黑麦(Secale cereale L.)中的磷酸盐转运体(Pht)基因家族--全基因组鉴定和序列多样性评估

David Chan-Rodriguez, Bian Wakimwayi Koboyi, Sirine Werghi, Bradley J Till, Julia Maksymiuk, Fatemeh Shoormij, Abuya Hilderlith, Anna Hawliczek, Maksymilian Krolik, Hanna Bolibok-Bragoszewska
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引用次数: 0

摘要

背景:磷是植物生长和发育不可或缺的重要营养元素。植物利用专门的转运体(PHT)吸收无机磷并将其分配到整个植株。PHT 转运体分为五个家族:PHT1 至 PHT5。每个 PHT 家族都有特定的生理和细胞功能。黑麦(Secale cereale L.)属于三尖杉科,是小麦育种的重要变异来源。它被认为是 Triticeae(三叶草科)中对营养缺乏耐受性最高的植物。迄今为止,还没有关于黑麦缺磷反应基因的报道。本研究的目的是:(i) 鉴定黑麦中不同磷酸盐转运体家族的推定成员并确定其特征;(i) 通过低覆盖率重测序(DArTreseq)评估其在不同黑麦品种中的序列多样性;(iii) 评估推定的黑麦 Pht 基因在磷酸盐缺乏条件下的表达情况:结果:我们在黑麦 Lo7 和 Weining 参考基因组中分别发现了 29 和 35 个推定 Pht 转运体基因,代表了所有已知的 Pht 家族。系统进化分析表明,黑麦 PHT 与其他物种中先前表征的 PHT 蛋白关系密切。对在缺π和对照条件下生长的 Lo7 植株的叶片和根样本进行的定量 RT PCR 表明,ScPht1;6、ScPht2 和 ScPht3;1 对缺π具有响应性。基于对 94 个不同黑麦品种的 DArTreseq 基因分型,我们在黑麦 ScPht 中发现了 820 个多态位点,其中包括 12 个可能具有有害影响的变体。不同 ScPht 基因间的 SNP 密度差异显著:本报告是阐明黑麦对π缺乏反应机制的第一步。我们的研究结果表明,从基因拷贝数变异到 Pht 家族成员之间多态性水平的差异,黑麦对当地环境的适应存在多个层面。DArTreseq 基因分型技术可以快速、经济地评估各基因/基因家族的多态性水平,并支持识别和优先选择候选基因进行进一步研究。总之,我们的研究结果为选择最有希望的候选基因进行进一步功能表征奠定了基础。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Phosphate transporter (Pht) gene families in rye (Secale cereale L.) – genome-wide identification and sequence diversity assessment
Background: Phosphorus is a macronutrient indispensable for plant growth and development. Plants utilize specialized transporters (PHT) to take up inorganic phosphorus and distribute it throughout the plant. The PHT transporters are divided into five families: PHT1 to PHT5. Each PHT family has a particular physiological and cellular function. Rye (Secale cereale L.) is a member of Triticeae, and an important source of variation for wheat breeding. It is considered to have the highest tolerance of nutrient deficiency, among Triticeae. To date, there is no report about genes involved in response to phosphorus deficiency in rye. The aim of this study was to: (i) identify and characterize putative members of different phosphate transporter families in rye, (i) assess their sequence diversity in a collection of diverse rye accessions via low-coverage resequencing (DArTreseq), and (iii) evaluate the expression of putative rye Pht genes under phosphate-deficient conditions. Results: We identified 29 and 35 putative Pht transporter genes in the rye Lo7 and Weining reference genomes, respectively, representing all known Pht families. Phylogenetic analysis revealed a close relationship of rye PHT with previously characterized PHT proteins from other species. Quantitative RT PCR carried out on leaf and root samples of Lo7 plants grown in Pi-deficient and control condition demonstrated that ScPht1;6, ScPht2 and ScPht3;1 are Pi-deficiency responsive. Based on DArTreseq genotyping of 94 diverse rye accessions we identified 820 polymorphic sites within rye ScPht, including 12 variants with a putatively deleterious effect. SNP density varied markedly between ScPht genes. Conclusions: This report is the first step toward elucidating the mechanisms of rye response to Pi deficiency. Our findings point to multiple layers of adaptation to local environments, ranging from gene copy number variation to differences in level of polymorphism across Pht family members. DArTreseq genotyping permits for a quick and cost-effective assessment of polymorphism levels across genes/gene families and supports identification and prioritization of candidates for further studies. Collectively our findings provide the foundation for selecting most promising candidates for further functional characterization.
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