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  1. 学位論文
  2. 博士論文
  3. 学位授与年月日:2017.03.24

Functional analysis of subcellular localization of oncogene products in Drosophila

http://hdl.handle.net/10212/2380
http://hdl.handle.net/10212/2380
5c32b93e-f2d3-4d43-8975-fe172c3b1441
名前 / ファイル ライセンス アクション
D1-0822_h1.pdf 全文 (9.1 MB)
D1-0822.pdf 内容・審査結果の要旨 (164.7 KB)
Item type 学位論文 / Thesis or Dissertation(1)
公開日 2019-01-15
タイトル
タイトル Functional analysis of subcellular localization of oncogene products in Drosophila
言語 en
その他のタイトル
その他のタイトル ショウジョウバエにおけるがん遺伝子産物の細胞内局在の機能解析
言語 ja
作成者 梅河内, 隆成

× 梅河内, 隆成

en Umegawachi, Takanari

ja 梅河内, 隆成

Search repository
アクセス権
アクセス権 open access
アクセス権URI http://purl.org/coar/access_right/c_abf2
主題
言語 en
主題Scheme Other
主題 mRNA localization
主題
言語 en
主題Scheme Other
主題 Endoplasmic reticulum
主題
言語 en
主題Scheme Other
主題 SRP-independent pathway
主題
言語 en
主題Scheme Other
主題 yorkie
主題
言語 en
主題Scheme Other
主題 Hippo pathway
内容記述
内容記述タイプ Abstract
内容記述 I investigate subcellular localization of two oncogene products. 1. Investigation of endoplasmic reticulum (ER) –targeting mechanism of oncogene yorkie mRNA yorkie (yki), the Drosophila homolog of human Yes-associated protein 1 (YAP1), is a oncogene conserved from Drosophila to humans. In multiple human cancers, elevated YAP1 expression has been observed and shown to promote tumor formation. Here I show that the amount of Yki protein is regulated by two novel regulatory mechanisms. I found that yki mRNA are associated with the ER and forms foci that partially colocalize to processing bodies in the vicinity of the ER. This localization is dependent on a stem-loop (SL2) structure in the 3’ untranslated region of yki mRNA. Surprisingly, the deletion of SL2 increases the amount of Yki protein and results in severe overgrowth phenotypes in eye imaginal discs. When the localization to the P-bodies is disrupted, Yki protein level increases without a significant effect on mRNA level. When the SL is completely removed, protein levels drastically increase, but in this case, due to increased RNA stability. In the latter case, we show that the increased RNA accumulation is due to removal of a putative miR-8 seed sequence in the SL2. These data demonstrate two novel regulatory mechanisms, both controlled by the yki SL2 element, that are essential for proper tissue growth regulation. 2. Functional analysis of nucleolus-localization of Rpd3 protein in starvation Epigenetic regulation in starvation is important but not fully understood yet. Recent studies have shown that epigenetic regulation is required for acquiring starvation stress resistance in cancer cell proliferation. Here I identified the Rpd3 gene, a Drosophila homolog of histone deacetylase 1, as a critical epigenetic regulator for acquiring starvation stress resistance. In response to starvation stress, the level of Rpd3 rapidly increased, and it accumulated in the nucleolus. I revealed that Rpd3 binds to the genomic region containing the rRNA promoters and activates rRNA synthesis in response to starvation stress. Polysome analyses revealed that the amount of polysomes was decreased in Rpd3 knockdown flies under starvation stress. Since the autophagy-related proteins are known to be starvation stress tolerance proteins, I examined autophagy activity and found that it was reduced in Rpd3 knockdown flies. Taken together, I conclude that Rpd3 accumulates in the nucleolus in the early stage of starvation, upregulates rRNA synthesis, maintains the polysome amount for translation, and finally increases stress tolerance proteins, such as autophagy-related proteins, to acquire starvation stress resistance.
言語 en
日付
日付 2017-03-24
日付タイプ Issued
言語
言語 eng
資源タイプ
資源タイプ識別子 http://purl.org/coar/resource_type/c_db06
資源タイプ doctoral thesis
出版タイプ
出版タイプ VoR
出版タイプResource http://purl.org/coar/version/c_970fb48d4fbd8a85
学位授与番号
学位授与番号 甲第822号
学位名
言語 ja
学位名 博士(学術)
学位授与年月日
学位授与年月日 2017-03-24
学位授与機関
学位授与機関識別子Scheme kakenhi
学位授与機関識別子 14303
言語 ja
学位授与機関名 京都工芸繊維大学
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