Genetic variation in rare and common plants

被引:247
|
作者
Cole, CT [1 ]
机构
[1] Univ Minnesota, Div Sci & Math, Morris, MN 56267 USA
关键词
rare plants; conservation genetics; isozymes; monomorphism;
D O I
10.1146/annurev.ecolsys.34.030102.151717
中图分类号
Q14 [生态学(生物生态学)];
学科分类号
071012 ; 0713 ;
摘要
Isozyme variation in 247 plant species is summarized as 57 generic-level comparisons of rare and common species. All species-level measures of variation (P-s, A(s), AP(s), H-es) and mean population-level measures (P-p, A(p), AP(p), H-ep, and H-o) show reductions significant at the p < 0.001 level, but F-IS and F-ST did not differ significantly, reflecting the similarity of breeding system in congeneric species and disparate ranges often sampled for rare and common species. The reduction in gene flow (Nm) among populations of rare species was significant when estimated from F-ST, but not when estimated from private alleles. Species monomorphic for isozymes are predominantly endemic and self-fertile. Although census populations of virtually all rare species are higher than levels at which theory would predict genetic erosion, and higher than levels protected by the U.S. Endangered Species Act (ESA), rare plants evidently have more significant reductions in genetic variation and gene flow than have been recognized previously.
引用
收藏
页码:213 / 237
页数:25
相关论文
共 50 条
  • [1] DISSECTING THE CONTRIBUTIONS OF RARE AND COMMON GENETIC VARIATION TO NEURODEVELOPMENTAL OUTCOMES
    Dinneen, Thomas
    Molloy, Ciara J.
    Cliquet, Freddy
    Leblond, Claire S.
    Bourgeron, Thomas
    Cooke, Jennifer
    Loth, Eva
    Buitelaar, Jan K.
    Lopez, Lorna M.
    Gallagher, Louise
    EUROPEAN NEUROPSYCHOPHARMACOLOGY, 2023, 75 : S253 - S253
  • [3] Integrating common and rare genetic variation in diverse human populations
    Altshuler, David M.
    Gibbs, Richard A.
    Peltonen, Leena
    Dermitzakis, Emmanouil
    Schaffner, Stephen F.
    Yu, Fuli
    Bonnen, Penelope E.
    de Bakker, Paul I. W.
    Deloukas, Panos
    Gabriel, Stacey B.
    Gwilliam, Rhian
    Hunt, Sarah
    Inouye, Michael
    Jia, Xiaoming
    Palotie, Aarno
    Parkin, Melissa
    Whittaker, Pamela
    Chang, Kyle
    Hawes, Alicia
    Lewis, Lora R.
    Ren, Yanru
    Wheeler, David
    Muzny, Donna Marie
    Barnes, Chris
    Darvishi, Katayoon
    Hurles, Matthew
    Korn, Joshua M.
    Kristiansson, Kati
    Lee, Charles
    McCarroll, Steven A.
    Nemesh, James
    Keinan, Alon
    Montgomery, Stephen B.
    Pollack, Samuela
    Price, Alkes L.
    Soranzo, Nicole
    Gonzaga-Jauregui, Claudia
    Anttila, Verneri
    Brodeur, Wendy
    Daly, Mark J.
    Leslie, Stephen
    McVean, Gil
    Moutsianas, Loukas
    Nguyen, Huy
    Zhang, Qingrun
    Ghori, Mohammed J. R.
    McGinnis, Ralph
    McLaren, William
    Takeuchi, Fumihiko
    Grossman, Sharon R.
    NATURE, 2010, 467 (7311) : 52 - 58
  • [4] Rare and Common Genetic Variation Underlying Atrial Fibrillation Risk
    Vad, Oliver B.
    Monfort, Laia M.
    Paludan-Mueller, Christian
    Kahnert, Konstantin
    Diederichsen, Soren Z.
    Andreasen, Laura
    Lotta, Luca A.
    Nielsen, Jonas B.
    Lundby, Alicia
    Svendsen, Jesper H.
    Olesen, Morten S.
    JAMA CARDIOLOGY, 2024, 9 (08) : 732 - 740
  • [5] GENETIC MATERNAL EFFECT, ULTRA-RARE, RARE, AND COMMON VARIATION CONTRIBUTE TO THE GENETIC RISK ARCHITECTURE OF OCD
    Mahjani, Behrang
    JOURNAL OF THE AMERICAN ACADEMY OF CHILD AND ADOLESCENT PSYCHIATRY, 2022, 61 (10): : S296 - S296
  • [6] Analysis of common genetic variation and rare CNVs in the Australian Autism Biobank
    Yap, Chloe X.
    Alvares, Gail A.
    Henders, Anjali K.
    Lin, Tian
    Wallace, Leanne
    Farrelly, Alaina
    McLaren, Tiana
    Berry, Jolene
    Vinkhuyzen, Anna A. E.
    Trzaskowski, Maciej
    Zeng, Jian
    Yang, Yuanhao
    Cleary, Dominique
    Grove, Rachel
    Hafekost, Claire
    Harun, Alexis
    Holdsworth, Helen
    Jellett, Rachel
    Khan, Feroza
    Lawson, Lauren
    Leslie, Jodie
    Frenk, Mira Levis
    Masi, Anne
    Mathew, Nisha E.
