Reproductive Isolation of Hybrid Populations Driven by Genetic Incompatibilities
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A Genome-Wide Survey of Hybrid Incompatibility Factors by the Introgression of Marked Segments of Drosophila Mauritiana Chromosomes Into Drosophila Simulans
Copyright Q 1996 by the Genetics Society of America A Genome-Wide Survey of Hybrid Incompatibility Factors by the Introgression of Marked Segments of Drosophila mauritiana Chromosomes into Drosophila simulans John R. True,* Bruce S. Weirt and Cathy C. Laurie” *Department of Zoology, Duke University, Durham, North Carolina 27708 and tDepartrnent of Statistics, North Carolina State University, Raleigh, North Carolina 27695 Manuscript received August 31, 1995 Accepted for publication November 29, 1995 ABSTRACT In hybrids between Drosophila simulans and D. mauritiana, males are sterile and females are fertile, in compliance with HALDANE’S rule. The geneticbasis of this phenomenon was investigated by introgression of segments of the mauritiana genome into a simulans background. A total of 87 positions throughout the mauritiana genome were marked with P‘lement insertions and replicate introgressionswere made by repeated backcrossing to simulans for 15 generations. The fraction of hemizgyous X chromosomal introgressions that aremale sterile is -50% greater than the fractionof homozygous autosomal segments. This result suggests that male sterility factors have evolvedat a higher rate on the X, but chromosomal differences in segment length cannot be ruled out. The fractionof homozygous autosomal introgressions that are male sterile is several times greater than the fraction that are either female sterile or inviable. This observation strongly indicates that male sterility factors have evolved more rapidly than either female sterility or inviability factors. These results, combined with previous work on these and other species, suggest that HALDANE’S rule has at least two causes: recessivity of incompatibility factors and differential accumulation of sterility factors affecting males and females. -
2020 Program Book
PROGRAM BOOK Note that TAGC was cancelled and held online with a different schedule and program. This document serves as a record of the original program designed for the in-person meeting. April 22–26, 2020 Gaylord National Resort & Convention Center Metro Washington, DC TABLE OF CONTENTS About the GSA ........................................................................................................................................................ 3 Conference Organizers ...........................................................................................................................................4 General Information ...............................................................................................................................................7 Mobile App ....................................................................................................................................................7 Registration, Badges, and Pre-ordered T-shirts .............................................................................................7 Oral Presenters: Speaker Ready Room - Camellia 4.......................................................................................7 Poster Sessions and Exhibits - Prince George’s Exhibition Hall ......................................................................7 GSA Central - Booth 520 ................................................................................................................................8 Internet Access ..............................................................................................................................................8 -
Title: the Genomic Consequences of Hybridization Authors
