Biology and Evolution of Marine Organisms, Stazione Zoologica Anton Dohrn, Napoli 80121, Italy.
Laboratory for Evolutionary Morphology, RIKEN Center for Biosystems Dynamics Research (BDR), Kobe 650-0047, Japan.
Proc Biol Sci. 2022 Aug 10;289(1980):20220667. doi: 10.1098/rspb.2022.0667.
Nitric oxide (NO) is an ancestral key signalling molecule essential for life and has enormous versatility in biological systems, including cardiovascular homeostasis, neurotransmission and immunity. Although our knowledge of NO synthases (Nos), the enzymes that synthesize NO , is substantial, the origin of a large and diversified repertoire of gene orthologues in fishes with respect to tetrapods remains a puzzle. The recent identification of in the ray-finned fish spotted gar, which was considered lost in this lineage, changed this perspective. This finding prompted us to explore gene evolution, surveying vertebrate species representing key evolutionary nodes. This study provides noteworthy findings: first, experienced several lineage-specific gene duplications and losses. Second, was found to be lost independently in two different teleost lineages, Elopomorpha and Clupeocephala. Third, the expression of at least one paralogue in the gills of developing shark, bichir, sturgeon, and gar, but not in lamprey, suggests that expression in this organ may have arisen in the last common ancestor of gnathostomes. These results provide a framework for continuing research on genes' roles, highlighting subfunctionalization and reciprocal loss of function that occurred in different lineages during vertebrate genome duplications.
一氧化氮(NO)是一种古老的关键信号分子,对生命至关重要,在包括心血管稳态、神经递质传递和免疫在内的生物系统中具有巨大的多功能性。尽管我们对合成 NO 的酶——一氧化氮合酶(Nos)有了相当的了解,但鱼类与四足动物相比,其大量多样化的基因直系同源物的起源仍然是一个谜。最近在射线鳍鱼类斑点叉尾鮰中发现了它,这改变了这一看法,而在该谱系中,人们曾认为它已经丢失。这一发现促使我们探索基因的进化,调查了代表关键进化节点的脊椎动物物种。这项研究提供了值得注意的发现:首先,经历了几次谱系特异性的基因重复和丢失。其次,发现它在两个不同的硬骨鱼谱系(Elopomorpha 和 Clupeocephala)中独立丢失。第三,在鲨鱼、比目鱼、鲟鱼和叉尾鮰的鳃中至少有一种 基因的一个旁系同源物的表达,但在七鳃鳗中没有,这表明在有颌类的共同祖先中,该器官中的 表达可能已经出现。这些结果为继续研究 基因的作用提供了一个框架,强调了在脊椎动物基因组加倍过程中不同谱系中发生的亚功能化和功能相互丧失。