evolution of the horned soldier aphids. Evolution 52: 155-165.
Stern, D. L. and W. A. Foster. 1996. The evolution of soldiers in aphids. Biological Reviews 71: 27-79.
Stern, D. L. and W. A. Foster. 1997. The evolution of sociality in aphids: a clone’s-eye view. In “The Evolution of Social Behavior in Insects and Arachnids”, Cambridge University Press, Cambridge, page 150-165.
Sunose, T., S. Yamane, K. Tsuda and K. Takasu. 1991. What do the soldiers of
Pseudoregma bambucicola (Homoptera, Aphidoidea) defend? Kontyû 59: 141-148.
Tavazoie, S., J. D. Hughes, M. J. Campbell, R. J. Cho and G. M. Church. 1999.
Systematic determination of genetic network architecture. Nature Genetics 22: 281-285.
Tian, L. and X. Zhou. 2014. The soldiers in societies: defense, regulation, and
evolution. International Journal of Biological Sciences 10: 296.
Togawa, T., H. Nakato and S. Izumi. 2004. Analysis of the chitin recognition
mechanism of cuticle proteins from the soft cuticle of the silkworm, Bombyx mori. Insect Biochemistry and Molecular Biology 34: 1059-1067.
Vannini, L. and J. H. Willis. 2017. Localization of RR-1 and RR-2 cuticular proteins within the cuticle of Anopheles gambiae. Arthropod Structure and Development 46: 13-29.
Wang, C.-C., S.-C. Tsaur, U. Kurosu, S. Aoki and H.-J. Lee. 2008. Social parasitism and behavioral interactions between two gall-forming social aphids. Insectes Sociaux 55: 147-152.
Willis, J. H., V. A. Iconomidou, R. F. Smith and S. J. Hamodrakas. 2005. Cuticular proteins, In “ Comprehensive Molecular Insect Science”, Elsevier, Amsterdam, page 79-109.
Wojciechowski, W. 1992. Studies on the systematic system of aphids (Homoptera,
Aphidinea), Uniwersytet Slaski, Katowice, Poland.
Ye, J., L. Fang, H. Zheng, Y. Zhang, J. Chen, Z. Zhang, J. Wang, S. Li, R. Li, L. Bolund and J. Wang. 2006. WEGO: a web tool for plotting GO annotations. Nucleic Acids Research 34(Web Server issue): W293-297.
Yoshiyasu, Y. and K. Ohara. 1982. A new aphidophagous species of a phycitine genus Cryptoblabes from Japan (Lepidoptera, Pyralidae). Lepidoptera Science 33: 51-60.

QRCODE
 
 
 
 
 
                                                                                                                                                                                                                                                                                                                                                                                                               
第一頁 上一頁 下一頁 最後一頁 top