Volume 42 Issue 6
Nov.  2021
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Kai He, Xing Chen, Yin-Bin Qiu, Zhu Liu, Wen-Zhi Wang, Neal Woodman, Jesús E. Maldonado, Xinghua Pan. Mitogenome and phylogenetic analyses support rapid diversification among species groups of small-eared shrews genus Cryptotis (Mammalia: Eulipotyphla: Soricidae). Zoological Research, 2021, 42(6): 739-745. doi: 10.24272/j.issn.2095-8137.2021.199
Citation: Kai He, Xing Chen, Yin-Bin Qiu, Zhu Liu, Wen-Zhi Wang, Neal Woodman, Jesús E. Maldonado, Xinghua Pan. Mitogenome and phylogenetic analyses support rapid diversification among species groups of small-eared shrews genus Cryptotis (Mammalia: Eulipotyphla: Soricidae). Zoological Research, 2021, 42(6): 739-745. doi: 10.24272/j.issn.2095-8137.2021.199

Mitogenome and phylogenetic analyses support rapid diversification among species groups of small-eared shrews genus Cryptotis (Mammalia: Eulipotyphla: Soricidae)

doi: 10.24272/j.issn.2095-8137.2021.199
Funds:  This work was supported by the National Natural Science Foundation of China (31970389 to K.H., 81770173 to X.P.) China Postdoctoral Science Foundation (2009M652952 to K.H.), and Pearl River Talents Program Local Innovative and Research Teams (2017BT01S131 to X.P.)
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  • Corresponding author: E-mail: hekai2018@smu.edupanvictor@qq.com
  • Received Date: 2021-08-08
  • Accepted Date: 2021-10-08
  • Published Online: 2021-10-09
  • Publish Date: 2021-11-18
  • The small-eared shrew genus Cryptotis is the third largest in the family Soricidae and occurs in North, Central, and northern South America. In Mexico and Central and South America, most species inhabit geographically isolated moist, montane habitats at middle and high elevations in a typical sky-island pattern. The 49 recognized species have been partitioned into as many as six species groups based on morphological and molecular phylogenetic studies. The relationships among these species groups are poorly resolved, and their evolutionary histories, including migration patterns and locomotor adaptations, remain unclear. Herein, we provide a new phylogeny incorporating complete mitochondrial genomes (mitogenomes) and supermatrix approach. We compared different evolutionary scenarios using approximately unbiased (AU), Kishino-Hasegawa (KH), and Shimodaira-Hasegawa (SH) statistical tests. The phylogenetic hypothesis based on mitogenomes revealed novel relationships supporting a basal position for the Cryptotis parvus-group in the genus, and a close relationship between C. gracilis and one clade of the C. thomasi-group. The former relationship is consistent with the least derived humerus morphology and northern distribution of the species. The latter relationship implies multiple migrations between Central and South America. The lack of fine resolution for the species group relationships may be due partly to the lack of taxon sampling. In contrast, multi-approach analyses suggest that the unresolved relationships may be a result of rapid diversification during the early stages of Cryptotis evolution.
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  • [1]
    Andermann T, Torres Jiménez MF, Matos-Maraví P, Batista R, Blanco-Pastor JL, Gustafsson ALS, et al. 2020. A guide to carrying out a phylogenomic target sequence capture project. Frontiers in Genetics, 10: 1407. doi: 10.3389/fgene.2019.01407
    [2]
    Andrews S. 2010. FastQC: a quality control tool for high throughput sequence data. Babraham Bioinformatics, Babraham Institute, Cambridge, United Kingdom.
    [3]
    Baird AB, McCarthy TJ, Trujillo RG, Kang YY, Esmaeiliyan M, Valdez J, et al. 2018. Molecular systematics and biodiversity of the Cryptotis mexicanus group (Eulipotyphla: Soricidae): two new species from Honduras supported. Systematics and Biodiversity, 16(2): 108−117.
    [4]
    Baker RH, Desalle R. 1997. Multiple sources of character information and the phylogeny of Hawaiian drosophilids. Systematic Biology, 46(4): 654−673.
    [5]
    Bolger AM, Lohse M, Usadel B. 2014. Trimmomatic: a flexible trimmer for Illumina sequence data. Bioinformatics, 30(15): 2114−2120.
