College of Forestry, Fujian Agriculture and Forestry University, Fuzhou, 350002, China.
College of Landscape Architecture, Fujian Agriculture and Forestry University, Fuzhou, 350002, China.
J Integr Plant Biol. 2022 Mar;64(3):649-670. doi: 10.1111/jipb.13217. Epub 2022 Feb 28.
Dendrocalamus latiflorus Munro is a woody clumping bamboo with rapid shoot growth. Both genetic transformation and clustered regularly interspaced short palindromic repeats (CRISPR)/CRISPR-associated protein 9 (Cas9) gene editing techniques are available for D. latiflorus, enabling reverse genetic approaches. Thus, D. latiflorus has the potential to be a model bamboo species. However, the genome sequence of D. latiflorus has remained unreported due to its polyploidy and large genome size. Here, we sequenced the D. latiflorus genome and assembled it into three allele-aware subgenomes (AABBCC), representing the largest genome of a major bamboo species. We assembled 70 allelic chromosomes (2, 737 Mb) for hexaploid D. latiflorus using both single-molecule sequencing from the Pacific Biosciences (PacBio) Sequel platform and chromosome conformation capture sequencing (Hi-C). Repetitive sequences comprised 52.65% of the D. latiflorus genome. We annotated 135 231 protein-coding genes in the genome based on transcriptomes from eight different tissues. Transcriptome sequencing using RNA-Seq and PacBio single-molecule real-time long-read isoform sequencing revealed highly differential alternative splicing (AS) between non-abortive and abortive shoots, suggesting that AS regulates the abortion rate of bamboo shoots. This high-quality hexaploid genome and comprehensive strand-specific transcriptome datasets for this Poaceae family member will pave the way for bamboo research using D. latiflorus as a model species.
巨龙竹是一种丛生的木质竹类,具有快速的笋生长。巨龙竹既可以采用遗传转化技术,也可以采用成簇规律间隔短回文重复序列(CRISPR)/CRISPR 相关蛋白 9(Cas9)基因编辑技术,实现反向遗传学方法。因此,巨龙竹具有成为模式竹种的潜力。然而,由于其多倍体和大基因组大小,巨龙竹的基因组序列仍未被报道。在这里,我们对巨龙竹基因组进行了测序,并将其组装成三个等位基因感知亚基因组(AABBCC),代表了主要竹种中最大的基因组。我们使用来自 Pacific Biosciences(PacBio)Sequel 平台的单分子测序和染色体构象捕获测序(Hi-C),为六倍体巨龙竹组装了 70 个等位染色体(2,737 Mb)。巨龙竹基因组的重复序列占 52.65%。我们基于来自八个不同组织的转录组,在基因组中注释了 135231 个蛋白质编码基因。使用 RNA-Seq 和 PacBio 单分子实时长读 isoform 测序进行的转录组测序揭示了非败育和败育笋之间高度差异的可变剪接(AS),表明 AS 调节竹笋的败育率。这个高质量的六倍体基因组和综合的链特异性转录组数据集将为使用巨龙竹作为模式物种进行竹类研究铺平道路。