scholarly journals Autogenous and anautogenous Culex pipiens bioforms exhibit insulin-like peptide signaling pathway gene expression differences that are not dependent upon larval nutrition

2021 ◽  
Author(s):  
Alys M Cheatle Jarvela ◽  
Katherine Bell ◽  
Anna Noreuil ◽  
Megan Fritz

Culex pipiens form pipiens and Cx. pipiens form molestus differ in their ability to produce eggs without a bloodmeal. Autogenous mosquitoes, such as the molestus bioform of Cx. pipiens, depend on nutrition acquired as larvae instead of a bloodmeal to fuel the energy intensive process of vitellogenesis, which requires abundant production of yolk proteins. In anautogenous mosquito systems, ovary ecdysteroidogenic hormone (OEH) and insulin-like peptides (ILPs) transduce nutritional signals and trigger egg maturation in response to a bloodmeal. It is unclear to what extent the process is conserved in autogenous mosquitoes and how the bloodmeal trigger has been replaced by teneral reserves. Here, we measured the effects of a series of nutritional regimens on autogeny, time to pupation, and survival in Cx. pipiens form molestus and form pipiens. We find that abundant nutrients never result in autogenous form pipiens and extremely poor food availability rarely eliminates autogeny from form molestus. However, the number of autogenous eggs generated increases with nutrient availability. Similarly, using qPCR to quantify gene expression, we find several differences in the expression levels of ilps between bioforms that are reduced and delayed by poor nutrition, but not extinguished. Changes in OEH expression do not explain bioform-specific differences in autogeny. Surprisingly, the source of most of the gene expression differences correlated with autogeny is the abdomen, not the brain. Overall, our results suggest that autogeny is modulated by nutritional availability, but the trait is encoded by genetic differences between forms and these impact the expression of ILPs.  

Bone ◽  
2011 ◽  
Vol 48 ◽  
pp. S159
Author(s):  
T. Koromila ◽  
Z. Dailiana ◽  
S. Samara ◽  
C. Chassanidis ◽  
V. Aleporou - Marinou ◽  
...  

2017 ◽  
Vol 89 ◽  
pp. 8-14 ◽  
Author(s):  
Carolina da Silva Peixoto ◽  
Gustavo Morrone Parfitt ◽  
Gisele Eva Bruch ◽  
Marcos Freitas Cordeiro ◽  
Daniela Volcan Almeida ◽  
...  

2018 ◽  
Vol 470 ◽  
pp. 151-159 ◽  
Author(s):  
Eun Kyung Ko ◽  
Lynn P. Chorich ◽  
Megan E. Sullivan ◽  
Richard S. Cameron ◽  
Lawrence C. Layman

PLoS ONE ◽  
2010 ◽  
Vol 5 (7) ◽  
pp. e11749 ◽  
Author(s):  
Patric J. D. Delhanty ◽  
Yuxiang Sun ◽  
Jenny A. Visser ◽  
Anke van Kerkwijk ◽  
Martin Huisman ◽  
...  

2019 ◽  
Vol 17 (4) ◽  
pp. 106-110
Author(s):  
F. M. Kipkeeva ◽  
Т. А. Muzaffarova ◽  
M. P. Nikulin ◽  
P. V. Apanovich ◽  
S. N. Nered ◽  
...  

PeerJ ◽  
2017 ◽  
Vol 5 ◽  
pp. e2909 ◽  
Author(s):  
Tanya T. Cheung ◽  
Mitchell K. Weston ◽  
Megan J. Wilson

The development of the brain is sex-dimorphic, and as a result so are many neurological disorders. One approach for studying sex-dimorphic brain development is to measure gene expression in biological samples using RT-qPCR. However, the accuracy and consistency of this technique relies on the reference gene(s) selected. We analyzed the expression of ten reference genes in male and female samples over three stages of brain development, using popular algorithms NormFinder, GeNorm and Bestkeeper. The top ranked reference genes at each time point were further used to quantify gene expression of three sex-dimorphic genes (Wnt10b,XistandCYP7B1). When comparing gene expression between the sexes expression at specific time points the best reference gene combinations are:Sdha/Pgk1at E11.5,RpL38/SdhaE12.5, andActb/RpL37at E15.5. When studying expression across time, the ideal reference gene(s) differs with sex. For XY samples a combination ofActb/Sdha. In contrast, when studying gene expression across developmental stage with XX samples,Sdha/Gapdhwere the top reference genes. Our results identify the best combination of two reference genes when studying male and female brain development, and emphasize the importance of selecting the correct reference genes for comparisons between developmental stages.


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