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      Sex-specific effects of protein and carbohydrate intake on reproduction but not lifespan in Drosophila melanogaster

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          Abstract

          Modest dietary restriction extends lifespan (LS) in a diverse range of taxa and typically has a larger effect in females than males. Traditionally, this has been attributed to a stronger trade-off between LS and reproduction in females than in males that is mediated by the intake of calories. Recent studies, however, suggest that it is the intake of specific nutrients that extends LS and mediates this trade-off. Here, we used the geometric framework (GF) to examine the sex-specific effects of protein (P) and carbohydrate (C) intake on LS and reproduction in Drosophila melanogaster. We found that LS was maximized at a high intake of C and a low intake of P in both sexes, whereas nutrient intake had divergent effects on reproduction. Male offspring production rate and LS were maximized at the same intake of nutrients, whereas female egg production rate was maximized at a high intake of diets with a P:C ratio of 1:2. This resulted in larger differences in nutrient-dependent optima for LS and reproduction in females than in males, as well as an optimal intake of nutrients for lifetime reproduction that differed between the sexes. Under dietary choice, the sexes followed similar feeding trajectories regulated around a P:C ratio of 1:4. Consequently, neither sex reached their nutritional optimum for lifetime reproduction, suggesting intralocus sexual conflict over nutrient optimization. Our study shows clear sex differences in the nutritional requirements of reproduction in D. melanogaster and joins the growing list of studies challenging the role of caloric restriction in extending LS.

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          The Measurement of Selection on Correlated Characters

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            Acquisition and Allocation of Resources: Their Influence on Variation in Life History Tactics

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              Intralocus sexual conflict.

              Intralocus sexual conflict occurs when selection on a shared trait in one sex displaces the other sex from its phenotypic optimum. It arises because many shared traits have a common genetic basis but undergo contrasting selection in the sexes. A recent surge of interest in this evolutionary tug of war has yielded evidence of such conflicts in laboratory and natural populations. Here we highlight outstanding questions about the causes and consequences of intralocus sexual conflict at the genomic level, and its long-term implications for sexual coevolution. Whereas recent thinking has focussed on the role of intralocus sexual conflict as a brake on sexual coevolution, we urge a broader appraisal that also takes account of its potential to drive adaptive evolution and speciation.
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                Author and article information

                Journal
                Aging Cell
                Aging Cell
                acel
                Aging Cell
                John Wiley & Sons, Ltd (Chichester, UK )
                1474-9718
                1474-9726
                August 2015
                23 March 2015
                : 14
                : 4
                : 605-615
                Affiliations
                [1 ]Centre for Ecology and Conservation, College of Life and Environmental Sciences, University of Exeter, Cornwall Campus Penryn, TR10 9EZ, UK
                [2 ]Department of Biology and Biochemistry, University of Bath Bath, BA2 7AY, UK
                Author notes
                Correspondence, John Hunt, Centre for Ecology and Conservation, College of Life and Environmental Sciences, University of Exeter, Cornwall Campus, Penryn TR10 9EZ, UK. Tel.: +44 (0) 1326 371892; fax: +44 (0) 1326 253638; e-mail: J.Hunt@ 123456exeter.ac.uk
                Article
                10.1111/acel.12333
                4531074
                25808180
                f126279f-06c1-4254-b14a-ea141f07177d
                © 2015 The Authors. Aging Cell published by the Anatomical Society and John Wiley & Sons Ltd.

                This is an open access article under the terms of the Creative Commons Attribution License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.

                History
                : 28 January 2015
                Categories
                Original Articles

                Cell biology
                caloric restriction,fitness,geometric framework,lifespan,nutrient regulation,reproduction
                Cell biology
                caloric restriction, fitness, geometric framework, lifespan, nutrient regulation, reproduction

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