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Genomic Survey Characterization and Expression Profile Analysis of the SBP Genes in Pineapple (Ananas comosus L.)

机译:菠萝(Ananas comosus L.)SBP基因的基因组调查表征和表达谱分析

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摘要

Gene expression is regulated by transcription factors, which play many significant developmental processes. SQUAMOSA promoter-binding proteins (SBP) perform a variety of regulatory functions in leaf, flower, and fruit development, plant architecture, and sporogenesis. 16 SBP genes were identified in pineapple and were divided into four groups on basis of phylogenetic analysis. Five paralogs in pineapple for SBP genes were identified with Ka/Ks ratio varied from 0.20 for AcSBP14 and AcSBP15 to 0.36 for AcSBP6 and AcSBP16, respectively. 16 SBP genes were located on 12 chromosomes out of 25 pineapple chromosomes with highly conserved protein sequence structures. The isoionic points of SBP ranged from 6.05 to 9.57, while molecular weight varied from 22.7 to 121.9 kD. Expression profiles of SBP genes revealed that AcSBP7 and AcSBP15 (leaf), AcSBP13, AcSBP12, AcSBP8, AcSBP16, AcSBP9, and AcSBP11 (sepal), AcSBP6, AcSBP4, and AcSBP10 (stamen), AcSBP14, AcSBP1, and AcSBP5 (fruit) while the rest of genes showed low expression in studied tissues. Four genes, that is, AcSBP11, AcSBP6, AcSBP4, and AcSBP12, were highly expressed at 4°C, while AcSBP16 were upregulated at 45°C. RNA-Seq was validated through qRT-PCR for some genes. Salt stress-induced expression of two genes, that is, AcSBP7 and AcSBP14, while in drought stress, AcSBP12 and AcSBP15 were highly expressed. Our study lays a foundation for further gene function and expression studies of SBP genes in pineapple.
机译:基因表达受转录因子的调控,转录因子具有许多重要的发育过程。 SQUAMOSA启动子结合蛋白(SBP)在叶,花和果实的发育,植物结构和孢子发生中执行多种调控功能。在菠萝中鉴定出16个SBP基因,并根据系统发育分析将其分为4组。在菠萝中发现了五个SBP基因旁系同源物,Ka / Ks比分别从AcSBP14和AcSBP15的0.20到AcSBP6和AcSBP16的0.36。 16个SBP基因位于25个菠萝染色体中的12个染色体上,具有高度保守的蛋白质序列结构。 SBP的等离子点范围为6.05至9.57,而分子量范围为22.7至121.9 kD。 SBP基因的表达谱显示,AcSBP7和AcSBP15(叶),AcSBP13,AcSBP12,AcSBP8,AcSBP16,AcSBP9和AcSBP11(sepal), AcSBP6 AcSBP4 和< em> AcSBP10 (雄蕊), AcSBP14 AcSBP1 AcSBP5 (果实),而其余基因在研究过的组织。 AcSBP11 AcSBP6 AcSBP4 AcSBP12 四个基因在4°C高表达,而 AcSBP16 在45°C时被上调。通过qRT-PCR验证了某些基因的RNA-Seq。盐胁迫诱导 AcSBP7 AcSBP14 两个基因的表达,而干旱胁迫中 AcSBP12 AcSBP15 的表达em>被高度表达。本研究为菠萝 SBP 基因的进一步基因功能和表达研究奠定了基础。

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