0
views
0
recommends
+1 Recommend
0 collections
    0
    shares
      • Record: found
      • Abstract: found
      • Article: found
      Is Open Access

      More evidence for widespread antagonistic pleiotropy in polymorphic disease alleles

      review-article

      Read this article at

      Bookmark
          There is no author summary for this article yet. Authors can add summaries to their articles on ScienceOpen to make them more accessible to a non-specialist audience.

          Abstract

          Introduction

          Many loci segregate alleles classified as “genetic diseases” due to their deleterious effects on health. However, some disease alleles have been reported to show beneficial effects under certain conditions or in certain populations. The beneficial effects of these antagonistically pleiotropic alleles may explain their continued prevalence, but the degree to which antagonistic pleiotropy is common or rare is unresolved. We surveyed the medical literature to identify examples of antagonistic pleiotropy to help determine whether antagonistic pleiotropy appears to be rare or common.

          Results

          We identified ten examples of loci with polymorphisms for which the presence of antagonistic pleiotropy is well supported by detailed genetic or epidemiological information in humans. One additional locus was identified for which the supporting evidence comes from animal studies. These examples complement over 20 others reported in other reviews.

          Discussion

          The existence of more than 30 identified antagonistically pleiotropic human disease alleles suggests that this phenomenon may be widespread. This poses important implications for both our understanding of human evolutionary genetics and our approaches to clinical treatment and disease prevention, especially therapies based on genetic modification.

          Related collections

          Most cited references194

          • Record: found
          • Abstract: found
          • Article: not found

          Statistical method for testing the neutral mutation hypothesis by DNA polymorphism.

          F Tajima (1989)
          The relationship between the two estimates of genetic variation at the DNA level, namely the number of segregating sites and the average number of nucleotide differences estimated from pairwise comparison, is investigated. It is found that the correlation between these two estimates is large when the sample size is small, and decreases slowly as the sample size increases. Using the relationship obtained, a statistical method for testing the neutral mutation hypothesis is developed. This method needs only the data of DNA polymorphism, namely the genetic variation within population at the DNA level. A simple method of computer simulation, that was used in order to obtain the distribution of a new statistic developed, is also presented. Applying this statistical method to the five regions of DNA sequences in Drosophila melanogaster, it is found that large insertion/deletion (greater than 100 bp) is deleterious. It is suggested that the natural selection against large insertion/deletion is so weak that a large amount of variation is maintained in a population.
            Bookmark
            • Record: found
            • Abstract: found
            • Article: not found

            Development and applications of CRISPR-Cas9 for genome engineering.

            Recent advances in genome engineering technologies based on the CRISPR-associated RNA-guided endonuclease Cas9 are enabling the systematic interrogation of mammalian genome function. Analogous to the search function in modern word processors, Cas9 can be guided to specific locations within complex genomes by a short RNA search string. Using this system, DNA sequences within the endogenous genome and their functional outputs are now easily edited or modulated in virtually any organism of choice. Cas9-mediated genetic perturbation is simple and scalable, empowering researchers to elucidate the functional organization of the genome at the systems level and establish causal linkages between genetic variations and biological phenotypes. In this Review, we describe the development and applications of Cas9 for a variety of research or translational applications while highlighting challenges as well as future directions. Derived from a remarkable microbial defense system, Cas9 is driving innovative applications from basic biology to biotechnology and medicine. Copyright © 2014 Elsevier Inc. All rights reserved.
              Bookmark
              • Record: found
              • Abstract: not found
              • Article: not found

              Pleiotropy, Natural Selection, and the Evolution of Senescence

                Bookmark

                Author and article information

                Contributors
                Role: Role: Role: Role: Role: Role:
                Role: Role: Role:
                URI : https://loop.frontiersin.org/people/2695043/overviewRole: Role: Role: Role: Role: Role:
                Journal
                Front Genet
                Front Genet
                Front. Genet.
                Frontiers in Genetics
                Frontiers Media S.A.
                1664-8021
                17 June 2024
                2024
                : 15
                : 1404516
                Affiliations
                California State University Long Beach , Department of Biological Sciences , Long Beach, CA, United States
                Author notes

                Edited by: Susana Seixas, Universidade do Porto, Portugal

                Reviewed by: Juan Antonio Rodriguez, University of Copenhagen, Denmark

                Igor B. Rogozin, University of Ostrava, Czechia

                *Correspondence: Ashley J. R. Carter, ashley.carter@ 123456csulb.edu
                Article
                1404516
                10.3389/fgene.2024.1404516
                11215129
                38952711
                d54e0beb-b063-43c4-87d1-17989efdde1e
                Copyright © 2024 Lockwood, Vo, Bellafard and Carter.

                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) and the copyright owner(s) 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.

                History
                : 21 March 2024
                : 29 May 2024
                Funding
                The author(s) declare that financial support was received for the research, authorship, and/or publication of this article. The project was supported in part by the National Institute of General Medical Sciences of the National Institutes of Health under Award Numbers 5UL1GM118979-03, 5TL4GM118980-03, 5RL5GM118978-03, and 5R01MH105398-TWB via financial support for the studies of HB.
                Categories
                Genetics
                Review
                Custom metadata
                Evolutionary and Population Genetics

                Genetics
                antagonistic pleiotropy,genetic disease,balancing selection,heterozygote advantage,overdominance

                Comments

                Comment on this article