Yi-Xin Gao
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Research Subjects
Yi-Xin Gao has a total of 11 co-authors. Here are the top co-authors by number of shared publications:
- Dan-Na Yu
College of Life Sciences, Zhejiang Normal University, Jinhua 321004, China
2 shared publications - Hui-Yuan Wu
College of Life Sciences, Zhejiang Normal University, Jinhua 321004, China
2 shared publications - Jia-Yong Zhang
College of Life Sciences, Zhejiang Normal University, Jinhua 321004, China
2 shared publications - Chen-Xiao Hu
College of Life Sciences, Zhejiang Normal University, Jinhua 321004, China
1 shared publication - Chen-Yang Shen
College of Life Sciences, Zhejiang Normal University, Jinhua 321004, China
1 shared publication - Jie-Hong Ji
College of Life Sciences, Zhejiang Normal University, Jinhua 321004, China
1 shared publication
Latest Publications
- Open Access
Comparative Mitogenomics Reveals Gene Rearrangement and Phylogenetic Relationships in Siphlonuroidea (Insecta: Ephemeroptera)
Siphlonuroidea is a superfamily within Ephemeroptera, yet the phylogenetic relationships among its constituent families and their placement relative to other mayfly lineages remain unresolved. To address these questions, we generated and analyzed 16 newly assembled mitochondrial genomes from 14 species across Ephemeroptera, including three species of Ameletidae, four of Siphlonuridae, and nine mitochondrial genomes from seven species of Isonychiidae. Comparative mitogenomic analysis revealed two distinct tRNA gene rearrangement patterns within Siphlonuridae, including trnI-trnQ-trnM-trnQ-trnM-trnQ-trnM-trnQ-trnM and trnI-trnM-trnQ-trnM. In contrast, all Ameletidae mitogenomes share an identical rearrangement of trnI-trnQ-trnM-trnM, which constitutes a potential synapomorphy supporting the monophyly of this family. Compositional analysis further showed that Siphlonuridae and Ameletidae exhibit significantly higher and highly similar A+T contents, clustering together in hierarchical analyses. This characteristic contrasts sharply with Isonychiidae, which displays markedly lower A+T content. Phylogenomic inference based on the PCG12 dataset supports a sister-group relationship between Siphlonuridae and Ameletidae, with this clade itself forming the sister group to a well-supported clade of Isonychiidae and Heptageniidae. Divergence time estimation places the origin of the Ameletidae and Siphlonuridae lineage in the Late Jurassic (174.71 Mya), while Isonychiidae diverged in the Early Cretaceous (136.81 Mya). In conclusion, Siphlonuridae and Ameletidae show a closer affinity and belong to Siphlonuroidea. Isonychiidae shares a closer relationship with Heptageniidae and remains outside Siphlonuroidea. Siphluriscidae is recovered as the sister lineage to all other extant Ephemeroptera, confirming its status as the earliest-diverging extant mayfly lineage.
Open AccessComparative Mitogenomics Reveals Gene Rearrangement and Phylogenetic Relationships in Siphlonuroidea (Insecta: Ephemeroptera)
Siphlonuroidea is a superfamily within Ephemeroptera, yet the phylogenetic relationships among its constituent families and their placement relative to other mayfly lineages remain unresolved. To address these questions, we generated and analyzed 16 newly assembled mitochondrial genomes from 14 species across Ephemeroptera, including three species of Ameletidae, four of Siphlonuridae, and nine mitochondrial genomes from seven species of Isonychiidae. Comparative mitogenomic analysis revealed two distinct tRNA gene rearrangement patterns within Siphlonuridae, including trnI-trnQ-trnM-trnQ-trnM-trnQ-trnM-trnQ-trnM and trnI-trnM-trnQ-trnM. In contrast, all Ameletidae mitogenomes share an identical rearrangement of trnI-trnQ-trnM-trnM, which constitutes a potential synapomorphy supporting the monophyly of this family. Compositional analysis further showed that Siphlonuridae and Ameletidae exhibit significantly higher and highly similar A+T contents, clustering together in hierarchical analyses. This characteristic contrasts sharply with Isonychiidae, which displays markedly lower A+T content. Phylogenomic inference based on the PCG12 dataset supports a sister-group relationship between Siphlonuridae and Ameletidae, with this clade itself forming the sister group to a well-supported clade of Isonychiidae and Heptageniidae. Divergence time estimation places the origin of the Ameletidae and Siphlonuridae lineage in the Late Jurassic (174.71 Mya), while Isonychiidae diverged in the Early Cretaceous (136.81 Mya). In conclusion, Siphlonuridae and Ameletidae show a closer affinity and belong to Siphlonuroidea. Isonychiidae shares a closer relationship with Heptageniidae and remains outside Siphlonuroidea. Siphluriscidae is recovered as the sister lineage to all other extant Ephemeroptera, confirming its status as the earliest-diverging extant mayfly lineage.
