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The Genomic Load of Deleterious Mutations: Relevance to Death in Infancy and Childhood

The human diploid genome has approximately 40,000 functioning conserved genes distributed within 6 billion base pairs of DNA. Most individuals carry a few heterozygous deleterious mutations and this leads to an increased risk of recessive disease in the offspring of cousin unions. Rare recessive dis...

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Autor principal: Morris, James Alfred
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4360568/
https://www.ncbi.nlm.nih.gov/pubmed/25852684
http://dx.doi.org/10.3389/fimmu.2015.00105
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author Morris, James Alfred
author_facet Morris, James Alfred
author_sort Morris, James Alfred
collection PubMed
description The human diploid genome has approximately 40,000 functioning conserved genes distributed within 6 billion base pairs of DNA. Most individuals carry a few heterozygous deleterious mutations and this leads to an increased risk of recessive disease in the offspring of cousin unions. Rare recessive disease is more common in the children of cousin marriages than in the general population, even though <1% of marriages in the Western World are between first cousins. But more than 90% of the children of cousin marriages do not have recessive disease and are as healthy as the rest of the population. A mathematical model based on these observations generates simultaneous equations linking the mean number of deleterious mutations in the genome of adults (M), the mean number of new deleterious mutations arising in gametogenesis and passed to the next generation (N) and the number of genes in the human diploid genome (L). The best estimates are that M is <7 and N is approximately 1. The nature of meiosis indicates that deleterious mutations in zygotes will have a Poisson distribution with a mean of M + N. There must be strong selective pressure against zygotes at the upper end of the Poisson distribution otherwise the value of M would rise with each generation. It is suggested that this selection is based on synergistic interaction of heterozygous deleterious mutations acting in large complex highly redundant and robust genetic networks. To maintain the value of M in single figures over many thousands of generations means that the zygote loss must be of the order of 30%. Most of this loss will occur soon after conception but some will occur later; during fetal development, in infancy and even in childhood. Selection means genetic death and this is caused by disease to which the deleterious mutations predispose. In view of this genome sequencing should be undertaken in all infant deaths in which the cause of death is not ascertained by standard techniques.
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spelling pubmed-43605682015-04-07 The Genomic Load of Deleterious Mutations: Relevance to Death in Infancy and Childhood Morris, James Alfred Front Immunol Immunology The human diploid genome has approximately 40,000 functioning conserved genes distributed within 6 billion base pairs of DNA. Most individuals carry a few heterozygous deleterious mutations and this leads to an increased risk of recessive disease in the offspring of cousin unions. Rare recessive disease is more common in the children of cousin marriages than in the general population, even though <1% of marriages in the Western World are between first cousins. But more than 90% of the children of cousin marriages do not have recessive disease and are as healthy as the rest of the population. A mathematical model based on these observations generates simultaneous equations linking the mean number of deleterious mutations in the genome of adults (M), the mean number of new deleterious mutations arising in gametogenesis and passed to the next generation (N) and the number of genes in the human diploid genome (L). The best estimates are that M is <7 and N is approximately 1. The nature of meiosis indicates that deleterious mutations in zygotes will have a Poisson distribution with a mean of M + N. There must be strong selective pressure against zygotes at the upper end of the Poisson distribution otherwise the value of M would rise with each generation. It is suggested that this selection is based on synergistic interaction of heterozygous deleterious mutations acting in large complex highly redundant and robust genetic networks. To maintain the value of M in single figures over many thousands of generations means that the zygote loss must be of the order of 30%. Most of this loss will occur soon after conception but some will occur later; during fetal development, in infancy and even in childhood. Selection means genetic death and this is caused by disease to which the deleterious mutations predispose. In view of this genome sequencing should be undertaken in all infant deaths in which the cause of death is not ascertained by standard techniques. Frontiers Media S.A. 2015-03-16 /pmc/articles/PMC4360568/ /pubmed/25852684 http://dx.doi.org/10.3389/fimmu.2015.00105 Text en Copyright © 2015 Morris. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Immunology
Morris, James Alfred
The Genomic Load of Deleterious Mutations: Relevance to Death in Infancy and Childhood
title The Genomic Load of Deleterious Mutations: Relevance to Death in Infancy and Childhood
title_full The Genomic Load of Deleterious Mutations: Relevance to Death in Infancy and Childhood
title_fullStr The Genomic Load of Deleterious Mutations: Relevance to Death in Infancy and Childhood
title_full_unstemmed The Genomic Load of Deleterious Mutations: Relevance to Death in Infancy and Childhood
title_short The Genomic Load of Deleterious Mutations: Relevance to Death in Infancy and Childhood
title_sort genomic load of deleterious mutations: relevance to death in infancy and childhood
topic Immunology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4360568/
https://www.ncbi.nlm.nih.gov/pubmed/25852684
http://dx.doi.org/10.3389/fimmu.2015.00105
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