<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Yue J</submitter><funding>Fujian Agriculture and Forestry University</funding><funding>Biotechnology and Biological Sciences Research Council</funding><funding>JSPS</funding><funding>Japan Society for the Promotion of Science</funding><pagination>2504-2514.e3</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC7617815</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>33(12)</volume><pubmed_abstract>White campion (Silene latifolia, Caryophyllaceae) was the first vascular plant where sex chromosomes were discovered. This species is a classic model for studies on plant sex chromosomes due to presence of large, clearly distinguishable X and Y chromosomes that originated de novo about 11 million years ago (mya), but lack of genomic resources for this relatively large genome (∼2.8 Gb) remains a significant hurdle. Here we report S. latifolia female genome assembly integrated with sex-specific genetic maps of this species, focusing on sex chromosomes and their evolution. The analysis reveals a highly heterogeneous recombination landscape with strong reduction in recombination rate in the central parts of all chromosomes. Recombination on the X chromosome in female meiosis primarily occurs at the very ends, and over 85% of the X chromosome length is located in a massive (∼330 Mb) gene-poor, rarely recombining pericentromeric region (Xpr). The results indicate that the non-recombining region on the Y chromosome (NRY) initially evolved in a relatively small (∼15 Mb), actively recombining region at the end of the q-arm, possibly as a result of inversion on the nascent X chromosome. The NRY expanded about 6 mya via linkage between the Xpr and the sex-determining region, which may have been caused by expanding pericentromeric recombination suppression on the X chromosome. These findings shed light on the origin of sex chromosomes in S. latifolia and yield genomic resources to assist ongoing and future investigations into sex chromosome evolution.</pubmed_abstract><journal>Current biology : CB</journal><pubmed_title>The origin and evolution of sex chromosomes, revealed by sequencing of the Silene latifolia female genome.</pubmed_title><pmcid>PMC7617815</pmcid><funding_grant_id>JP21KK0128</funding_grant_id><funding_grant_id>JP22H05071</funding_grant_id><funding_grant_id>BB/P009808/1</funding_grant_id><pubmed_authors>Xie W</pubmed_authors><pubmed_authors>Kan B</pubmed_authors><pubmed_authors>Kazama Y</pubmed_authors><pubmed_authors>Zhang X</pubmed_authors><pubmed_authors>Ming R</pubmed_authors><pubmed_authors>Zhang S</pubmed_authors><pubmed_authors>Xu X</pubmed_authors><pubmed_authors>Filatov DA</pubmed_authors><pubmed_authors>Yue J</pubmed_authors><pubmed_authors>Krasovec M</pubmed_authors></additional><is_claimable>false</is_claimable><name>The origin and evolution of sex chromosomes, revealed by sequencing of the Silene latifolia female genome.</name><description>White campion (Silene latifolia, Caryophyllaceae) was the first vascular plant where sex chromosomes were discovered. This species is a classic model for studies on plant sex chromosomes due to presence of large, clearly distinguishable X and Y chromosomes that originated de novo about 11 million years ago (mya), but lack of genomic resources for this relatively large genome (∼2.8 Gb) remains a significant hurdle. Here we report S. latifolia female genome assembly integrated with sex-specific genetic maps of this species, focusing on sex chromosomes and their evolution. The analysis reveals a highly heterogeneous recombination landscape with strong reduction in recombination rate in the central parts of all chromosomes. Recombination on the X chromosome in female meiosis primarily occurs at the very ends, and over 85% of the X chromosome length is located in a massive (∼330 Mb) gene-poor, rarely recombining pericentromeric region (Xpr). The results indicate that the non-recombining region on the Y chromosome (NRY) initially evolved in a relatively small (∼15 Mb), actively recombining region at the end of the q-arm, possibly as a result of inversion on the nascent X chromosome. The NRY expanded about 6 mya via linkage between the Xpr and the sex-determining region, which may have been caused by expanding pericentromeric recombination suppression on the X chromosome. These findings shed light on the origin of sex chromosomes in S. latifolia and yield genomic resources to assist ongoing and future investigations into sex chromosome evolution.</description><dates><release>2023-01-01T00:00:00Z</release><publication>2023 Jun</publication><modification>2026-06-01T12:02:47.398Z</modification><creation>2026-04-08T12:00:34.799Z</creation></dates><accession>S-EPMC7617815</accession><cross_references><pubmed>37290443</pubmed><doi>10.1016/j.cub.2023.05.046</doi></cross_references></HashMap>