龙舌兰杂交种 NO.11648 的染色体级基因组组装提供了对 CAM 光合作用的深入了解。

IF 7.6 Q1 GENETICS & HEREDITY 园艺研究(英文) Pub Date : 2023-12-19 eCollection Date: 2024-02-01 DOI:10.1093/hr/uhad269
Ziping Yang, Qian Yang, Qi Liu, Xiaolong Li, Luli Wang, Yanmei Zhang, Zhi Ke, Zhiwei Lu, Huibang Shen, Junfeng Li, Wenzhao Zhou
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引用次数: 0

摘要

姬松茸亚科(Agavoideae)包括茎基酸代谢(CAM)、C3 和 C4 植物,其物种形成的年龄较小,变异积累较慢,因此是研究 CAM 进化的模式作物。然而,由于缺乏基因组信息,CAM进化的遗传机制仍不清楚。本研究利用高通量染色体构象捕获、Nanopore和Illumina技术产生的数据,在染色体水平上组装了龙舌兰杂交种NO.11648的基因组,得到了30条伪染色体,大小为4.87 Gb,支架N50为186.42 Mb。基因组注释发现了 58 841 个蛋白编码基因和 76.91% 的重复序列,其中最主要的重复序列是 I 型重复序列(Copia 和 Gypsy 分别占基因组的 18.34% 和 13.5%)。我们的研究结果还支持在杂交种从天南星亚科(Asparagoideae)分化出来之后,在杂交种的世系中发生了一次全基因组复制事件。此外,我们还发现了磷酸烯醇丙酮酸羧化酶激酶(PEPCK)基因家族的基因复制事件,并揭示了三个 PEPCK 基因(PEPCK3、PEPCK5 和 PEPCK12)参与了 CAM 通路。更重要的是,我们通过分析转录组和使用酵母单杂交实验,确定了富含在昼夜节律、MAPK 信号和植物激素信号通路中调控 PEPCK3 表达的转录因子。我们的研究结果揭示了 CAM 的进化过程,为龙舌兰属植物的分子育种计划提供了重要资源。
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A chromosome-level genome assembly of Agave hybrid NO.11648 provides insights into the CAM photosynthesis.

The subfamily Agavoideae comprises crassulacean acid metabolism (CAM), C3, and C4 plants with a young age of speciation and slower mutation accumulation, making it a model crop for studying CAM evolution. However, the genetic mechanism underlying CAM evolution remains unclear because of lacking genomic information. This study assembled the genome of Agave hybrid NO.11648, a constitutive CAM plant belonging to subfamily Agavoideae, at the chromosome level using data generated from high-throughput chromosome conformation capture, Nanopore, and Illumina techniques, resulting in 30 pseudo-chromosomes with a size of 4.87 Gb and scaffold N50 of 186.42 Mb. The genome annotation revealed 58 841 protein-coding genes and 76.91% repetitive sequences, with the dominant repetitive sequences being the I-type repeats (Copia and Gypsy accounting for 18.34% and 13.5% of the genome, respectively). Our findings also provide support for a whole genome duplication event in the lineage leading to A. hybrid, which occurred after its divergence from subfamily Asparagoideae. Moreover, we identified a gene duplication event in the phosphoenolpyruvate carboxylase kinase (PEPCK) gene family and revealed that three PEPCK genes (PEPCK3, PEPCK5, and PEPCK12) were involved in the CAM pathway. More importantly, we identified transcription factors enriched in the circadian rhythm, MAPK signaling, and plant hormone signal pathway that regulate the PEPCK3 expression by analysing the transcriptome and using yeast one-hybrid assays. Our results shed light on CAM evolution and offer an essential resource for the molecular breeding program of Agave spp.

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