Abstract Background Although the extreme environmental adaptation of organisms is a hot topic in evolutionary biology, genetic adaptation to high-altitude environment remains poorly characterized in ectothermic animals. Squamates are among the most diverse terrestrial vertebrates, with tremendous ecological plasticity and karyotype diversity, and are a unique model system to investigate the genetic footprints of adaptation. Results We report the first chromosome-level assembly of the Mongolian racerunner ( Eremias argus ) and our comparative genomics analyses found that multiple chromosome fissions/fusions events are unique to lizards. We further sequenced the genomes of 61 Mongolian racerunner individuals that were collected from altitudes ranging from ~ 80 to ~ 2600 m above sea level (m.a.s.l.). Population genomic analyses revealed many novel genomic regions under strong selective sweeps in populations endemic to high altitudes. Genes embedded in those genomic regions are mainly associated with energy metabolism and DNA damage repair pathways. Moreover, we identified and validated two substitutions of PHF14 that may enhance the lizards’ tolerance to hypoxia at high altitudes. Conclusions Our study reveals the molecular mechanism of high-altitude adaptation in ectothermic animal using lizard as a research subject and provides a high-quality lizard genomic resource for future research.
Abstract The survival of ectotherms worldwide is threatened by climate change. Whether increasing temperatures increase the vulnerability of ectotherms inhabiting temperate plateau areas remains unclear. To understand altitudinal variation in the vulnerability of plateau ectotherms to climate warming, Qinghai toad-headed lizards (Phrynocephalus vlangalii) were subjected to semi-natural enclosure experiments with simulated warming at high (2,600 m) and superhigh (3,600 m) elevations of the Dangjin Mountain, China. Our results revealed that the thermoregulatory effectiveness and warming tolerance (WT) of the toad-headed lizards were significantly affected by climate warming at both elevations, but their thermal sensitivity remained unchanged. After warming, the thermoregulatory effectiveness of lizards at superhigh elevations decreased because of the improved environmental thermal quality, whereas that of lizards at high-elevation conditions increased. Although the body temperature selected by high-elevation lizards was also significantly increased, the proportion of their active body temperature falling within the set-point temperature range decreased. This indicates that it is difficult for high-elevation lizards to adjust their body temperatures within a comfortable range under climate warming. Variations in the WT and thermal safety margin (TSM) under climate warming revealed that lizards at the superhigh elevation benefited from improved environmental thermal quality, whereas those at the high elevation originally on the edge of the TSM faced more severe threats and became more vulnerable. Our study highlights the importance of thermal biological traits in evaluating the vulnerability of ectotherms in temperate plateau regions.
Abstract The debate about behavioral thermoregulation inside reptile eggs centers on the frequency (and hence, biological significance) of the phenomenon, not about its validity. Both sides of the debate agree that large eggs in shallow nests laid in sun‐exposed soil will experience clines in mean temperature and (especially) diel thermal variance; that embryos in the middle phase of development have the ability to reposition themselves, and room to do so; and that small changes in developmental temperatures can influence offspring fitness. Equally, all protagonists agree that thermal clines will be too low in some other kinds of nests, and that embryonic repositioning is impossible very early and very late in development. Based on an array of other fitness‐enhancing behaviors exhibited by tetrapod embryos, and general principles for recognizing adaptation, we conclude that behavioral thermoregulation inside the egg likely is adaptive in some but not all reptile species. We identify productive directions for empirical research to resolve points of contention.
Abstract Thickness reduction or loss of the calcareous eggshell is one of major phenotypic changes in the transition from oviparity to viviparity. Whether the reduction of eggshells in viviparous squamates is associated with specific gene losses is unknown. Taking advantage of a newly generated high‐quality genome of the viviparous Chinese crocodile lizard ( Shinisaurus crocodilurus ), we found that ovocleidin‐17 gene ( OC‐17 ), which encodes an eggshell matrix protein that is essential for calcium deposition in eggshells, is not intact in the crocodile lizard genome. Only OC‐17 transcript fragments were found in the oviduct transcriptome, and no OC‐17 peptides were identified in the eggshell proteome of crocodile lizards. In contrast, OC‐17 was present in the eggshells of the oviparous Mongolia racerunner ( Eremias argus ). Although the loss of OC‐17 is not common in viviparous species, viviparous squamates show fewer intact eggshell‐specific proteins than oviparous squamates. Our study implies that functional loss of eggshell‐matrix protein genes may be involved in the reduction of eggshells during the transition from oviparity to viviparity in the crocodile lizard.
Studies of the seasonal acclimatisation of behavioural and physiological processes usually focus on aquatic or semi-aquatic ectotherms and focus less effort on terrestrial ectotherms that experience more thermally heterogeneous environments. We conducted comparative studies and thermal acclimation experiments on the locomotion of the Chinese skink (Plestiodon chinensis) to test whether seasonal acclimatisation in locomotion exists in these terrestrial ectothermic vertebrates, and whether seasonal acclimatisation is predominantly induced by thermal environments. In natural populations, skinks ran faster during the summer season than during the spring season at high-test temperatures ranging from 27°C to 36°C but not at low-test temperatures ranging from 18°C to 24°C. In contrast, the thermal acclimation experiments showed that the cold-acclimated skinks ran faster than the warm-acclimated skinks at the low- test temperatures but not at high-test temperatures. Therefore, the seasonal acclimatisation occurs to P. chinensis, and may be induced by temperature as well as other factors like food availability, as indicated by the seasonal variation in the thermal dependence of locomotion, and the discrepancy between seasonal acclimatisation and thermal acclimation
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