    [6]
    Bouckaert R, Heled J, Kühnert D, Vaughan T, Wu CH, Xie D, et al. 2014. BEAST 2: a software platform for Bayesian evolutionary analysis. PLoS Computational Biology, 10(4): e1003537. doi: 10.1371/journal.pcbi.1003537
    [7]
    Burgin CJ, He K. 2018. Family Soricidae (shrews). In: Wilson DE, Mittermeier RA. Handbook of The Mammals of the World: Vol. 8: Insectivores, Sloths and Colugos. Barcelona: Lynx Edicions, 332−551.
    [8]
    Chen X, Ni G, He K, Ding ZL, Li GM, Adeola AC, et al. 2018. Capture hybridization of long-range DNA fragments for high-throughput sequencing. In: Huang T. Computational Systems Biology: Methods and Protocols. New York, NY: Springer, 29−44.
    [9]
    Choate JR. 1970. Systematics and zoogeography of the Middle American shrews of the genus Cryptotis. University of Kansas Museum of Natural History, 19(3): 195−317.
    [10]
    de Abreu-Jr EF, Pavan SE, Tsuchiya MTN, Wilson DE, Percequillo AR, Maldonado JE. 2020. Spatiotemporal diversification of tree squirrels: is the south American invasion and speciation really that recent and fast?. Frontiers in Ecology and Evolution, 8: 230. doi: 10.3389/fevo.2020.00230
    [11]
    Duchêne S, Archer FI, Vilstrup J, Caballero S, Morin PA. 2011. Mitogenome phylogenetics: the impact of using single regions and partitioning schemes on topology, substitution rate and divergence time estimation. PLoS One, 6(11): e27138.
    [12]
    Gan HM, Schultz MB, Austin CM. 2014. Integrated shotgun sequencing and bioinformatics pipeline allows ultra-fast mitogenome recovery and confirms substantial gene rearrangements in Australian freshwater crayfishes. BMC Evolutionary Biology, 14: 19. doi: 10.1186/1471-2148-14-19
    [13]
    Giarla TC, Esselstyn JA. 2015. The challenges of resolving a rapid, recent radiation: empirical and simulated phylogenomics of Philippine shrews. Systematic Biology, 64(5): 727−740.
    [14]
    Göker M, Voglmayr H, Blázquez GG, Oberwinkler F. 2009. Species delimitation in downy mildews: the case of Hyaloperonospora in the light of nuclear ribosomal ITS and LSU sequences. Mycological Research, 113(3): 308−325.
    [15]
    Guevara L. 2017. They can dig it: semifossorial habits of the Mexican small-eared shrew (Mammalia: Cryptotis mexicanus). Revista Mexicana de Biodiversidad, 88(4): 1003−1005.
    [16]
    He K, Chen X, Chen P, He SW, Cheng F, Jiang XL, et al. 2018. A new genus of Asiatic short-tailed shrew (Soricidae, Eulipotyphla) based on molecular and morphological comparisons. Zoological Research, 39(5): 321−334.
    [17]
    He K, Eastman TG, Czolacz H, Li SH, Shinohara A, Kawada SI, et al. 2021. Myoglobin primary structure reveals multiple convergent transitions to semi-aquatic life in the world’s smallest mammalian divers. eLife, 10: e66797. doi: 10.7554/eLife.66797
    [18]
    He K, Jiang XL. 2014. Sky islands of southwest China. I: an overview of phylogeographic patterns. Chinese Science Bulletin, 59(7): 585−597.
    [19]
    He K, Li YJ, Brandley MC, Lin LK, Wang YX, Zhang YP, et al. 2010. A multi-locus phylogeny of Nectogalini shrews and influences of the paleoclimate on speciation and evolution. Molecular Phylogenetics and Evolution, 56(2): 734−746.
    [20]
    He K, Woodman N, Boaglio S, Roberts M, Supekar S, Maldonado JE. 2015. Molecular phylogeny supports repeated adaptation to burrowing within small-eared shrews genus of Cryptotis (Eulipotyphla, Soricidae). PLoS One, 10(10): e0140280. doi: 10.1371/journal.pone.0140280
    [21]
    Heald WF. 1951. Sky-islands of Arizona. Natural History, 60: 56−63.
    [22]
    Huerta-Cepas J, Serra F, Bork P. 2016. ETE 3: reconstruction, analysis, and visualization of phylogenomic data. Molecular Biology and Evolution, 33(6): 1635−1638.
