IDENTIFICATION OF OIL PALM ROOT-SPECIFIC GENES THROUGH MINING OF RNA-SEQ DATA AND RT-qPCR ANALYSIS

被引:3
作者
Masura, Subhi Siti [1 ,2 ]
Abd Rasid, Omar [1 ]
Shaharuddin, Noor Azmi [2 ,3 ]
Masani, Mat Yunus Abdul [1 ]
Chan, Kuang-Lim [1 ]
Low, Eng-Ti Leslie [1 ]
Bada, Siti Suriawati [1 ]
Hanin, Ayub Nor [1 ]
Rahmah, Abdul Rahman Siti [1 ]
Abdullah, Mohd Puad [2 ]
Azzeme, Azzreena Mohamad [2 ]
Parveez, Ghulam Kadir Ahmad [1 ]
机构
[1] Malaysian Palm Oil Board, 6 Persiaran Inst, Kajang 43000, Selangor, Malaysia
[2] Univ Putra Malaysia, Fac Biotechnol & Biomol Sci, Dept Biochem, Upm Serdang 43400, Selangor, Malaysia
[3] Univ Putra Malaysia, Inst Plantat Studies, Upm Serdang 43400, Selangor, Malaysia
来源
JOURNAL OF OIL PALM RESEARCH | 2022年 / 34卷 / 02期
关键词
Elaeis guineensis; root-specific genes; RNA-Seq; RT-qPCR; REFERENCE SEQUENCE REFSEQ; CELL-WALL PROTEIN; PROLINE-RICH; TRANSGENE EXPRESSION; QUANTITATIVE PCR; PROMOTER; ARABIDOPSIS; TISSUES; METALLOTHIONEINS; BIOTECHNOLOGY;
D O I
10.21894/jopr.2021.0036
中图分类号
TS2 [食品工业];
学科分类号
0832 ;
摘要
Identification of novel genes that are specifically expressed in root is essential for isolation and characterisation of root-specific promoters. Mining the transcriptome of various oil palm tissue-specific data generated from ribonucleic acid-sequencing (RNA-Seq) technology has enabled the discovery of rootspecific genes. A total of seven candidates of root-specifically or preferentially expressed genes were selected from RNA-Seq analysis, and the gene expression profiles were validated using real-time quantitative polymerase chain reaction (RT-qPCR). The relative fold change of transcript expression in RT-qPCR was statistically analysed by comparing with root tissues at the in vitro culture stage (RS1). Results showed that the transcript annotated as an oil palm metallothionine (EgMT) gene was significantly upregulated at around 7 to 170-fold across the different developmental stages of root tissues. A proline-rich protein (EgPRP1) transcript was also significantly upregulated by about 7 to 55-fold. Both EgMT and EgPRP1 transcripts had relatively low expressions in the other tissues studied. The high levels of expression of EgMT and EgPRP1 in roots highlighted the genes' promoter's potential to regulate a strong expression level of transgenes in a root-specific manner.
引用
收藏
页码:261 / 275
页数:15
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