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Role of the venus kinase receptor in the female reproductive physiology of the desert locust, Schistocerca gregaria

Venus kinase receptors (VKR) are a subfamily of invertebrate receptor tyrosine kinases, which have only recently been discovered. They contain an intracellular tyrosine kinase domain and an extracellular Venus FlyTrap domain. VKRs have been functionally and pharmacologically characterized in only tw...

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Autores principales: Lenaerts, Cynthia, Palmans, Jolien, Marchal, Elisabeth, Verdonck, Rik, Vanden Broeck, Jozef
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5601475/
https://www.ncbi.nlm.nih.gov/pubmed/28916758
http://dx.doi.org/10.1038/s41598-017-11434-3
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author Lenaerts, Cynthia
Palmans, Jolien
Marchal, Elisabeth
Verdonck, Rik
Vanden Broeck, Jozef
author_facet Lenaerts, Cynthia
Palmans, Jolien
Marchal, Elisabeth
Verdonck, Rik
Vanden Broeck, Jozef
author_sort Lenaerts, Cynthia
collection PubMed
description Venus kinase receptors (VKR) are a subfamily of invertebrate receptor tyrosine kinases, which have only recently been discovered. They contain an intracellular tyrosine kinase domain and an extracellular Venus FlyTrap domain. VKRs have been functionally and pharmacologically characterized in only two invertebrate species, namely the human parasite Schistosoma mansoni and the mosquito Aedes aegypti, where they play a crucial role in oogenesis. Here, we report the characterization of a VKR in the desert locust, Schistocerca gregaria. We performed an in-depth profiling study of the SgVKR transcript levels in different tissues throughout the female adult stage. Using the RNA interference technique, the possible role of SgVKR was investigated. SgVKR knockdown had significant effects on ovarian ecdysteroid levels and on the size of oocytes during the vitellogenic stage. SgVKR is probably involved in the complex cross-talk between several important pathways regulating female reproductive physiology. Contrary to A. aegypti and S. mansoni, we cannot conclude that this receptor is essential for reproduction, since silencing SgVKR did not affect fecundity or fertility. Considering the evolutionary distance between A. aegypti and S. gregaria, as well as the differences in regulation of their female reproductive physiology, this article constitutes a valuable asset in better understanding VKRs.
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spelling pubmed-56014752017-09-20 Role of the venus kinase receptor in the female reproductive physiology of the desert locust, Schistocerca gregaria Lenaerts, Cynthia Palmans, Jolien Marchal, Elisabeth Verdonck, Rik Vanden Broeck, Jozef Sci Rep Article Venus kinase receptors (VKR) are a subfamily of invertebrate receptor tyrosine kinases, which have only recently been discovered. They contain an intracellular tyrosine kinase domain and an extracellular Venus FlyTrap domain. VKRs have been functionally and pharmacologically characterized in only two invertebrate species, namely the human parasite Schistosoma mansoni and the mosquito Aedes aegypti, where they play a crucial role in oogenesis. Here, we report the characterization of a VKR in the desert locust, Schistocerca gregaria. We performed an in-depth profiling study of the SgVKR transcript levels in different tissues throughout the female adult stage. Using the RNA interference technique, the possible role of SgVKR was investigated. SgVKR knockdown had significant effects on ovarian ecdysteroid levels and on the size of oocytes during the vitellogenic stage. SgVKR is probably involved in the complex cross-talk between several important pathways regulating female reproductive physiology. Contrary to A. aegypti and S. mansoni, we cannot conclude that this receptor is essential for reproduction, since silencing SgVKR did not affect fecundity or fertility. Considering the evolutionary distance between A. aegypti and S. gregaria, as well as the differences in regulation of their female reproductive physiology, this article constitutes a valuable asset in better understanding VKRs. Nature Publishing Group UK 2017-09-15 /pmc/articles/PMC5601475/ /pubmed/28916758 http://dx.doi.org/10.1038/s41598-017-11434-3 Text en © The Author(s) 2017 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Lenaerts, Cynthia
Palmans, Jolien
Marchal, Elisabeth
Verdonck, Rik
Vanden Broeck, Jozef
Role of the venus kinase receptor in the female reproductive physiology of the desert locust, Schistocerca gregaria
title Role of the venus kinase receptor in the female reproductive physiology of the desert locust, Schistocerca gregaria
title_full Role of the venus kinase receptor in the female reproductive physiology of the desert locust, Schistocerca gregaria
title_fullStr Role of the venus kinase receptor in the female reproductive physiology of the desert locust, Schistocerca gregaria
title_full_unstemmed Role of the venus kinase receptor in the female reproductive physiology of the desert locust, Schistocerca gregaria
title_short Role of the venus kinase receptor in the female reproductive physiology of the desert locust, Schistocerca gregaria
title_sort role of the venus kinase receptor in the female reproductive physiology of the desert locust, schistocerca gregaria
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5601475/
https://www.ncbi.nlm.nih.gov/pubmed/28916758
http://dx.doi.org/10.1038/s41598-017-11434-3
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