茶叶科学
茶葉科學
다협과학
2013年
2期
109-115
,共7页
韦康%王丽鸳%成浩*%龚武云%吴立赟
韋康%王麗鴛%成浩*%龔武雲%吳立赟
위강%왕려원%성호*%공무운%오립빈
数字表达谱%茶苗%差异表达基因%光合作用
數字錶達譜%茶苗%差異錶達基因%光閤作用
수자표체보%다묘%차이표체기인%광합작용
digital gene expression profiling%tea cutting%differentially expressed genes%photosynthesis
利用数字基因表达谱技术研究了温湿度变化对秋插茶苗芽萌发基因表达的影响.通过保温棚处理日均温度提高约5.15℃,湿度提高5.10%,两者茶苗芽萌发具有明显差异.比较保温棚与对照芽的基因表达共筛选获得949个差异表达基因,其中503个基因受保温棚处理诱导上调表达,446个基因下调表达.对差异表达基因进行 GO 分类分析,在 P 值<0.01的情况下,有360个基因与14个 GO 分类匹配.其中7个 GO 分类与光合作用相关,P 值最小的 GO 分类为光系统,其11个基因均表现为上调表达,说明高温高湿条件具有促进光合相关基因表达的作用.这些结果将为深入研究理解茶苗的生长机制及相关基因的克隆打下基础.
利用數字基因錶達譜技術研究瞭溫濕度變化對鞦插茶苗芽萌髮基因錶達的影響.通過保溫棚處理日均溫度提高約5.15℃,濕度提高5.10%,兩者茶苗芽萌髮具有明顯差異.比較保溫棚與對照芽的基因錶達共篩選穫得949箇差異錶達基因,其中503箇基因受保溫棚處理誘導上調錶達,446箇基因下調錶達.對差異錶達基因進行 GO 分類分析,在 P 值<0.01的情況下,有360箇基因與14箇 GO 分類匹配.其中7箇 GO 分類與光閤作用相關,P 值最小的 GO 分類為光繫統,其11箇基因均錶現為上調錶達,說明高溫高濕條件具有促進光閤相關基因錶達的作用.這些結果將為深入研究理解茶苗的生長機製及相關基因的剋隆打下基礎.
이용수자기인표체보기술연구료온습도변화대추삽다묘아맹발기인표체적영향.통과보온붕처리일균온도제고약5.15℃,습도제고5.10%,량자다묘아맹발구유명현차이.비교보온붕여대조아적기인표체공사선획득949개차이표체기인,기중503개기인수보온붕처리유도상조표체,446개기인하조표체.대차이표체기인진행 GO 분류분석,재 P 치<0.01적정황하,유360개기인여14개 GO 분류필배.기중7개 GO 분류여광합작용상관,P 치최소적 GO 분류위광계통,기11개기인균표현위상조표체,설명고온고습조건구유촉진광합상관기인표체적작용.저사결과장위심입연구리해다묘적생장궤제급상관기인적극륭타하기출.
Differences of gene expression in buds of tea cuttings in response to temperature and humidity changes were studied. The daily temperature and humidity increased by 5.15℃ and 5.10% under plastic shading treatment. Meanwhile, bud expansion of tea cuttings under plastic shading was clearly different from that of control. After digital gene expression profiling analysis, a total of 949 differential expressed genes were obtained, including 503 up- and 446 down-regulated genes from buds of tea cuttings in plastic shed. Gene Ontology (GO) analysis showed that 360 genes were classified into 14 GO terms when P value <0.01. Seven GO terms were associated with photosynthesis. The GO term with the least P value was related to photosystem, which suggest high temperature and humidity are favorable for the induction of genes associated with photosynthesis. This study might provide new insight into understanding the mechanism of rapid propagation and related gene cloning in Camellia sinensis.