Qin Tian, Han Jie, Fan Chunmei, Sun Heng, Rauf Naveed, Wang Tingzhang, Yin Zi, Chen Xiao
Department of Orthopedic Surgery of Sir Run Run Shaw Hospital, and Liangzhu Laboratory, Zhejiang University School of Medicine, Hangzhou, China.
Dr. Li Dak Sum & Yip Yio Chin Center for Stem Cells and Regenerative Medicine, Zhejiang University School of Medicine, Hangzhou, China.
Comput Struct Biotechnol J. 2024 Aug 21;23:3186-3198. doi: 10.1016/j.csbj.2024.08.014. eCollection 2024 Dec.
Axolotls are known for their remarkable regeneration ability. Exploring their transcriptome provides insight into regenerative mechanisms. However, the current annotation of the axolotl transcriptome is limited, leaving the role of unannotated transcripts in regeneration unknown. To discourse this challenge, we exploited long-read sequencing technology, which enables direct observation of full-length RNA transcripts, greatly enhancing the coverage and accuracy of axolotl transcriptome annotation. By utilizing this method, we identified 222 novel gene loci and 4775 novel transcripts, which were quantified using short-read sequencing data. Through the inclusive analysis, we discovered novel homologs, potential functional proteins, noncoding RNAs, and alternative splicing events in key regeneration pathways. In particular, we identified novel transcripts with high protein-coding potential implicated in cell cycle regulation and musculoskeletal development, and regeneration were identified. Interestingly, alternative splice variants were also detected across diverse pathways critical to regeneration. This specifies that these novel transcripts potentially play vital roles underpinning the robust regenerative capacities of axolotls. Single-cell transcriptomic analysis further revealed these isoforms to predominantly exist in axolotl limb chondrocytes and mature tissue cell populations. Overall, the findings significantly advanced consideration of the axolotl transcriptome and provided a new perspective for understanding the mechanisms of regenerative abilities of axolotls.
美西螈以其卓越的再生能力而闻名。对其转录组进行探索有助于深入了解再生机制。然而,目前美西螈转录组的注释有限,使得未注释转录本在再生中的作用尚不清楚。为应对这一挑战,我们采用了长读长测序技术,该技术能够直接观察全长RNA转录本,极大地提高了美西螈转录组注释的覆盖范围和准确性。通过使用这种方法,我们鉴定出222个新基因位点和4775个新转录本,并利用短读长测序数据对它们进行了定量分析。通过全面分析,我们在关键再生途径中发现了新的同源物、潜在功能蛋白、非编码RNA和可变剪接事件。特别是,我们鉴定出了具有高蛋白编码潜力且与细胞周期调控和肌肉骨骼发育相关的新转录本,并确定了它们在再生中的作用。有趣的是,在对再生至关重要的各种途径中也检测到了可变剪接变体。这表明这些新转录本可能在支撑美西螈强大再生能力方面发挥着至关重要的作用。单细胞转录组分析进一步揭示,这些异构体主要存在于美西螈肢体软骨细胞和成熟组织细胞群体中。总体而言,这些发现显著推进了对美西螈转录组的认识,并为理解美西螈再生能力的机制提供了新的视角。