Sinha Pallavi, Saxena Rachit K, Singh Vikas K, Krishnamurthy L, Varshney Rajeev K
Applied Genomics, Centre of Excellence in Genomics, International Crops Research Institute for the Semi-Arid Tropics Hyderabad, India.
Applied Genomics, Centre of Excellence in Genomics, International Crops Research Institute for the Semi-Arid TropicsHyderabad, India; School of Plant Biology and Institute of Agriculture, The University of Western Australia, PerthWA, Australia.
Front Plant Sci. 2015 Dec 21;6:1071. doi: 10.3389/fpls.2015.01071. eCollection 2015.
To identify stable housekeeping genes as a reference for expression analysis under heat and salt stress conditions in pigeonpea, the relative expression variation for 10 commonly used housekeeping genes (EF1α, UBQ10, GAPDH, 18Sr RNA, 25Sr RNA, TUB6, ACT1, IF4α, UBC, and HSP90) was studied in root, stem, and leaves tissues of Asha (ICPL 87119), a leading pigeonpea variety. Three statistical algorithms geNorm, NormFinder, and BestKeeper were used to define the stability of candidate genes. Under heat stress, UBC, HSP90, and GAPDH were found to be the most stable reference genes. In the case of salinity stress, GAPDH followed by UBC and HSP90 were identified to be the most stable reference genes. Subsequently, the above identified genes were validated using qRT-PCR based gene expression analysis of two universal stress-resposive genes namely uspA and uspB. The relative quantification of these two genes varied according to the internal controls (most stable, least stable, and combination of most stable and least stable housekeeping genes) and thus confirmed the choice as well as validation of internal controls in such experiments. The identified and validated housekeeping genes will facilitate gene expression studies under heat and salt stress conditions in pigeonpea.
为了鉴定稳定的看家基因,作为木豆在热胁迫和盐胁迫条件下表达分析的参照,研究了10个常用看家基因(EF1α、UBQ10、GAPDH、18Sr RNA、25Sr RNA、TUB6、ACT1、IF4α、UBC和HSP90)在木豆主栽品种阿莎(ICPL 87119)的根、茎和叶组织中的相对表达变化。使用geNorm、NormFinder和BestKeeper三种统计算法来确定候选基因的稳定性。在热胁迫下,发现UBC、HSP90和GAPDH是最稳定的参照基因。在盐胁迫情况下,确定GAPDH其次是UBC和HSP90是最稳定的参照基因。随后,通过对两个普遍的胁迫响应基因uspA和uspB进行基于qRT-PCR的基因表达分析,对上述鉴定出的基因进行了验证。这两个基因的相对定量根据内参(最稳定、最不稳定以及最稳定和最不稳定看家基因的组合)而变化,从而证实了在此类实验中内参的选择及验证。鉴定和验证的看家基因将有助于木豆在热胁迫和盐胁迫条件下的基因表达研究。