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A genetic tool to manipulate litter size

INTRODUCTION: Experimental litter size manipulations are often not problem free. Typically conducted shortly after birth or oviposition, they do not account for the energy already invested into the production of the offspring. Such effects make it difficult to interpret the results from experimental...

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Detalles Bibliográficos
Autores principales: Ferrari, Manuela, Lindholm, Anna K, König, Barbara
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3941797/
https://www.ncbi.nlm.nih.gov/pubmed/24564853
http://dx.doi.org/10.1186/1742-9994-11-18
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author Ferrari, Manuela
Lindholm, Anna K
König, Barbara
author_facet Ferrari, Manuela
Lindholm, Anna K
König, Barbara
author_sort Ferrari, Manuela
collection PubMed
description INTRODUCTION: Experimental litter size manipulations are often not problem free. Typically conducted shortly after birth or oviposition, they do not account for the energy already invested into the production of the offspring. Such effects make it difficult to interpret the results from experimental litter size manipulations and therefore to study optimality of litter or clutch size, a long debated topic in evolutionary biology. RESULTS: We propose the use of a mating design based on a selfish genetic element, the t haplotype, to reduce litter size in an eutherian mammal, the house mouse. Most t haplotypes are recessive lethal and therefore lead to the death of all homozygous embryos. Litter sizes can be reduced by up to 50% by pairing a +/t female with a +/t male instead of a +/+ male. CONCLUSIONS: This method allows litter size manipulation before birth without the use of invasive techniques, therefore providing an excellent tool for studying optimal litter size and ultimately helping to understand life history strategies.
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spelling pubmed-39417972014-03-05 A genetic tool to manipulate litter size Ferrari, Manuela Lindholm, Anna K König, Barbara Front Zool Methodology INTRODUCTION: Experimental litter size manipulations are often not problem free. Typically conducted shortly after birth or oviposition, they do not account for the energy already invested into the production of the offspring. Such effects make it difficult to interpret the results from experimental litter size manipulations and therefore to study optimality of litter or clutch size, a long debated topic in evolutionary biology. RESULTS: We propose the use of a mating design based on a selfish genetic element, the t haplotype, to reduce litter size in an eutherian mammal, the house mouse. Most t haplotypes are recessive lethal and therefore lead to the death of all homozygous embryos. Litter sizes can be reduced by up to 50% by pairing a +/t female with a +/t male instead of a +/+ male. CONCLUSIONS: This method allows litter size manipulation before birth without the use of invasive techniques, therefore providing an excellent tool for studying optimal litter size and ultimately helping to understand life history strategies. BioMed Central 2014-02-24 /pmc/articles/PMC3941797/ /pubmed/24564853 http://dx.doi.org/10.1186/1742-9994-11-18 Text en Copyright © 2014 Ferrari et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited.
spellingShingle Methodology
Ferrari, Manuela
Lindholm, Anna K
König, Barbara
A genetic tool to manipulate litter size
title A genetic tool to manipulate litter size
title_full A genetic tool to manipulate litter size
title_fullStr A genetic tool to manipulate litter size
title_full_unstemmed A genetic tool to manipulate litter size
title_short A genetic tool to manipulate litter size
title_sort genetic tool to manipulate litter size
topic Methodology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3941797/
https://www.ncbi.nlm.nih.gov/pubmed/24564853
http://dx.doi.org/10.1186/1742-9994-11-18
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