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七种经济树种的基因组为多倍体化历史和次生代谢物生物合成提供了见解。

The genomes of seven economic Caesalpinioideae trees provide insights into polyploidization history and secondary metabolite biosynthesis.

机构信息

College of Agronomy, Qingdao Agricultural University, Qingdao 266109, China; Guangdong Laboratory for Lingnan Modern Agriculture (Shenzhen Branch), Genome Analysis Laboratory of the Ministry of Agriculture and Rural Affairs, Agricultural Genomics Institute at Shenzhen, Chinese Academy of Agricultural Sciences, Shenzhen, Guangdong 518120, China.

Guangdong Laboratory for Lingnan Modern Agriculture (Shenzhen Branch), Genome Analysis Laboratory of the Ministry of Agriculture and Rural Affairs, Agricultural Genomics Institute at Shenzhen, Chinese Academy of Agricultural Sciences, Shenzhen, Guangdong 518120, China.

出版信息

Plant Commun. 2024 Sep 9;5(9):100944. doi: 10.1016/j.xplc.2024.100944. Epub 2024 May 10.

DOI:10.1016/j.xplc.2024.100944
PMID:38733080
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11412931/
Abstract

The Caesalpinioideae subfamily contains many well-known trees that are important for economic sustainability and human health, but a lack of genomic resources has hindered their breeding and utilization. Here, we present chromosome-level reference genomes for the two food and industrial trees Gleditsia sinensis (921 Mb) and Biancaea sappan (872 Mb), the three shade and ornamental trees Albizia julibrissin (705 Mb), Delonix regia (580 Mb), and Acacia confusa (566 Mb), and the two pioneer and hedgerow trees Leucaena leucocephala (1338 Mb) and Mimosa bimucronata (641 Mb). Phylogenetic inference shows that the mimosoid clade has a much higher evolutionary rate than the other clades of Caesalpinioideae. Macrosynteny comparison suggests that the fusion and breakage of an unstable chromosome are responsible for the difference in basic chromosome number (13 or 14) for Caesalpinioideae. After an ancient whole-genome duplication (WGD) shared by all Caesalpinioideae species (CWGD, ∼72.0 million years ago [MYA]), there were two recent successive WGD events, LWGD-1 (16.2-19.5 MYA) and LWGD-2 (7.1-9.5 MYA), in L. leucocephala. Thereafter, ∼40% gene loss and genome-size contraction have occurred during the diploidization process in L. leucocephala. To investigate secondary metabolites, we identified all gene copies involved in mimosine metabolism in these species and found that the abundance of mimosine biosynthesis genes in L. leucocephala largely explains its high mimosine production. We also identified the set of all potential genes involved in triterpenoid saponin biosynthesis in G. sinensis, which is more complete than that based on previous transcriptome-derived unigenes. Our results and genomic resources will facilitate biological studies of Caesalpinioideae and promote the utilization of valuable secondary metabolites.

摘要

槐蓝族包含许多对经济可持续性和人类健康至关重要的知名树种,但基因组资源的缺乏阻碍了它们的繁殖和利用。在这里,我们为两种食用和工业树种刺槐(921Mb)和苏木(872Mb),三种遮荫和观赏树种合欢(705Mb)、凤凰木(580Mb)和马占相思(566Mb),以及两种先锋和绿篱树种银合欢(1338Mb)和二色含羞草(641Mb)提供了染色体水平的参考基因组。系统发育推断表明,含羞草类群的进化速度比槐蓝族的其他类群高得多。大片段共线性比较表明,不稳定染色体的融合和断裂是槐蓝族基本染色体数(13 或 14)差异的原因。在所有槐蓝族物种共享的一次古老的全基因组复制(CWGD,约 7200 万年前)之后,银合欢中发生了两次最近的全基因组复制事件,LWGD-1(16.2-19.5 百万年前)和 LWGD-2(7.1-9.5 百万年前)。此后,在银合欢的二倍体化过程中,发生了约 40%的基因丢失和基因组大小收缩。为了研究次生代谢物,我们鉴定了这些物种中参与含羞草素代谢的所有基因拷贝,并发现银合欢中含羞草素生物合成基因的丰度在很大程度上解释了其高含羞草素产量。我们还鉴定了刺槐中参与三萜皂苷生物合成的所有潜在基因,其完整程度超过了基于以前转录组衍生的 unigenes 的结果。我们的结果和基因组资源将促进槐蓝族的生物学研究,并促进有价值的次生代谢物的利用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d92e/11412931/c93eae2d2ed2/gr7.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d92e/11412931/b489ff296abd/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d92e/11412931/ad4173f64242/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d92e/11412931/1a5870ed3fee/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d92e/11412931/0005312b241a/gr4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d92e/11412931/b448f73ce704/gr5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d92e/11412931/d35725715606/gr6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d92e/11412931/c93eae2d2ed2/gr7.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d92e/11412931/b489ff296abd/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d92e/11412931/ad4173f64242/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d92e/11412931/1a5870ed3fee/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d92e/11412931/0005312b241a/gr4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d92e/11412931/b448f73ce704/gr5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d92e/11412931/d35725715606/gr6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d92e/11412931/c93eae2d2ed2/gr7.jpg

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