在全基因组范围内鉴定和表征 citrus sinensis (L.) Osbeck 的开花基因:C. Medica L.、C. Reticulata Blanco、C. Grandis (L.) Osbeck 和 C. Clementina 之间的比较。

IF 1.9 Q3 GENETICS & HEREDITY BMC genomic data Pub Date : 2024-02-20 DOI:10.1186/s12863-024-01201-5
Harleen Kaur, Pooja Manchanda, Gurupkar S Sidhu, Parveen Chhuneja
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引用次数: 0

摘要

背景:开花在完成植物生殖周期和获得下一代植物方面起着重要作用。就柑橘而言,可能需要一年多的时间才能获得后代。因此,为了加快育种进程,需要缩短幼苗期。植物的幼苗期受各种开花基因的调控。柑橘的果实和叶片具有多种药用特性,因此需要进行密集的育种计划,以培育出具有更好品质特征的杂交种。为了打破柑橘的幼果期,研究开花基因的作用非常重要。本研究通过基于同源性的方法鉴定了 Citrus sinensis L. Osbeck 的开花调控基因。这些基因的结构和功能特征将有助于针对基因组编辑技术诱导这些基因的突变,从而产生理想的结果:结果:共鉴定出 43 个基因,它们位于柑橘的全部 9 条染色体上。结果:共鉴定出 43 个基因,这些基因位于柑橘的全部 9 条染色体上,并对这些基因的遗传结构、保守基序、顺式调控元件(CREs)和系统发育关系进行了内部分析。共在 33 个基因中检测到 10 个负责开花的 CRE,并在所有基因中发现了 8 个保守基调。通过蛋白质结构、蛋白质相互作用网络和京都基因组百科全书(KEGG)分析,研究了这些基因的功能,发现开花蛋白参与了昼夜节律途径。通过基因本体(GO)和基因功能分析,对基因进行了功能注释。此外,还比较了其他柑橘物种的基因和蛋白质结构,以研究它们之间的进化关系。表达研究揭示了开花基因在花芽和子房中的表达。qRT-PCR分析表明,开花基因在花蕾期、完全成熟的花和果实发育早期均有高表达:结论:研究结果表明,开花基因在柑橘物种中高度保守。qRT-PCR分析揭示了开花基因(CsFT、CsCO、CsSOC、CsAP、CsSEP和CsLFY)的组织特异性表达,这有助于通过各种正向和反向遗传方法轻松检测和定位基因。
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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Genome-wide identification and characterization of flowering genes in Citrus sinensis (L.) Osbeck: a comparison among C. Medica L., C. Reticulata Blanco, C. Grandis (L.) Osbeck and C. Clementina.

Background: Flowering plays an important role in completing the reproductive cycle of plants and obtaining next generation of plants. In case of citrus, it may take more than a year to achieve progeny. Therefore, in order to fasten the breeding processes, the juvenility period needs to be reduced. The juvenility in plants is regulated by set of various flowering genes. The citrus fruit and leaves possess various medicinal properties and are subjected to intensive breeding programs to produce hybrids with improved quality traits. In order to break juvenility in Citrus, it is important to study the role of flowering genes. The present study involved identification of genes regulating flowering in Citrus sinensis L. Osbeck via homology based approach. The structural and functional characterization of these genes would help in targeting genome editing techniques to induce mutations in these genes for producing desirable results.

Results: A total of 43 genes were identified which were located on all the 9 chromosomes of citrus. The in-silico analysis was performed to determine the genetic structure, conserved motifs, cis-regulatory elements (CREs) and phylogenetic relationship of the genes. A total of 10 CREs responsible for flowering were detected in 33 genes and 8 conserved motifs were identified in all the genes. The protein structure, protein-protein interaction network and Kyoto Encyclopedia of Genes and Genomes (KEGG) analysis was performed to study the functioning of these genes which revealed the involvement of flowering proteins in circadian rhythm pathways. The gene ontology (GO) and gene function analysis was performed to functionally annotate the genes. The structure of the genes and proteins were also compared among other Citrus species to study the evolutionary relationship among them. The expression study revealed the expression of flowering genes in floral buds and ovaries. The qRT-PCR analysis revealed that the flowering genes were highly expressed in bud stage, fully grown flower and early stage of fruit development.

Conclusions: The findings suggested that the flowering genes were highly conserved in citrus species. The qRT-PCR analysis revealed the tissue specific expression of flowering genes (CsFT, CsCO, CsSOC, CsAP, CsSEP and CsLFY) which would help in easy detection and targeting of genes through various forward and reverse genetic approaches.

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