- Open Access
Unusual Genetic Diversity Within Thereuopoda clunifera (Wood, 1862) (Chilopoda: Scutigeromorpha) Revealed by Phylogeny and Divergence Times Using Mitochondrial Genomes
As one of the four primary evolutionary groups within myriapods, centipedes (Chilopoda) comprise approximately 3150 valid species. Recent molecular studies have begun to elucidate the phylogeny and time to divergence in Chilopoda; yet, identifying scutigeromorphs at the species level remains a notoriously challenging task. In this study, we obtained seven new complete mitogenomes of Thereuopoda clunifera (Wood, 1862) to investigate the phylogeny and divergence times of Chilopoda. Both maximum likelihood (ML) and Bayesian inference (BI) analyses recovered the relationship of (Scutigeromorpha + (Scolopendromorpha + (Lithobiomorpha + Geophilomorpha))). For Scutigeromorpha, seven newly sequenced mitogenomes of T. clunifera were divided into four distinct clades. Divergence time estimates suggest that the basal split of Chilopoda occurred during the Middle Ordovician period, with the origins of Scolopendromorpha, Lithobiomorpha, and Geophilomorpha dating to the Devonian period. Factors such as warm climates, coevolution between predator and prey, and the rifting of the Hainan Island may have driven the diversification of Scutigeromorpha. Based on genetic distance, the delimitation of molecular species, phylogenetic relationships, and divergence time analyses, we identified three cryptic species that existed within T. clunifera. This exceptionally high degree of hidden diversity can be ascribed to the morphological stasis that has occurred since the Paleozoic era and taxonomic impediment.
Open AccessUnusual Genetic Diversity Within Thereuopoda clunifera (Wood, 1862) (Chilopoda: Scutigeromorpha) Revealed by Phylogeny and Divergence Times Using Mitochondrial Genomes
As one of the four primary evolutionary groups within myriapods, centipedes (Chilopoda) comprise approximately 3150 valid species. Recent molecular studies have begun to elucidate the phylogeny and time to divergence in Chilopoda; yet, identifying scutigeromorphs at the species level remains a notoriously challenging task. In this study, we obtained seven new complete mitogenomes of Thereuopoda clunifera (Wood, 1862) to investigate the phylogeny and divergence times of Chilopoda. Both maximum likelihood (ML) and Bayesian inference (BI) analyses recovered the relationship of (Scutigeromorpha + (Scolopendromorpha + (Lithobiomorpha + Geophilomorpha))). For Scutigeromorpha, seven newly sequenced mitogenomes of T. clunifera were divided into four distinct clades. Divergence time estimates suggest that the basal split of Chilopoda occurred during the Middle Ordovician period, with the origins of Scolopendromorpha, Lithobiomorpha, and Geophilomorpha dating to the Devonian period. Factors such as warm climates, coevolution between predator and prey, and the rifting of the Hainan Island may have driven the diversification of Scutigeromorpha. Based on genetic distance, the delimitation of molecular species, phylogenetic relationships, and divergence time analyses, we identified three cryptic species that existed within T. clunifera. This exceptionally high degree of hidden diversity can be ascribed to the morphological stasis that has occurred since the Paleozoic era and taxonomic impediment.