Title: The genomic consequences of hybridization Authors: Benjamin M Moran1,2*+, Cheyenne Payne1,2*+, Quinn Langdon1, Daniel L Powell1,2, Yaniv Brandvain3, Molly Schumer1,2,4+ Affiliations: 1Department of Biology, Stanford University, Stanford, CA, USA 2Centro de Investigaciones Científicas de las Huastecas “Aguazarca”, A.C., Calnali, Hidalgo, Mexico 3Department of Ecology, Evolution & Behavior and Plant and Microbial Biology, University of Minnesota, St. Paul, MN, USA 4Hanna H. Gray Fellow, Howard Hughes Medical Institute, Stanford, CA, USA *Contributed equally to this work +Correspondence: [email protected], [email protected], [email protected] Abstract In the past decade, advances in genome sequencing have allowed researchers to uncover the history of hybridization in diverse groups of species, including our own. Although the field has made impressive progress in documenting the extent of natural hybridization, both historical and recent, there are still many unanswered questions about its genetic and evolutionary consequences. Recent work has suggested that the outcomes of hybridization in the genome may be in part predictable, but many open questions about the nature of selection on hybrids and the biological variables that shape such selection have hampered progress in this area. We discuss what is known about the mechanisms that drive changes in ancestry in the genome after hybridization, highlight major unresolved questions, and discuss their implications for the predictability of genome evolution after hybridization. Introduction Recent evidence has shown that hybridization between species is common. Hybridization is widespread across the tree of life, spanning both ancient and recent timescales and a broad range of divergence levels between taxa [1–10]. This appreciation of the prevalence of hybridization has renewed interest among researchers in understanding its consequences. -
Hybrid Incompatibility Is Stronger in the Presence of Transposable Elements in the Drosophila Virilis Clade
bioRxiv preprint doi: https://doi.org/10.1101/753814; this version posted August 3, 2021. The copyright holder for this preprint (which was not certified by peer review) is the author/funder. All rights reserved. No reuse allowed without permission. Hybrid incompatibility is stronger in the presence of transposable elements in the Drosophila virilis clade Dean M. Castillo*,1 and Leonie C. Moyle* *Department of Biology, Indiana University, Bloomington IN 47405 1. Current address: School of Biological Sciences, University of Utah, Salt Lake City UT 84112 bioRxiv preprint doi: https://doi.org/10.1101/753814; this version posted August 3, 2021. The copyright holder for this preprint (which was not certified by peer review) is the author/funder. All rights reserved. No reuse allowed without permission. Abstract Mismatches between parental genomes in selfish elements are frequently hypothesized to underlie hybrid dysfunction and drive speciation. However, because the genetic basis of most hybrid incompatibilities is unknown, testing the contribution of selfish elements to reproductive isolation is difficult. Here we evaluated the role of transposable elements (TEs) in hybrid incompatibilities between Drosophila virilis and D. lummei by experimentally comparing hybrid incompatibility in a cross where active TEs are present in D. virilis (TE+) and absent in D. lummei, to a cross where these TEs are absent from both D. virilis (TE-) and D. lummei genotypes. Using genomic data, we confirmed copy number differences in TEs between the D. virilis (TE+) strain and a D. virilis (TE-) strain and D. lummei. We observed F1 postzygotic reproductive isolation specifically in the interspecific cross involving TE+ D. -
UNIVERSITY of CALIFORNIA Los Angeles Linking Human
UNIVERSITY OF CALIFORNIA Los Angeles Linking Human Evolutionary History to Phenotypic Variation A dissertation submitted in partial satisfaction of the requirements for the degree Doctor of Philosophy in Human Genetics by Arun Kumar Durvasula 2021 c Copyright by Arun Kumar Durvasula 2021 ABSTRACT OF THE DISSERTATION Linking Human Evolutionary History to Phenotypic Variation by Arun Kumar Durvasula Doctor of Philosophy in Human Genetics University of California, Los Angeles, 2021 Professor Kirk Edward Lohmueller, Co-chair Professor Sriram Sankararaman, Co-chair A central question in genetics asks how genetic variation influences phenotypic variation. The distribution of genetic variation in a population is reflective of the evolutionary forces that shape and maintain genetic diversity such as mutation, natural selection, and genetic drift. In turn, this genetic variation affects molecular phenotypes like gene expression and eventually leads to variation in complex traits. In my dissertation, I develop statistical methods and apply computational approaches to understand these dynamics in human populations. In the first chapter, I describe a statistical model for detecting the presence of archaic haplotypes in modern human populations without having access to a reference archaic genome. I apply this method to the genomes of individuals from Europe and find that I can recover segments of DNA inherited from Neanderthals as a result of archaic admixture. In the second chapter, I apply this method to the genomes of individuals from several African populations and find that approximately 7% of the genomes are inherited from an archaic species. Modeling of the site frequency spectrum suggests that the presence of these haplotypes is best explained by admixture with an unknown archaic hominin species. -
