题名 |
阿拉伯芥atToc159轉運蛋白基因的細胞專一性表現與領先內插子對基因表現的影響 |
并列篇名 |
Cell-type Specific and Leader Intron-regulated Expression of Arabidopsis atToc159 Translocon Gene Family |
DOI |
10.6248/BF.2013.48.05 |
作者 |
劉玉山(Yu-Shan Liu);孫智雯(Chih-Wen Sun) |
关键词 |
阿拉伯芥 ; atToc159基因表現 ; 領先內插子 ; GUS報導基因 ; 保衛細胞 ; Arabidopsis ; atToc159 gene expression ; leader intron ; GUS reporter gene ; guard cells |
期刊名称 |
Bio Formosa |
卷期/出版年月 |
48卷(2013 / 06 / 01) |
页次 |
33 - 44 |
内容语文 |
繁體中文 |
中文摘要 |
根據蛋白質胺基酸序列的相似度與運輸蛋白質種類的不同,可將阿拉伯芥四種Toc159的同源蛋白質,分成atToc159/atToc90和atToc132/atToc120兩大群。其中atToc159/atToc90被認為與辨識和運輸光合作用蛋白質有關,atToc132/atToc120則可能負責辨識和運輸非光合作用蛋白。在阿拉伯芥生長發育的過程中,這些轉運蛋白的基因必須被適當的調控,否則色質體的發育與生理將因缺乏必需的蛋白質的輸入而被抑制。為了解atToc159基因家族的表現機制,轉殖分別攜帶不同長度的基因上游調控序列的重組質體進入野生型阿拉伯芥,以獲得穩定轉殖的植株。分析這些轉殖植株中營養器官的GUS酵素活性及mRNA表現量,發現atToc159、atToc132/90和atToc120基因在七天齡的幼苗中分別有最高,次之及最低的表現量。此外,位於atToc120和atToc90的5’ UTR內的領先內插子序列會明顯增加其基因表現量。進一步探討光對內插子在基因表現上的影響,比較生長在光照和黑暗條件下的120PUI和120P轉殖株的GUS 表現量,我們發現黑暗會提高內插子效應。除了進行不同組織的基因表現之比較分析外,我們也進行了這些轉殖株中基因的細胞專一性表現的研究。令人驚訝的,在與atToc159和atToc132的比較下,atToc90和atToc120在子葉保衛細胞中基因的表現量明顯地要比葉肉細胞多,這顯示atToc90和atToc120在保衛細胞運輸蛋白質進入葉綠體上可能扮演一定的角色。這些研究結果支持葉綠體轉運蛋白atToc159基因家族之基因的表現量在不同的組織和發育階段的差異,可能是受到不同的發育和環境的因子刺激所調節。 |
英文摘要 |
In Arabidopsis, four Toc159 homologues are reported and could be classified to two subgroups, atToc159/atToc90 and atToc132/atToc120, based on their sequence homology and substrate specificity. Therefore, expression of these translocon genes have to be regulated properly, otherwise the development and maintenance of plastids would be prohibited due to lack of essential protein import. In order to reveal the regulatory mechanism of atToc159 gene family members, transgenes containing various lengths of the upstream sequences of these translocon genes and GUS coding sequence were transferred to wild-type Arabidopsis. The steady accumulation of GUS expression from the vegetative tissues of these transformants was examined first. In general, atToc159, atToc132/atToc90, and atToc120 have relatively high, moderate, and low expression levels in various tissues of 7-day-old seeldings. Furthermore, the expression of atToc120 and atToc90 could be up-regulated by their corresponding leader intron sequence within 5' untranslated region (5' UTR) region. To further understand the intron effect of atToc120 expression was regulated by light, the GUS activity of 120PUI and 120P plants grown under light/dark cycle and continuous dark conditions were compared. Our data suggests that the intron sequence of atToc120 is more responsive to dark signal. In addition to tissue-specific expression, the cell-specific expression of these transgenic plants was also determined. Surprisedly, atToc90 and atToc120 had higher GUS activity in the guard cells than mesophyll cells of cotyledon when compared to atToc159 and atToc132. This indicates that atToc90 and atToc120 might play a more important role in regulating chloroplast protein import of guard cells. These data support that the spatial and temporal expression of atToc159 gene family members is regulated by different developmental and environmental stimuli. |
主题分类 |
生物農學 >
生物科學 |