Identification of S-locus F-box Protein Sequences in Diploid Potato, Solanum okadae, via Degenerate PCR.

IF 1 Q3 BIOLOGY
Amar Hundare
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引用次数: 0

Abstract

In many plant species, self-incompatibility (SI) is a mechanism that inhibits inbreeding. SI is gametophytic in the Solanaceae, with specificity determined by S-ribonucleases (S-RNases) in the pistil and S-locus F-box proteins (SLFs) in the pollen. The role of these proteins has been studied extensively in the Solanaceae, often using Petunia as a model. Using degenerate PCR and Sanger sequencing, this protocol identified three SLF sequences from self-incompatible diploid potato (Solanum okadae). While SLFs are well-characterized in model species like Petunia, there is limited sequence data and no standardized protocols for identifying SLFs in non-model species such as S. okadae, hindering broader insights into SI across the Solanaceae. This protocol fills that gap by using degenerate PCR and Sanger sequencing with primers designed from conserved Petunia SLF regions to identify SLF sequences in S. okadae. SLF sequences from 10 distinct Solanaceae members sharing maximum identity with the S2-haplotype of Petunia were used to design two pairs of primers targeting different regions of the target sequence. PCR amplification using designed degenerate primers yielded amplicons that were directly sequenced and joined together to get the partial SLF sequence. It was observed that the S. okadae shared an orthologous relation with the Petunia SLF according to the phylogenetic analysis. These SLFs could be used in future SI breakdown experiments via the competitive interaction route. This protocol, including the primer design, is novel for detecting SLF sequences in S. okadae. Key features • This protocol is applicable when the exact nucleotide sequence of the target DNA is not known but can be deduced from an amino acid sequence. • Straightforward, cost-effective, and can be used to find "new" genes or gene families. • Guidelines and a systematic approach for designing degenerate primers, along with a framework for annotating and comparing SLF genes within the Solanaceae family.

二倍体冈田茄s -座F-box蛋白序列的退化PCR鉴定
在许多植物物种中,自交不亲和(SI)是抑制近亲繁殖的一种机制。SI是茄科植物的配子体,其特异性由雌蕊中的s -核糖核酸酶(S-RNases)和花粉中的s -位点F-box蛋白(SLFs)决定。这些蛋白在茄科植物中的作用已被广泛研究,通常以牵牛花为模型。利用退化PCR和Sanger测序技术,鉴定了自交不亲和二倍体马铃薯(Solanum okadae)的三个SLF序列。虽然slf在矮牵牛等模式物种中有很好的特征,但序列数据有限,并且没有标准化的协议来识别非模式物种(如S. okadae)的slf,这阻碍了对茄科SI的更广泛了解。该方案填补了这一空白,利用退化PCR和Sanger测序,从保守的矮牵牛花SLF区域设计引物,以鉴定S. okadae的SLF序列。利用与矮牵牛s2单倍型最大同源性的10个茄科植物SLF序列,设计了针对目标序列不同区域的两对引物。利用设计的退化引物进行PCR扩增,得到的扩增子直接测序并连接在一起,得到部分SLF序列。系统发育分析表明,冈田花与矮牵牛SLF具有同源关系。这些slf可以通过竞争相互作用途径用于未来的SI击穿实验。该方案,包括引物设计,是一种检测冈田花SLF序列的新方法。•当目标DNA的确切核苷酸序列不知道,但可以从氨基酸序列推断时,此方案适用。•简单,成本效益高,可用于寻找“新”基因或基因家族。•设计退化引物的指南和系统方法,以及用于注释和比较茄科SLF基因的框架。
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CiteScore
1.50
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