2020 Online Session Descriptions
Thursday, April 16 2:00 pm - 6:00 pm Mammalian Trainee Symposium Session Chairs: Fernando Pardo-Manuel de Villena, UNC Chapel Hill Linda Siracusa, Hackensack Meridian School of Medicine at Seton Hall University 538A 2:00 pm No more paywalls: cost-benefit analysis across scRNA-seq platforms reveals biological insight is reproducible at low sequencing depths. Kathryn McClelland, National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK/NIH) 882C 2:15 pm Control of target gene specificity in Wnt signaling by transcription factor interactions. Aravindabharathi Ramakrishnan, University of Michigan, Ann Arbor 2217C 2:30 pm Evolutionary genomics of centromeric satellites in House Mice (Mus). Uma Arora, The Jackson Laboratory 2:45 pm Reference quality mouse genomes reveal complete strain-specific haplotypes and novel functional loci. Mohab Helmy, EMBL-EBI 887B 3:00 pm Divergence in KRAB zinc finger proteins is associated with pluripotency spectrum in mouse embryonic stem cells. Candice Byers Jackson Laboratory 531C 3:15 pm Replicability and reproducibility of genetic analysis between different studies using identical Collaborative Cross inbred mice. UNC CHAPEL HILL 3:30 pm Proteomics reveals the role of translational regulation in ES cells. Selcan Aydin, The Jackson Laboratory for Mouse Genetics 563B 3:45 pm Super-Mendelian inheritance mediated by CRISPR–Cas9 in the female mouse germline. Hannah Grunwald, University of California San Diego 2103C 4:00 pm Gene Editing ELANE in Human Hematopoietic Stem and Progenitor Cells Reveals Variant Pathogenicity and Therapeutic Strategies for Severe Congenital Neutropenia. Shuquan Rao, Boston Childrens Hospital 4:15 pm Phase separation of YAP reorganizes genome topology for long-term YAP target gene expression. -
View / Open Thesis Final-Moore.Pdf
INCOMPATIBILITY AND SPECIATION WITHIN & BETWEEN SPECIES by HANNA MOORE A THESIS Presented to the Department of BIOLOGY and the Robert D. Clark Honors College in partial fulfillment of the requirements for the degree of Bachelor of Science June 2015 Acknowledgements I would like to use this space to thank and acknowledge all those who contributed their skill, knowledge, help, and mental and emotional support to make this thesis a reality. I thank Dr. Patrick Phillips for his mentorship and guidance in designing and carrying out this experiment, as well as his patience and support in helping me to analyze and synthesize my findings. I thank both Dr. Samantha Hopkins and Dr. Peter Wetherwax for their participation on my thesis committee and their general advising and support over the past couple of years. I would like to sincerely thank and acknowledge Valerie Haskins, Chris Hanson, and Addison Kaufman all of whom contributed many volunteered hours of their time in the lab helping me transfer, hatch off, and count the 71,335 worms and 277,850 eggs I analyzed (as well as the extras that weren’t used). I would like to sincerely thank both Miriam Rigby and Christine O’Connor for contributing their computational skills, time, and knowledge and making all of the data figures and edits possible. I thank John Willis and Janna Fierst for working to help me begin the genomics analysis that didn’t quite make it in time to be included. And lastly, but absolutely not least, I thank all of my friends and family who have feigned or expressed real interest in hearing about “my worms” and who have provided their support and encouragement throughout the past three years of data collection and the entire thesis process. -
The University of Chicago Leveraging Haplotype