    [23]
    Hutterer R, Balete DS, Giarla TC, Heaney LR, Esselstyn JA. 2018. A new genus and species of shrew (Mammalia: Soricidae) from Palawan Island, Philippines. Journal of Mammalogy, 99(3): 518−536.
    [24]
    Kainer D, Lanfear R. 2015. The effects of partitioning on phylogenetic inference. Molecular Biology and Evolution, 32(6): 1611−1627.
    [25]
    Kearse M, Sturrock S, Meintjes P. 2012. The geneious 6.0. 3 read mapper. Auckland, New Zealand: Biomatters, Ltd.
    [26]
    Kishino H, Hasegawa M. 1989. Evaluation of the maximum likelihood estimate of the evolutionary tree topologies from DNA sequence data, and the branching order in Hominoidea. Journal of Molecular Evolution, 29(2): 170−179.
    [27]
    Lanfear R, Frandsen PB, Wright AM, Senfeld T, Calcott B. 2017. PartitionFinder 2: new methods for selecting partitioned models of evolution for molecular and morphological phylogenetic analyses. Molecular Biology and Evolution, 34(3): 772−773.
    [28]
    McCormack JE, Huang HT, Knowle LL. 2009. Sky islands. In: Gillespie RG, Clague DA. Encyclopedia of Islands. Berkeley, CA: University of California Press, 841−843.
    [29]
    Miller MA, Schwartz T, Pickett BE, He S, Klem EB, Scheuermann RH, et al. 2015. A RESTful API for access to phylogenetic tools via the CIPRES science gateway. Evolutionary Bioinformatics, 11: 43−48.
    [30]
    Pine RH, Woodman N, Timm RM. 2002. Rediscovery of Enders's small-eared shrew, Cryptotis endersi (Insectivora: Soricidae), with a redescription of the species. Mammalian Biology, 67(6): 372−377.
    [31]
    Ripma LA, Simpson MG, Hasenstab-Lehman K. 2014. Geneious! Simplified genome skimming methods for phylogenetic systematic studies: a case study in Oreocarya (Boraginaceae). Applications in Plant Sciences, 2(12): 1400062. doi: 10.3732/apps.1400062
    [32]
    Shimodaira H. 2002. An approximately unbiased test of phylogenetic tree selection. Systematic Biology, 51(3): 492−508.
    [33]
    Shimodaira H, Hasegawa M. 2001. CONSEL: for assessing the confidence of phylogenetic tree selection. Bioinformatics, 17(12): 1246−1247.
    [34]
    Stamatakis A. 2014. RAxML version 8: a tool for phylogenetic analysis and post-analysis of large phylogenies. Bioinformatics, 30(9): 1312−1313.
    [35]
    Swofford DL. 2003. PAUP*: phylogenetic analysis using parsimony (* and other methods). Version 4. Sinauer Associates, Sunderland.
    [36]
    Woodman N. 2019. American Recent Eulipotyphla: Nesophontids, Solenodons, Moles, and Shrews in the New World. Washington, DC: The Smithsonian Institution.
    [37]
    Woodman N, Gaffney SA. 2014. Can they dig it? Functional morphology and semifossoriality among small-eared shrews, genus Cryptotis (Mammalia, Soricidae). Journal of Morphology, 275(7): 745−759.
    [38]
    Woodman N, Timm RM. 1998. Geographic variation and evolutionary relationships among broad-clawed shrews of the Cryptotis goldmani-group (Mammalia: Insectivora: Soricidae). Fieldiana:Zoology (New Series), (91): 1−35.
    [39]
    Woodman N, Timm RM. 2017. A new species of small-eared shrew in the Cryptotis thomasi species group from Costa Rica (Mammalia: Eulipotyphla: Soricidae). Mammal Research, 62(1): 89−101.
    [40]
    Woodman N, Wilken AT. 2019. Comparative functional skeletal morphology among three genera of shrews: Implications for the evolution of locomotor behavior in the Soricinae (Eulipotyphla: Soricidae). Journal of Mammalogy, 100(6): 1750−1764.
    [41]
    Zeballos H, Pino K, Medina CE, Pari A, Chávez D, Tinoco N, et al. 2018. A new species of small-eared shrew of the genus Cryptotis (Mammalia, Eulipotyphla, Soricidae) from the northernmost Peruvian Andes. Zootaxa, 4377(1): 51−73.
    [42]
    Zimin AV, Smith DR, Sutton G, Yorke JA. 2008. Assembly reconciliation. Bioinformatics, 24(1): 42−45.
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