Wang Ruan-Lin, Liu Xiao-Yan, Meng Qing-Yao, Zhang Xin, Fu Yue-Jun, Liang Ai-Hua
Key Laboratory of Chemical Biology and Molecular Engineering of Ministry of Education, Institute of Biotechnology, Shanxi University, Taiyuan, 030006, China.
Shanxi Key Laboratory of Biotechnology, Taiyuan, 030006, China.
BMC Genomics. 2025 Jul 19;26(1):676. doi: 10.1186/s12864-025-11870-w.
Programmed ribosome frameshifting is a translational recoding event in which ribosomes slip forward or backward along the mRNA. Although genes utilizing programmed ribosomal frameshifting for their expression have been found in most organisms, such genes are commonly considered rare. However, previous studies indicated that both +1 and +2 ribosomal frameshifting are frequently required for the expression of genes in the ciliates Euplotes. In this study, we explored the possible evolutionary origin of the frameshift sites by comparative transcriptome and genome analyses.
We sequenced the transcriptomes of different Euplotes octocarinatus strains and performed comparative analyses of the frameshift sites. Finally, a total of 147 non-conserved frameshift sites among different strains were identified. Multiple sequence alignment results showed that +1 frameshift sites could be generated by random single-nucleotide insertion and +2 frameshift sites could be generated by insertion of 'TA' or single-nucleotide deletion. In addition, frameshift sites tend to be less frequent in highly expressed genes. The distances between indel sites and frameshift sites were generally short. And the changed amino acids numbers of the indel sites located inside the protein domain were significantly less than that of the indel sites located outside the domain. Furthermore, we also found a putatively newly formed frameshift site which exists only in the macronucleus but not in the micronucleus of Euplotes woodruffi.
We provide an overview of the evolutionary origin of frameshift sites in Euplotes. Our results suggest that the widespread ribosomal frameshifting in Euplotes may be a result of long-term accumulation of indel mutation. And preservation of these indel mutations in the genome of Euplotes apparently need to meet some constraints.
程序性核糖体移码是一种翻译重编码事件,其中核糖体沿着mRNA向前或向后滑动。尽管在大多数生物体中都发现了利用程序性核糖体移码进行表达的基因,但这类基因通常被认为是罕见的。然而,先前的研究表明,在纤毛虫游仆虫中,基因表达经常需要 +1 和 +2 核糖体移码。在本研究中,我们通过比较转录组和基因组分析探索了移码位点可能的进化起源。
我们对不同八肋游仆虫菌株的转录组进行了测序,并对移码位点进行了比较分析。最终,在不同菌株中鉴定出了总共147个非保守移码位点。多序列比对结果表明,+1 移码位点可由随机单核苷酸插入产生,+2 移码位点可由“TA”插入或单核苷酸缺失产生。此外,移码位点在高表达基因中往往出现频率较低。插入缺失位点与移码位点之间的距离通常较短。并且位于蛋白质结构域内部的插入缺失位点的氨基酸变化数量明显少于位于结构域外部的插入缺失位点。此外,我们还发现了一个推测新形成的移码位点,它仅存在于伍氏游仆虫的大核中,而不存在于小核中。
我们概述了游仆虫中移码位点的进化起源。我们的结果表明,游仆虫中广泛存在的核糖体移码可能是插入缺失突变长期积累的结果。并且这些插入缺失突变在游仆虫基因组中的保留显然需要满足一些限制条件。