THE UNIVERSITY OF CHICAGO LEVERAGING HAPLOTYPE-BASED INFERENCE TO DESCRIBE ADAPTATION AND SPECIATION A DISSERTATION SUBMITTED TO THE FACULTY OF THE DIVISION OF THE BIOLOGICAL SCIENCES AND THE PRITZKER SCHOOL OF MEDICINE IN CANDIDACY FOR THE DEGREE OF DOCTOR OF PHILOSOPHY DEPARTMENT OF ECOLOGY AND EVOLUTION BY JOEL HAVILAND SMITH CHICAGO, ILLINOIS JUNE 2018 TABLE OF CONTENTS LIST OF FIGURES . iv LIST OF TABLES . ix ACKNOWLEDGMENTS . xi ABSTRACT . xii 1 INTRODUCTION . 1 2 ESTIMATING TIME TO THE COMMON ANCESTOR FOR A BENEFI- CIAL ALLELE . 8 2.1 Abstract . .8 2.2 Introduction . .9 2.3 Model Description . 15 2.4 Inference . 21 2.5 Results . 23 2.5.1 Recombination Versus Mutation as a Source of Information . 27 2.5.2 Application to 1000 Genomes Data . 29 2.6 Discussion . 35 2.7 Materials and Methods . 43 3 ESTIMATING THE TIMING OF ADAPTIVE INTROGRESSION . 47 3.1 Abstract . 47 3.2 Introduction . 48 3.3 Coat Color Adaptation in North American Wolves . 50 3.4 High Altitude Adaptation in Tibetans . 55 3.5 Discussion . 58 4 EXPECTED PATTERNS OF LOCAL ANCESTRY IN A HYBRID ZONE 63 4.1 Abstract . 63 4.2 Introduction . 64 4.2.1 Two-Locus Genetic Incompatibilities . 68 4.3 Model Description . 71 4.3.1 Tract Length Distributions Under Neutral Admixture . 71 4.3.2 A Locus-Specific Tract Length Distribution With Selection . 73 4.4 Discussion . 95 ii 5 DO HELICONIUS BUTTERFLY SPECIES EXCHANGE MIMICRY ALLE- LES? . 99 5.1 Abstract . 99 5.2 Introduction . 100 5.3 Materials and Methods . 104 5.4 Results . -
Genetics of Hybrid Incompatibility Between Lycopersicon Esculentum and L
Copyright © 2005 by the Genetics Society of America DOI: 10.1534/genetics.104.029546 Genetics of Hybrid Incompatibility Between Lycopersicon esculentum and L. hirsutum Leonie C. Moyle*,1 and Elaine B. Graham† *Center for Population Biology and †Tomato Genetics Resource Center, University of California, Davis, California 95616 Manuscript received March 31, 2004 Accepted for publication September 30, 2004 ABSTRACT We examined the genetics of hybrid incompatibility between two closely related diploid hermaphroditic plant species. Using a set of near-isogenic lines (NILs) representing 85% of the genome of the wild species Lycopersicon hirsutum (Solanum habrochaites) in the genetic background of the cultivated tomato L. esculentum (S. lycopersicum), we found that hybrid pollen and seed infertility are each based on 5–11 QTL that individu- ally reduce hybrid fitness by 36–90%. Seed infertility QTL act additively or recessively, consistent with findings in other systems where incompatibility loci have largely been recessive. Genetic lengths of intro- gressed chromosomal segments explain little of the variation for hybrid incompatibility among NILs, arguing against an infinitesimal model of hybrid incompatibility and reinforcing our inference of a limited number of discrete incompatibility factors between these species. In addition, male (pollen) and other (seed) incompatibility factors are roughly comparable in number. The latter two findings contrast strongly with data from Drosophila where hybrid incompatibility can be highly polygenic and complex, and male sterility evolves substantially faster than female sterility or hybrid inviability. The observed differences between Lycopersicon and Drosophila might be due to differences in sex determination system, reproductive and mating biology, and/or the prevalence of sexual interactions such as sexual selection. -
Pheromonal Mechanisms of Reproductive Isolation in Xiphophorus
PHEROMONAL MECHANISMS OF REPRODUCTIVE ISOLATION IN XIPHOPHORUS AND THEIR HYBRIDS A Dissertation by CHRISTOPHER HOLLAND Submitted to the Office of Graduate and Professional Studies of Texas A&M University in partial fulfillment of the requirements for the degree of DOCTOR OF PHILOSOPHY Chair of Committee, Gil G. Rosenthal Committee Members, Michael Smotherman Kevin W. Conway Jessica L. Yorzinski Head of Department, Thomas McKnight December 2018 Major Subject: Biology Copyright 2018 Christopher Holland ABSTRACT Pheromones play an important role in conspecific mate preference across taxa. While the mechanisms underlying the pheromonal basis of reproductive isolation are well characterized in insects, we know far less about the mechanisms underlying the production and reception of chemical signals in vertebrates. In the genus Xiphophorus, conspecific mate recognition depends on female perception of male urine-borne pheromones. I focused on interspecific differences between the sympatric X. birchmanni and X. malinche, which form natural hybrid zones as a consequence of changes in water chemistry. First, I identify the organ of pheromone production and compounds comprising chemical signals. I localized pheromone production to the testis; testis extract elicited the same conspecific preference as signals generated by displaying males. I used solid phase extraction (SPE) in combination with high performance liquid chromatography (HPLC)/ mass spectrometry (MS) to characterize pheromone chemical composition. Analyzing HPLC/MS readouts for pure peaks with high relative intensity identified two compounds of interest, which were identified according to their fraction pattern and retention times and then individually assayed for their effect on female behavior. The ability to directly measure the pheromones with paired responses of female conspecific mate recognition gives insight into what specific components are important to female mate choice. -