    Muniandy, Melanie
    Nothard, Michaela
    Visscher, Peter M.
    Dawson, Paul A.
    Dissanayake, Cheryl
    Eapen, Valsamma
    Heussler, Helen S.
    Whitehouse, Andrew J. O.
    Wray, Naomi R.
    Gratten, Jacob
    MOLECULAR AUTISM, 2021, 12 (01)
  • [7] Common and Rare Coding Genetic Variation Underlying the Electrocardiographic PR Interval
    Lin, Honghuang
    van Setten, Jessica
    Smith, Albert V.
    Bihlmeyer, Nathan A.
    Warren, Helen R.
    Brody, Jennifer A.
    Radmanesh, Farid
    Hall, Leanne
    Grarup, Niels
    Mueller-Nurasyid, Martina
    Boutin, Thibaud
    Verweij, Niek
    Lin, Henry J.
    Li-Gao, Ruifang
    van den Berg, Marten E.
    Marten, Jonathan
    Weiss, Stefan
    Prins, Bram P.
    Haessler, Jeffrey
    Lyytikainen, Leo-Pekka
    Mei, Hao
    Harris, Tamara B.
    Launer, Lenore J.
    Li, Man
    Alonso, Alvaro
    Soliman, Elsayed Z.
    Connell, John M.
    Huang, Paul L.
    Weng, Lu-Chen
    Jameson, Heather S.
    Hucker, William
    Hanley, Alan
    Tucker, Nathan R.
    Chen, Yii-Der Ida
    Bis, Joshua C.
    Rice, Kenneth M.
    Sitlani, Colleen M.
    Kors, Jan A.
    Xie, Zhijun
    Wen, Chengping
    Magnani, Jared W.
    Nelson, Christopher P.
    Kanters, Jorgen K.
    Sinner, Moritz F.
    Strauch, Konstantin
    Peters, Annette
    Waldenberger, Melanie
    Meitinger, Thomas
    Bork-Jensen, Jette
    Pedersen, Oluf
    CIRCULATION-GENOMIC AND PRECISION MEDICINE, 2018, 11 (05): : e002037
  • [8] THE GENETIC DISSECTION OF BIPOLAR DISORDER: FROM COMMON TO RARE RISK VARIATION
    Zandi, Peter
    Kelsoe, John
    McMahon, Francis
    EUROPEAN NEUROPSYCHOPHARMACOLOGY, 2017, 27 : S128 - S128
  • [9] Analysis of common genetic variation and rare CNVs in the Australian Autism Biobank
    Chloe X. Yap
    Gail A. Alvares
    Anjali K. Henders
    Tian Lin
    Leanne Wallace
    Alaina Farrelly
    Tiana McLaren
    Jolene Berry
    Anna A. E. Vinkhuyzen
    Maciej Trzaskowski
    Jian Zeng
    Yuanhao Yang
    Dominique Cleary
    Rachel Grove
    Claire Hafekost
    Alexis Harun
    Helen Holdsworth
    Rachel Jellett
    Feroza Khan
    Lauren Lawson
    Jodie Leslie
    Mira Levis Frenk
    Anne Masi
    Nisha E. Mathew
    Melanie Muniandy
    Michaela Nothard
    Peter M. Visscher
    Paul A. Dawson
    Cheryl Dissanayake
    Valsamma Eapen
    Helen S. Heussler
    Andrew J. O. Whitehouse
    Naomi R. Wray
    Jacob Gratten
    Molecular Autism, 12
  • [10] The Value of Rare Genetic Variation in the Prediction of Common Obesity in European Ancestry Populations
    Wang, Zhe
    Choi, Shing Wan
    Chami, Nathalie
    Boerwinkle, Eric
    Fornage, Myriam
    Redline, Susan
    Bis, Joshua C.
    Brody, Jennifer A.
    Psaty, Bruce M.
    Kim, Wonji
    McDonald, Merry-Lynn N.
    Regan, Elizabeth A.
    Silverman, Edwin K.
    Liu, Ching-Ti
    Vasan, Ramachandran S.
    Kalyani, Rita R.
    Mathias, Rasika A.
    Yanek, Lisa R.
    Arnett, Donna K.
    Justice, Anne E.
    North, Kari E.
    Kaplan, Robert
    Heckbert, Susan R.
    de Andrade, Mariza
    Guo, Xiuqing
    Lange, Leslie A.
    Rich, Stephen S.
    Rotter, Jerome I.
    Ellinor, Patrick T.
    Lubitz, Steven A.
    Blangero, John
    Shoemaker, M. Benjamin
    Darbar, Dawood
    Gladwin, Mark T.
    Albert, Christine M.
    Chasman, Daniel I.
    Jackson, Rebecca D.
    Kooperberg, Charles
    Reiner, Alexander P.
    O'Reilly, Paul F.
    Loos, Ruth J. F.
    FRONTIERS IN ENDOCRINOLOGY, 2022, 13