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首页> 外文期刊>BMC Plant Biology >Genome-wide identification, gene cloning, subcellular location and expression analysis of SPL gene family in P. granatum L
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Genome-wide identification, gene cloning, subcellular location and expression analysis of SPL gene family in P. granatum L

机译:基因组鉴定,基因克隆,亚细胞位置和P.Granatum L的SPL基因家族的表达分析

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Pomegranate is an excellent tree species with nutritional, medicinal, ornamental and ecological values. Studies have confirmed that SPL factors play an important role in floral transition and flower development. Used bioinformatics methods, 15 SPL (SQUAMOSA promoter-binding protein-like) genes were identified and analyzed from the ‘Taishanhong’ pomegranate (P. granatum L.) genome. Phylogenetic analysis showed that PgSPLs were divided into six subfamilies (G1?~?G6). PgSPL promoter sequences contained multiple cis-acting elements associated with abiotic stress or hormonal response. Based on the transcriptome data, expression profiles of different tissues and different developmental stages showed that PgSPL genes had distinct temporal and spatial expression characteristics. The expression analysis of miR156 in small RNA sequencing results showed that miR156 negatively regulated the expression of target genes. qRT-PCR analysis showed that the expression levels of PgSPL2, PgSPL3, PgSPL6, PgSPL11 and PgSPL14 in leaves were significantly higher than those in buds and stems (p??0.05). The expression levels of PgSPL5, PgSPL12 and PgSPL13 in flower buds were significantly higher than that in leaves and stems (p??0.05). The full-length of coding sequence of PgSPL5 and PgSPL13 were obtained by homologous cloning technology. The full length of PgSPL5 is 1020?bp, and PgSPL13 is 489?bp, which encodes 339 and 162 amino acids, respectively. Further investigation revealed that PgSPL5 and PgSPL13 proteins were located in the nucleus. Exogenous plant growth regulator induction experiments showed that PgSPL5 was up-regulated in leaves and stems. PgSPL13 was up-regulated in leaves and down-regulated in stems. When sprayed with 6-BA, IBA and PP333 respectively, PgSPL5 and PgSPL13 were up-regulated most significantly at P2 (bud vertical diameter was 5.1?~?12.0?mm) stage of bisexual and functional male flowers. Our findings suggested that PgSPL2, PgSPL3, PgSPL6, PgSPL11 and PgSPL14 played roles in leaves development of pomegranate. PgSPL5, PgSPL12 and PgSPL13 played roles in pomegranate flower development. PgSPL5 and PgSPL13 were involved in the response process of different plant hormone signal transduction in pomegranate development. This study provided a robust basis for further functional analyses of SPL genes in pomegranate.
机译:石榴是一种具有营养,药用,观赏和生态价值的优秀树种。研究证实,SPL因子在花卉过渡和花卉开发中发挥着重要作用。用过的生物信息学方法,鉴定了15个SP1(Squamosa启动子结合蛋白质样)基因并从“泰山钟”石榴(P.Granatum L.)基因组分析。系统发育分析表明,PGSPL分为六个亚壳(G1?〜ΔG6)。 PGSPL启动子序列包含与非生物应激或荷尔蒙反应相关的多个顺式作用元件。基于转录组数据,不同组织和不同发育阶段的表达谱表明PGSPL基因具有明显的时间和空间表达特征。 MiR156在小RNA测序结果中的表达分析表明,MiR156负调节靶基因的表达。 QRT-PCR分析表明,叶片中PGSPL2,PGSPL3,PGSPL6,PGSPL11和PGSPL14的表达水平显着高于芽和茎(P≤≤0.05)。花芽中PGSPL5,PGSPL12和PGSPL13的表达水平显着高于叶片和茎(P≤≤0.05)。通过同源克隆技术获得PGSPL5和PGSPL13的全长编码序列。 PGSPL5的全长是1020?BP,PGSPL13分别为489磅,分别编码339和162个氨基酸。进一步的研究表明,PGSPL5和PGSPL13蛋白位于细胞核中。外源性植物生长调节剂诱导实验表明,PGSPL5在叶子和茎中上调。 PGSPL13在叶子中上调,茎中下调。当分别用6-BA,IBA和PP333喷射时,PGSPL5和PGSPL13在P2(芽垂直直径为5.1Ω·〜12.0×12.0毫米)的双性恋和功能性雄花的阶段上升高。我们的研究结果表明,PGSPL2,PGSPL3,PGSPL6,PGSPL11和PGSPL14在石榴叶片开发中发挥作用。 PGSPL5,PGSPL12和PGSPL13在石榴花发育中起作用的作用。 PGSPL5和PGSPL13涉及石榴发育中不同植物激素信号转导的响应过程。本研究为石榴中的SPL基因进行了进一步的功能分析,提供了一种稳健的基础。

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