Clusters of Incompatible Genotypes Evolve with Limited Dispersal
ORIGINAL RESEARCH published: 22 April 2015 doi: 10.3389/fgene.2015.00151 Clusters of incompatible genotypes evolve with limited dispersal Erin L. Landguth 1*, Norman A. Johnson 2 and Samuel A. Cushman 3 1 Computational Ecology Laboratory, Division of Biological Sciences, University of Montana, Missoula, MT, USA, 2 Department of Biology, Department of Environmental Conservation, and Graduate Program in Organismic and Evolutionary Biology, University of Massachusetts, Amherst, MA, USA, 3 Rocky Mountain Research Station, United States Forest Service, Flagstaff, AZ, USA Theoretical and empirical studies have shown heterogeneous selection to be the primary driver for the evolution of reproductively isolated genotypes in the absence of geographic barriers. Here, we ask whether limited dispersal alone can lead to the evolution of reproductively isolated genotypes despite the absence of any geographic barriers or heterogeneous selection. We use a spatially-explicit, individual-based, landscape genetics program to explore the influences of dispersal strategies on reproductive isolation. We simulated genetic structure in a continuously distributed population and across various dispersal strategies (ranging from short- to long-range individual Edited by: movement), as well as potential mate partners in entire population (ranging from 20 to Stéphane Joost, 5000 individuals). We show that short-range dispersal strategies lead to the evolution of École Polytechnique Fédérale de Lausanne, Switzerland clusters of reproductively isolated genotypes despite the absence of any geographic Reviewed by: barriers or heterogeneous selection. Clusters of genotypes that are reproductively Severine Vuilleumier, isolated from other clusters can persist when migration distances are restricted such University of Lausanne, Switzerland that the number of mating partners is below about 350 individuals. -
Autoimmunity: a Barrier to Gene Flow in Plants? Liza Gross | Doi:10.1371/Journal.Pbio.0050262
Autoimmunity: A Barrier to Gene Flow in Plants? Liza Gross | doi:10.1371/journal.pbio.0050262 Nearly 150 years after Darwin published The Origin of Species, evolutionary biologists are still working out the conditions and processes that give rise to new species. Central to the identity of a species—whether species exist in nature or as theoretical constructs, as some argue—is the ability to interbreed and produce fertile offspring. Several mechanisms can act as reproductive barriers, either before or after fertilization, to prevent gene fl ow between populations and set the stage for speciation. One postfertilization mechanism in plants, called hybrid necrosis, arises from interactions between genes that cause misshapen, yellow, or damaged leaves and stunted growth, much like an infection. Hybrid necrosis occurs in crosses within and between species, suggesting that similar evolutionary processes may be at work at different times as the genes of the interbreeding species drift apart. Conditions like hybrid necrosis, according to the classic Dobzhansky-Muller model of hybrid incompatibility, arise from deleterious interactions between genes inherited from the parents. As parental lineages diverge, the theory goes, each line evolves independent mutations that are harmless in the parent but prove detrimental when co-expressed in the hybrid. The evolutionary forces driving this divergence doi:10.1371/journal.pbio.0050262.g001 are not well understood, but adaptive evolution has been implicated in generating hybrid incompatibility, based on Incompatibilities between genes inherited from healthy parents (center) cause disorders like hybrid necrosis when combined in evidence that known incompatibility genes evolve rapidly. offspring, which develop yellowed misshapen leaves and stunted In a new study, Kirsten Bomblies et al.