Sex determination through X-Y heterogamety in Salix nigra.


Journal

Heredity
ISSN: 1365-2540
Titre abrégé: Heredity (Edinb)
Pays: England
ID NLM: 0373007

Informations de publication

Date de publication:
04 2021
Historique:
received: 21 04 2020
accepted: 14 12 2020
revised: 01 12 2020
pubmed: 30 1 2021
medline: 26 10 2021
entrez: 29 1 2021
Statut: ppublish

Résumé

The development of non-recombining sex chromosomes has radical effects on the evolution of discrete sexes and sexual dimorphism. Although dioecy is rare in plants, sex chromosomes have evolved repeatedly throughout the diversification of angiosperms, and many of these sex chromosomes are relatively young compared to those found in vertebrates. In this study, we designed and used a sequence capture array to identify a novel sex-linked region (SLR) in Salix nigra, a basal species in the willow clade, and demonstrated that this species has XY heterogamety. We did not detect any genetic overlap with the previously characterized ZW SLRs in willows, which map to a different chromosome. The S. nigra SLR is characterized by strong recombination suppression across a 2 MB region and an excess of low-frequency alleles, resulting in a low Tajima's D compared to the remainder of the genome. We speculate that either a recent bottleneck in population size or factors related to positive or background selection generated this differential pattern of Tajima's D on the X and autosomes. This discovery provides insights into factors that may influence the evolution of sex chromosomes in plants and contributes to a large number of recent observations that underscore their dynamic nature.

Identifiants

pubmed: 33510464
doi: 10.1038/s41437-020-00397-3
pii: 10.1038/s41437-020-00397-3
pmc: PMC8115673
doi:

Types de publication

Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, Non-P.H.S.

Langues

eng

Sous-ensembles de citation

IM

Pagination

630-639

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Auteurs

Brian J Sanderson (BJ)

Department of Biological Sciences, Texas Tech University, Lubbock, TX, 79409-3131, USA. brian@biologicallyrelevant.com.
Department of Biology, West Virginia University, Morgantown, WV, 26506-6057, USA. brian@biologicallyrelevant.com.

Guanqiao Feng (G)

Department of Biological Sciences, Texas Tech University, Lubbock, TX, 79409-3131, USA.

Nan Hu (N)

Department of Biological Sciences, Texas Tech University, Lubbock, TX, 79409-3131, USA.

Craig H Carlson (CH)

Horticulture Section, School of Integrative Plant Science, Cornell University, Cornell AgriTech, Geneva, NY, 14456, USA.

Lawrence B Smart (LB)

Horticulture Section, School of Integrative Plant Science, Cornell University, Cornell AgriTech, Geneva, NY, 14456, USA.

Ken Keefover-Ring (K)

Departments of Botany and Geography, University of Wisconsin-Madison, Madison, WI, 53706, USA.

Tongming Yin (T)

Key Laboratory of Tree Genetics and Biotechnology of Jiangsu Province and Education Department of China, Nanjing Forestry University, Nanjing, China.

Tao Ma (T)

Key Laboratory of Bio-Resource and Eco-Environment of Ministry of Education & College of Life Sciences, Sichuan University, Chengdu, 610065, China.

Jianquan Liu (J)

Key Laboratory of Bio-Resource and Eco-Environment of Ministry of Education & College of Life Sciences, Sichuan University, Chengdu, 610065, China.
State Key Laboratory of Grassland Agro-Ecosystem, Institute of Innovation Ecology & College of Life Sciences, Lanzhou University, Lanzhou, 730000, China.

Stephen P DiFazio (SP)

Department of Biology, West Virginia University, Morgantown, WV, 26506-6057, USA.

Matthew S Olson (MS)

Department of Biological Sciences, Texas Tech University, Lubbock, TX, 79409-3131, USA.

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