Hannon Bozorgmehr Joseph
NECSWS, Manchester, United Kingdom.
J Mol Evol. 2025 Feb;93(1):3-10. doi: 10.1007/s00239-024-10227-3. Epub 2024 Dec 27.
Recently, certain studies have claimed that cognitive features and pathologies unique to humans can be traced to certain changes in the nervous system. These are caused by genes that have likely evolved "from scratch," not having any coding precursors. The translated proteins would not appear outside of the human lineage and any orthologs in other species should be non-coding. This contrasts with research that has identified a decisive role for duplication, and modifications to regulatory sequences, for such phenotypic traits. Closer examination, however, reveals that the inferred lineage-specific emergence of at least two of these genes is likely a misinterpretation owing to a lack of peptide verification, experimental oversights, and insufficient species comparisons. A possible pseudogenic origin is proposed for one of them. The implications of these claims for the study of molecular evolution are discussed.
最近,某些研究声称,人类特有的认知特征和病理现象可追溯到神经系统的某些变化。这些变化是由可能“从头”进化而来的基因引起的,没有任何编码前体。翻译后的蛋白质不会出现在人类谱系之外,其他物种中的任何直系同源物都应该是非编码的。这与已确定基因复制和调控序列修饰对这类表型特征起决定性作用的研究形成了对比。然而,仔细研究发现,由于缺乏肽验证、实验疏忽和物种比较不足,这些基因中至少有两个基因被推断为谱系特异性出现可能是一种误解。其中一个基因被认为可能起源于假基因。本文讨论了这些观点对分子进化研究的影响。