Abstract

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.

Highlights

  • Infant mortality rates have fallen progressively in UK in the last 50 years, from 18 infant deaths per 1000 live births in 1970 to 4/1000 in 2012 [1]

  • GENOME WIDE ASSOCIATION STUDIES IN INFANT DEATH In genome wide association studies (GWAS), up to 500,000 common polymorphisms are assessed in a large cohort of individuals with a specific disease and this is compared with a large cohort of controls from the general population [18,19,20,21,22,23,24,25,26,27,28,29,30,31,32]

  • Our attention should focus on bacteria of the normal microbial flora and how they could interact with a genome impaired by deleterious mutations [42, 43]

Read more

Summary

James Alfred Morris*

Reviewed by: Caroline Blackwell, University of Newcastle, Australia Rodney J. The human diploid genome has approximately 40,000 functioning conserved genes distributed within 6 billion base pairs of DNA. 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

INTRODUCTION
Findings
DISCUSSION
Full Text
Paper version not known

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.