TY - JOUR
T1 - Positional RNA-Seq identifies candidate genes for phenotypic engineering of sexual traits
AU - Arbore, Roberto
AU - Sekii, Kiyono
AU - Beisel, Christian
AU - Ladurner, Peter
AU - Berezikov, Eugene
AU - Schärer, Lukas
N1 - Funding Information:
The authors would like to thank all members of the Schärer research group, and in particular Dita Vizoso, for help in the laboratory, and Jürgen Hottinger, Viktor Mislin, Urs Stiefel and Lukas Zimmermann for technical support. We also thank Dieter Ebert and Walter Salzburger for helpful discussions during the conception of this study, Piero Cervella for technical advice, and Steve Ramm and two anonymous reviewers for valuable comments on earlier versions of the manuscript. P.L. is supported by FWF 25404. This work was funded by grants of the Swiss National Science Foundation to LS (SNF grants 3100A0-127503 and 31003A-143732).
Publisher Copyright:
© 2015 Arbore et al.
PY - 2015/7/3
Y1 - 2015/7/3
N2 - Introduction: RNA interference (RNAi) of trait-specific genes permits the manipulation of specific phenotypic traits ("phenotypic engineering") and thus represents a powerful tool to test trait function in evolutionary studies. The identification of suitable candidate genes, however, often relies on existing functional gene annotation, which is usually limited in emerging model organisms, especially when they are only distantly related to traditional genetic model organisms. A case in point is the free-living flatworm Macrostomum lignano (Lophotrochozoa: Platyhelminthes: Rhabditophora), an increasingly powerful model organism for evolutionary studies of sex in simultaneous hermaphrodites. To overcome the limitation of sparse functional annotation, we have performed a positional RNA-Seq analysis on different body fragments in order to identify organ-specific candidate transcripts. We then performed gene expression (in situ hybridization) and gene function (RNAi) analyses on 23 candidate transcripts, both to evaluate the predictive potential of this approach and to obtain preliminary functional characterizations of these candidate genes. Results: We identified over 4000 transcripts that could be expected to show specific expression in different reproductive organs (including testis, ovary and the male and female genital systems). The predictive potential of the method could then be verified by confirming organ-specific expression for several candidate transcripts, some of which yielded interesting trait-specific knock-down phenotypes that can now be followed up in future phenotypic engineering studies. Conclusions: Our positional RNA-Seq analysis represents a highly useful resource for the identification of candidate transcripts for functional and phenotypic engineering studies in M. lignano, and it has already been used successfully in several studies. Moreover, this approach can overcome some inherent limitations of homology-based candidate selection and thus should be applicable to a broad range of emerging model organisms.
AB - Introduction: RNA interference (RNAi) of trait-specific genes permits the manipulation of specific phenotypic traits ("phenotypic engineering") and thus represents a powerful tool to test trait function in evolutionary studies. The identification of suitable candidate genes, however, often relies on existing functional gene annotation, which is usually limited in emerging model organisms, especially when they are only distantly related to traditional genetic model organisms. A case in point is the free-living flatworm Macrostomum lignano (Lophotrochozoa: Platyhelminthes: Rhabditophora), an increasingly powerful model organism for evolutionary studies of sex in simultaneous hermaphrodites. To overcome the limitation of sparse functional annotation, we have performed a positional RNA-Seq analysis on different body fragments in order to identify organ-specific candidate transcripts. We then performed gene expression (in situ hybridization) and gene function (RNAi) analyses on 23 candidate transcripts, both to evaluate the predictive potential of this approach and to obtain preliminary functional characterizations of these candidate genes. Results: We identified over 4000 transcripts that could be expected to show specific expression in different reproductive organs (including testis, ovary and the male and female genital systems). The predictive potential of the method could then be verified by confirming organ-specific expression for several candidate transcripts, some of which yielded interesting trait-specific knock-down phenotypes that can now be followed up in future phenotypic engineering studies. Conclusions: Our positional RNA-Seq analysis represents a highly useful resource for the identification of candidate transcripts for functional and phenotypic engineering studies in M. lignano, and it has already been used successfully in several studies. Moreover, this approach can overcome some inherent limitations of homology-based candidate selection and thus should be applicable to a broad range of emerging model organisms.
KW - Macrostomum lignano
KW - Phenotypic engineering
KW - RNA interference
KW - RNA-Seq
KW - simultaneous hermaphrodite
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U2 - 10.1186/s12983-015-0106-0
DO - 10.1186/s12983-015-0106-0
M3 - Article
AN - SCOPUS:84934754214
SN - 1742-9994
VL - 12
JO - Frontiers in Zoology
JF - Frontiers in Zoology
IS - 1
M1 - 14
ER -