枣椰树(Phoenix dactylifera)主要 RNAi 基因家族的全基因组鉴定和硅学表征。

IF 1.9 Q3 GENETICS & HEREDITY BMC genomic data Pub Date : 2024-03-15 DOI:10.1186/s12863-024-01217-x
Darun Naim, Asif Ahsan, Ahmed Imtiaj, Nurul Haque Mollah
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引用次数: 0

摘要

背景介绍红枣含有多种对健康至关重要的矿物质。主要的 RNA 干扰(RNAi)基因家族通过控制蛋白质编码基因的表达来抵御不同的生物和非生物胁迫,从而在植物的生长和发育过程中发挥重要作用。然而,目前还没有研究枣椰树的这些基因家族。因此,本研究探讨了枣椰树的主要 RNAi 基因及其特征:结果:通过使用 AtRNAi 基因作为 BLASTp 搜索的查询序列,我们从枣椰树基因组中鉴定出了 4 个 PdDCLs、7 个 PdAGOs 和 3 个 PdRDRs 作为 RNAi 蛋白。通过对预测的 RNAi 基因进行结构域分析,发现了与基因沉默机制相关的 Helicase_C、Dicer_dimer、PAZ、RNase III 和 Piwi 结构域。大多数 PdRNAi 蛋白存在于与基因沉默作用相关的细胞核和细胞质中。基因本体(GO)富集分析发现了一些重要的GO术语,包括与蛋白编码基因沉默机制相关的RNA干扰、dsRNA片段化和核糖核酸酶III活性。基因调控网络(GRN)分析发现 PAZ 和 SNF2 是 PdRNAi 基因的转录调控因子。包括Pda-miR156b、Pda-miR396a、Pda-miR166a、Pda-miR167d和Pda-miR529a在内的10个排名靠前的microRNA被鉴定为与不同生物/非生物胁迫相关的PdRNAi基因的关键转录后调控因子。对 PdRNAi 基因的顺式作用调控元件分析发现了一些重要的顺式作用元件,包括 ABRE、MBS、MYB、MYC、Box-4、G-box、I-box 和 STRE,它们与不同的非生物胁迫有关:本研究的结果可能会成为宝贵的资源,通过在湿实验室中的进一步研究,改善枣椰树的不同特性。
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Genome-wide identification and in silico characterization of major RNAi gene families in date palm (Phoenix dactylifera).

Background: Dates contain various minerals that are essential for good health. The major RNA interference (RNAi) gene families play a vital role in plant growth and development by controlling the expression of protein-coding genes against different biotic and abiotic stresses. However, these gene families for date palm are not yet studied. Therefore, this study has explored major RNAi genes and their characteristics in date palm.

Results: We have identified 4 PdDCLs, 7 PdAGOs, and 3 PdRDRs as RNAi proteins from the date palm genome by using AtRNAi genes as query sequences in BLASTp search. Domain analysis of predicted RNAi genes has revealed the Helicase_C, Dicer_dimer, PAZ, RNase III, and Piwi domains that are associated with the gene silencing mechanisms. Most PdRNAi proteins have been found in the nucleus and cytosol associated with the gene silencing actions. The gene ontology (GO) enrichment analysis has revealed some important GO terms including RNA interference, dsRNA fragmentation, and ribonuclease_III activity that are related to the protein-coding gene silencing mechanisms. Gene regulatory network (GRN) analysis has identified PAZ and SNF2 as the transcriptional regulators of PdRNAi genes. Top-ranked 10 microRNAs including Pda-miR156b, Pda-miR396a, Pda-miR166a, Pda-miR167d, and Pda-miR529a have been identified as the key post-transcriptional regulators of PdRNAi genes that are associated with different biotic/abiotic stresses. The cis-acting regulatory element analysis of PdRNAi genes has detected some vital cis-acting elements including ABRE, MBS, MYB, MYC, Box-4, G-box, I-box, and STRE that are linked with different abiotic stresses.

Conclusion: The results of this study might be valuable resources for the improvement of different characteristics in date palm by further studies in wet-lab.

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