Pereira Andres Barboza, Marano Matthew, Bathala Ramya, Zaragoza Rigoberto Ayala, Neira Andres, Samano Alex, Owoyemi Adekola, Casola Claudio
Interdisciplinary Graduate Program in Genetics & Genomics, Texas A&M University, College Station, Texas, USA.
Interdisciplinary Doctoral Program in Ecology and Evolutionary Biology, Texas A&M University, College Station, Texas, USA.
Bioessays. 2025 Jan;47(1):e2400146. doi: 10.1002/bies.202400146. Epub 2024 Nov 3.
The genome sequencing revolution has revealed that all species possess a large number of unique genes critical for trait variation, adaptation, and evolutionary innovation. One widely used approach to identify such genes consists of detecting protein-coding sequences with no homology in other genomes, termed orphan genes. These genes have been extensively studied, under the assumption that they represent valid proxies for species-specific genes. Here, we critically evaluate taxonomic, phylogenetic, and sequence evolution evidence showing that orphan genes belong to a range of evolutionary ages and thus cannot be assigned to a single lineage. Furthermore, we show that the processes generating orphan genes are substantially more diverse than generally thought and include horizontal gene transfer, transposable element domestication, and overprinting. Thus, orphan genes represent a heterogeneous collection of genes rather than a single biological entity, making them unsuitable as a subject for meaningful investigation of gene evolution and phenotypic innovation.
基因组测序革命揭示,所有物种都拥有大量对性状变异、适应和进化创新至关重要的独特基因。一种广泛用于识别此类基因的方法是检测在其他基因组中没有同源性的蛋白质编码序列,即孤儿基因。这些基因已得到广泛研究,其假设前提是它们代表物种特异性基因的有效代理。在此,我们审慎评估了分类学、系统发育学和序列进化证据,这些证据表明孤儿基因属于一系列进化年龄,因此不能归为单一谱系。此外,我们表明产生孤儿基因的过程比通常认为的要丰富得多,包括水平基因转移、转座元件驯化和重叠基因。因此,孤儿基因代表了一组异质性基因,而非单一生物实体,这使得它们不适合作为有意义的基因进化和表型创新研究对象。