Transcriptome Analysis of Self- and Cross-pollinated Pistils of Japanese Apricot (Prunus mume Sieb. et Zucc.)

T. Habu, R. Tao
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引用次数: 15

Abstract

Solanaceae, Rosaceae, and Plantaginaceae exhibit the S-RNase-based gametophytic self-incompatibility (GSI) system. This type of GSI is controlled by a single polymorphic locus ( S locus) containing the pistil S determinant gene, S-ribonuclease ( S-RNase ), and the pollen S determinant, the S locus F-box gene ( SFB/SLF ). In addition to these determinant genes, non-S factors, called modifier genes, are required for the GSI reaction. Here, we conducted large-scale transcriptome analysis of unpollinated, self-pollinated, and cross-pollinated pistils of Japanese apricot ( Prunus mume Sieb. et Zucc. cv. Nanko) to capture all of the molecular events induced by the GSI reaction in Prunus , using next-generation sequencing technologies. We obtained 40,061 unigenes from 77,521,310 reads from pollinated and unpollinated pistils and pollen grains. Among these unigenes, 29,985 and 27,898 unigene sequences showed at least one hit against the NCBI nr and TAIR10 protein databases, respective - ly, in BLASTX searches using an E-value cutoff of 1e-6. Digital expression analysis showed that 8,907 and 10,190 unigenes were expressed at significantly different levels between unpollinated (UP) and cross-pollinated (CP) pistils and between UP and self-pollinated (SP) pistils, respectively. The expression of 4,348 unigenes in both CP and SP pollination was commonly and significantly different from that in UP, while the expression of 4,559 and 5,842 unigenes in CP and SP, respectively, was specifically and significantly different from UP. The expression of 2,227 unigenes was up-regulated both in CP and SP compared with UP. Genes supposedly involved in S-RNase-based GSI were included among the unigenes up-regulated by pollination, while no unigenes homologous to the solanaceous pistil modifiers HT-B or 120K were included among the unigenes up-regulated by pollination or in the whole unpollinated/pollinated pistil transcriptome. We discuss the distinct molecular mechanism of S-RNase-based GSI in Prunus .
日本杏自花授粉和异花授粉雌蕊转录组分析。调查)。
茄科、蔷薇科和车前草科均具有基于s - rase的配子体自交不亲和(GSI)系统。这种类型的GSI由单个多态性位点(S位点)控制,该位点包含雌蕊S-核糖核酸酶(S- rnase)决定基因和花粉S决定基因S位点F-box基因(SFB/SLF)。除了这些决定基因外,GSI反应还需要非s因子,称为修饰基因。在此,我们对日本杏(Prunus mume Sieb)的未授粉、自花授粉和异花授粉雌蕊进行了大规模的转录组分析。调查。简历。Nanko)利用下一代测序技术捕获了Prunus中GSI反应诱导的所有分子事件。我们从授粉和未授粉的雌蕊和花粉粒的77,521,310个reads中获得了40,061个unique genes。在这些单基因序列中,29,985和27,898个单基因序列在BLASTX中分别与NCBI nr和TAIR10蛋白数据库至少有一个匹配,使用e值截断值为1e-6。数字表达分析显示,在未授粉雌蕊(UP)和异花授粉雌蕊(CP)以及UP与自花授粉雌蕊(SP)之间,分别有8907个和10190个unigenes的表达量显著不同。在CP和SP授粉中,有4348个基因的表达与UP有显著性共性差异,而CP和SP授粉中分别有4559个和5842个基因的表达与UP有显著性特异性差异。与UP相比,CP和SP中有2227个基因表达上调。据推测与s - rase基GSI相关的基因在传粉上调的单基因中被发现,而在传粉上调的单基因中或在整个未授粉/授粉雌蕊转录组中均未发现与向日葵雌蕊修饰子HT-B或120K同源的单基因。我们讨论了李树s - rase基GSI的独特分子机制。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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