先驱型红树总形紫杉的高质量基因组解释了其在潮间带再造林中的优势。

IF 5.5 1区 生物学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY
Ranran Zhu, Shao Shao, Wei Xie, Zixiao Guo, Ziwen He, Yulong Li, Wenqing Wang, Cairong Zhong, Suhua Shi, Shaohua Xu
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引用次数: 0

摘要

红树林生态系统易受近期生境扰动的影响,其生态恢复对热带海岸保护至关重要。摘要总形红树(Laguncularia racemosa)是大西洋东太平洋(AEP)地区潮间带环境中的先锋树种,在中国已被用于植树造林。然而,其快速生长和高适应潜力的分子机制尚不清楚。通过PacBio单分子实时测序,我们完成了高质量的总状乳杆菌基因组组装,全长1105 Mb,支架N50为3.46 Mb。基因组系统发育表明,总状乳杆菌在全球变暖时期侵入潮间带。总状藓与3个本地优势红树林枝的多水平基因组趋同分析表明,它们在营养吸收和高耐盐基因上发生了趋同变化。这也许可以解释总状乳杆菌在引进后对潮间带环境的适应。没有最近的全基因组复制或激活的转座元件,总状乳杆菌保留了许多串联基因复制。其中一些基因参与生长素的生物合成、强光胁迫和冷胁迫响应途径,与总状菌在强光或低温条件下快速生长的能力有关。总之,我们的研究确定了潮间带环境适应的共同机制和红树林在不利条件下快速生长的独特遗传变化,并揭示了白红树林在生态恢复中的作用的分子机制。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
High-quality genome of a pioneer mangrove Laguncularia racemosa explains its advantages for intertidal zone reforestation.

Ecological restoration of mangrove ecosystems that became susceptible to recent habitat perturbations is crucial for tropical coast conservation. The white mangrove Laguncularia racemosa, a pioneer species inhabiting intertidal environments of the Atlantic East Pacific (AEP) region, has been used for reforestation in China for decades. However, the molecular mechanisms underlying its fast growth and high adaptive potential remain unknown. Using PacBio single-molecule real-time sequencing, we completed a high-quality L. racemosa genome assembly covering 1105 Mb with scaffold N50 of 3.46 Mb. Genomic phylogeny shows that L. racemosa invaded intertidal zones during a period of global warming. Multi-level genomic convergence analyses between L. racemosa and three native dominant mangrove clades show that they experienced convergent changes in genes involved in nutrient absorption and high salinity tolerance. This may explain successful L. racemosa adaptation to stressful intertidal environments after introduction. Without recent whole-genome duplications or activated transposable elements, L. racemosa has retained many tandem gene duplications. Some of them are involved in auxin biosynthesis, intense light stress and cold stress response pathways, associated with L. racemosa's ability to grow fast under high light or cold conditions when used for reforestation. In summary, our study identifies shared mechanisms of intertidal environmental adaptation and unique genetic changes underlying fast growth in mangrove-unfavourable conditions and sheds light on the molecular mechanisms of the white mangrove utility in ecological restoration.

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来源期刊
Molecular Ecology Resources
Molecular Ecology Resources 生物-进化生物学
CiteScore
15.60
自引率
5.20%
发文量
170
审稿时长
3 months
期刊介绍: Molecular Ecology Resources promotes the creation of comprehensive resources for the scientific community, encompassing computer programs, statistical and molecular advancements, and a diverse array of molecular tools. Serving as a conduit for disseminating these resources, the journal targets a broad audience of researchers in the fields of evolution, ecology, and conservation. Articles in Molecular Ecology Resources are crafted to support investigations tackling significant questions within these disciplines. In addition to original resource articles, Molecular Ecology Resources features Reviews, Opinions, and Comments relevant to the field. The journal also periodically releases Special Issues focusing on resource development within specific areas.
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