Comparative plastomes of five Psittacanthus species: genome organization, structural features, and patterns of pseudogenization and gene loss.

IF 2.4 3区 生物学 Q2 ECOLOGY
AoB Plants Pub Date : 2025-06-24 eCollection Date: 2025-08-01 DOI:10.1093/aobpla/plaf032
Saddan Morales-Saldaña, Andrea I Barraza-Ochoa, Emanuel Villafán, Antonio Acini Vásquez-Aguilar, Santiago Ramírez-Barahona, Enrique Ibarra-Laclette, Juan Francisco Ornelas
{"title":"Comparative plastomes of five <i>Psittacanthus</i> species: genome organization, structural features, and patterns of pseudogenization and gene loss.","authors":"Saddan Morales-Saldaña, Andrea I Barraza-Ochoa, Emanuel Villafán, Antonio Acini Vásquez-Aguilar, Santiago Ramírez-Barahona, Enrique Ibarra-Laclette, Juan Francisco Ornelas","doi":"10.1093/aobpla/plaf032","DOIUrl":null,"url":null,"abstract":"<p><p>The evolution of heterotrophic lifestyle entails varying degrees of plastome degradation. Yet, the evolutionary trajectory of plastome degradation associated with parasitism remains poorly explored in hemiparasites. We sequenced, assembled, and annotated the complete plastomes of five species of <i>Psittacanthus</i> mistletoes. In addition, publicly available plastomes of 58 species in Loranthaceae were obtained and re-annotated for phylogenetic and comparative analyses. We used a comparative phylogenetic approach to evaluate whether patterns of pseudogenization and gene loss differ among lineages of hemiparasites in Loranthaceae. Gene order was highly conserved, with higher sequence similarity and structural conservation between closely related <i>Psittacanthus</i> species but with considerable plastome size variation (from 121 238 to 125 427 bp). The expansion and contraction at the borders of inverted repeats (IRs) and intergenic regions variation greatly contribute to size variations among <i>Psittacanthus</i> plastomes. Phylogenetic analysis of plastomes of 60 species in Loranthaceae including 5 <i>Psittacanthus</i> species of the previously unsampled tribe Psittacantheae was largely congruent with previous phylogenetic studies. The loss of most of the <i>ndh</i> complex (10 out of 11 genes), <i>rpl32</i>, <i>rps15</i>, and <i>rps16</i> genes, was identified in all studied <i>Psittacanthus</i> species. Also, the loss and pseudogenization of <i>rpl33</i> and <i>rpl36</i> genes in <i>Psittacanthus</i> were uncommon in other Loranthaceae species. The structural variation uncovered in <i>Psittacanthus</i> plastomes reveals that, despite high synteny, significant size variation exists among species. This variation can be attributed to processes such as variations in the length of intergenic regions and the expansion/contraction of IR borders, traits that have been comparatively understudied in earlier Loranthaceae works.</p>","PeriodicalId":48955,"journal":{"name":"AoB Plants","volume":"17 4","pages":"plaf032"},"PeriodicalIF":2.4000,"publicationDate":"2025-06-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12342154/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"AoB Plants","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1093/aobpla/plaf032","RegionNum":3,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/8/1 0:00:00","PubModel":"eCollection","JCR":"Q2","JCRName":"ECOLOGY","Score":null,"Total":0}
引用次数: 0

Abstract

The evolution of heterotrophic lifestyle entails varying degrees of plastome degradation. Yet, the evolutionary trajectory of plastome degradation associated with parasitism remains poorly explored in hemiparasites. We sequenced, assembled, and annotated the complete plastomes of five species of Psittacanthus mistletoes. In addition, publicly available plastomes of 58 species in Loranthaceae were obtained and re-annotated for phylogenetic and comparative analyses. We used a comparative phylogenetic approach to evaluate whether patterns of pseudogenization and gene loss differ among lineages of hemiparasites in Loranthaceae. Gene order was highly conserved, with higher sequence similarity and structural conservation between closely related Psittacanthus species but with considerable plastome size variation (from 121 238 to 125 427 bp). The expansion and contraction at the borders of inverted repeats (IRs) and intergenic regions variation greatly contribute to size variations among Psittacanthus plastomes. Phylogenetic analysis of plastomes of 60 species in Loranthaceae including 5 Psittacanthus species of the previously unsampled tribe Psittacantheae was largely congruent with previous phylogenetic studies. The loss of most of the ndh complex (10 out of 11 genes), rpl32, rps15, and rps16 genes, was identified in all studied Psittacanthus species. Also, the loss and pseudogenization of rpl33 and rpl36 genes in Psittacanthus were uncommon in other Loranthaceae species. The structural variation uncovered in Psittacanthus plastomes reveals that, despite high synteny, significant size variation exists among species. This variation can be attributed to processes such as variations in the length of intergenic regions and the expansion/contraction of IR borders, traits that have been comparatively understudied in earlier Loranthaceae works.

五种鹦鹉螺的质体比较:基因组组织、结构特征、假原化和基因丢失模式。
异养生活方式的进化需要不同程度的质体降解。然而,在半寄生虫中,与寄生相关的质体降解的进化轨迹仍然很少被探索。我们对五种槲寄生进行了完整的质体测序、组装和注释。此外,我们还获得了58种Loranthaceae植物的质体,并对其进行了系统发育和比较分析。我们使用比较系统发育的方法来评估是否假变性和基因丢失的模式不同谱系的半寄生在罗兰科。基因序列高度保守,亲缘关系较近的鹦鹉科物种间具有较高的序列相似性和结构保守性,但质体大小差异较大(从121238 ~ 124527 bp)。倒置重复序列(IRs)边缘的扩张和收缩以及基因间区域的变异是鹦鹉体质粒大小差异的重要原因。对Loranthaceae 60种植物质体的系统发育分析,包括先前未采样的Psittacantheae部落的5种Psittacantheae,与以往的系统发育研究基本一致。11个基因中有10个缺失了大部分的ndh复合物,即rpl32、rps15和rps16基因。此外,rpl33和rpl36基因在鹦鹉螺科其他物种中也不常见。在鹦鹉体质体中发现的结构变异表明,尽管具有高度的同质性,但物种之间存在显著的大小差异。这种变异可以归因于基因间区域长度的变化和IR边界的扩张/收缩等过程,这些特征在早期的Loranthaceae研究中相对较少。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
AoB Plants
AoB Plants PLANT SCIENCES-
CiteScore
4.80
自引率
0.00%
发文量
54
审稿时长
20 weeks
期刊介绍: AoB PLANTS is an open-access, online journal that has been publishing peer-reviewed articles since 2010, with an emphasis on all aspects of environmental and evolutionary plant biology. Published by Oxford University Press, this journal is dedicated to rapid publication of research articles, reviews, commentaries and short communications. The taxonomic scope of the journal spans the full gamut of vascular and non-vascular plants, as well as other taxa that impact these organisms. AoB PLANTS provides a fast-track pathway for publishing high-quality research in an open-access environment, where papers are available online to anyone, anywhere free of charge.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信