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Novel microsatellite markers suggest the mechanism of parthenogenesis in Extatosoma tiaratum is automixis with terminal fusion
Parthenogenetic reproduction is taxonomically widespread and occurs through various cytological mechanisms, which have different impact on the genetic variation of the offspring. Extatosoma tiaratum is a facultatively parthenogenetic Australian insect (Phasmatodea), in which females oviposit continu...
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Published in: | Insect science 2018-02, Vol.25 (1), p.24-32 |
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creator | Alavi, Yasaman Rooyen, Anthony Elgar, Mark Adrian Jones, Therésa Melanie Weeks, Andrew Raymond |
description | Parthenogenetic reproduction is taxonomically widespread and occurs through various cytological mechanisms, which have different impact on the genetic variation of the offspring. Extatosoma tiaratum is a facultatively parthenogenetic Australian insect (Phasmatodea), in which females oviposit continuously throughout their adult lifespan irrespective of mating. Fertilized eggs produce sons and daughters through sexual reproduction and unfertilized eggs produce female offspring via parthenogenesis. Here, we developed novel microsatellite markers for E. tiaratum and characterized them by genotyping individuals from a natural population. We then used the microsatellite markers to infer the cytological mechanism of parthenogenesis in this species. We found evidence suggesting parthenogenesis in E. tiaratum occurs through automixis with terminal fusion, resulting in substantial loss of microsatellite heterozygosity in the offspring. Loss of microsatellite heterozygosity may be associated with loss of heterozygosity in fitness related loci. The mechanism of parthenogenetic reproduction can therefore affect fitness outcomes and needs to be considered when comparing costs and benefits of sex versus parthenogenesis. |
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Extatosoma tiaratum is a facultatively parthenogenetic Australian insect (Phasmatodea), in which females oviposit continuously throughout their adult lifespan irrespective of mating. Fertilized eggs produce sons and daughters through sexual reproduction and unfertilized eggs produce female offspring via parthenogenesis. Here, we developed novel microsatellite markers for E. tiaratum and characterized them by genotyping individuals from a natural population. We then used the microsatellite markers to infer the cytological mechanism of parthenogenesis in this species. We found evidence suggesting parthenogenesis in E. tiaratum occurs through automixis with terminal fusion, resulting in substantial loss of microsatellite heterozygosity in the offspring. Loss of microsatellite heterozygosity may be associated with loss of heterozygosity in fitness related loci. 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Extatosoma tiaratum is a facultatively parthenogenetic Australian insect (Phasmatodea), in which females oviposit continuously throughout their adult lifespan irrespective of mating. Fertilized eggs produce sons and daughters through sexual reproduction and unfertilized eggs produce female offspring via parthenogenesis. Here, we developed novel microsatellite markers for E. tiaratum and characterized them by genotyping individuals from a natural population. We then used the microsatellite markers to infer the cytological mechanism of parthenogenesis in this species. We found evidence suggesting parthenogenesis in E. tiaratum occurs through automixis with terminal fusion, resulting in substantial loss of microsatellite heterozygosity in the offspring. Loss of microsatellite heterozygosity may be associated with loss of heterozygosity in fitness related loci. The mechanism of parthenogenetic reproduction can therefore affect fitness outcomes and needs to be considered when comparing costs and benefits of sex versus parthenogenesis.</description><subject>Animals</subject><subject>apomixis</subject><subject>automixis</subject><subject>Cost benefit analysis</subject><subject>Eggs</subject><subject>Extatosoma tiaratum</subject><subject>Female</subject><subject>Females</subject><subject>Fitness</subject><subject>Genetic diversity</subject><subject>Genetic markers</subject><subject>Genotyping</subject><subject>Heterozygosity</subject><subject>Inheritance Patterns</subject><subject>Insecta - physiology</subject><subject>Insects</subject><subject>Life span</subject><subject>Loss of heterozygosity</subject><subject>Male</subject><subject>Markers</subject><subject>Mating</subject><subject>microsatellite markers</subject><subject>Microsatellite Repeats</subject><subject>Microsatellites</subject><subject>Offspring</subject><subject>Parthenogenesis</subject><subject>Reproduction</subject><subject>Reproduction (biology)</subject><subject>Reproductive fitness</subject><subject>Sexual reproduction</subject><issn>1672-9609</issn><issn>1744-7917</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2018</creationdate><recordtype>article</recordtype><recordid>eNqFkb1PHDEQxa0oKHwkdbrIUhqaBX-s1-syQiSchKCA1Nbsrn1nsl5fbG-Ahr89Pu6goMGNR88_P83MQ-grJSe0nFMq67qSisoTyrjkH9DBq_Kx1I1klWqI2keHKd0RwhVT7BPaZ5LXQrTyAD1dhX9mxN71MSTIZhxdNthD_GNiwmleLk3KOK-KZvoVTC55HCxeQyzaFJZmMskl7CZ8_pAhhxQ84OwgQp49Li8w5-DdQ6nuXV7hbKJ3E4zYzsmF6TPaszAm82V3H6HfP89vzy6qy-tfi7Mfl1Vfl8Eq05IGBquE7CkdmLWKK1IrImvgfSfI0AtrGRtaIjrTAW2bnnAKgnddPdgO-BE63vquY_g7l5G0d6kv08Jkwpw0bVkjKW8JLej3N-hdmGNpuVCqVVIJSlShTrfUZm8pGqvX0ZW1PWpK9CYavQlCb4LQz9GUH992vnPnzfDKv2RRALEF7t1oHt_z04urm63xf_xOm3M</recordid><startdate>201802</startdate><enddate>201802</enddate><creator>Alavi, Yasaman</creator><creator>Rooyen, Anthony</creator><creator>Elgar, Mark Adrian</creator><creator>Jones, Therésa Melanie</creator><creator>Weeks, Andrew Raymond</creator><general>Wiley Subscription Services, Inc</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QG</scope><scope>7QR</scope><scope>7SN</scope><scope>7SS</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>P64</scope><scope>7X8</scope></search><sort><creationdate>201802</creationdate><title>Novel microsatellite markers suggest the mechanism of parthenogenesis in Extatosoma tiaratum is automixis with terminal fusion</title><author>Alavi, Yasaman ; 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subjects | Animals apomixis automixis Cost benefit analysis Eggs Extatosoma tiaratum Female Females Fitness Genetic diversity Genetic markers Genotyping Heterozygosity Inheritance Patterns Insecta - physiology Insects Life span Loss of heterozygosity Male Markers Mating microsatellite markers Microsatellite Repeats Microsatellites Offspring Parthenogenesis Reproduction Reproduction (biology) Reproductive fitness Sexual reproduction |
title | Novel microsatellite markers suggest the mechanism of parthenogenesis in Extatosoma tiaratum is automixis with terminal fusion |
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