A punctuated burst of massive genomic rearrangements by chromosome shattering and the origin of non-marine annelids DOI Creative Commons
Rosa Fernández, Carlos Vargas-Chávez, Lisandra Benítez-Álvarez

и другие.

Research Square (Research Square), Год журнала: 2024, Номер unknown

Опубликована: Май 21, 2024

Abstract The genomic basis of cladogenesis and adaptive evolutionary change has intrigued biologists for decades. unique insights from a genome-level perspective have revealed striking pattern conserved macrosynteny across huge distances in animals, yet progress many lineages been hampered by the absence data. Here, we show that origin Clitellata, clade composed most freshwater all terrestrial species phylum Annelida, coincided with an unprecedented genome-wide scrambling event resulted massive loss between marine annelids clitellates. This complete breakdown chromosome-level relationships on just one short branch is unlike any other known genome rearrangement, instead resembles chromosome shattering reassembly seen chromoanagenesis. These punctuated rearrangements included formation neocentromeres newly-acquired transposable elements, preceded further period reshaping events including whole duplications macrosyntenic reshuffling clitellate lineages, potentially triggered genes involved stability or homeostasis cell division. Notably, while these broke short-range interactions observed (including Hox), they were reformed as long-range Our study provides evidence via chromoanagenesis leading not only to new animal lineage - ‘hopeful monster’ but also changes facilitating colonisation habitats.

Язык: Английский

Structural Variants and Speciation: Multiple Processes at Play DOI
Emma L. Berdan, Thomas G. Aubier, Salvatore Cozzolino

и другие.

Cold Spring Harbor Perspectives in Biology, Год журнала: 2023, Номер 16(3), С. a041446 - a041446

Опубликована: Дек. 5, 2023

Emma L. Berdan1,2, Thomas G. Aubier3,4, Salvatore Cozzolino5, Rui Faria6,7, Jeffrey Feder8, Mabel D. Giménez9,10, Mathieu Joron11, Jeremy B. Searle12 and Claire Mérot13 1Department of Marine Sciences, Gothenburg University, 40530, Sweden 2Bioinformatics Core, Department Biostatistics, Harvard T.H. Chan School Public Health, Medical School, Boston, Massachusetts 02115, USA 3Laboratoire Évolution & Diversité Biologique, Université Paul Sabatier Toulouse III, UMR 5174, CNRS/IRD, 31077 Toulouse, France 4Department Biology, University North Carolina at Chapel Hill, 27599, 5Department Naples Federico II, Complesso Universitario di Monte S. Angelo, 80126 Napoli, Italia 6CIBIO, Centro de Investigação em Biodiversidade e Recursos Genéticos, InBIO, Laboratório Associado, Universidade do Porto, Vairão, Portugal 7BIOPOLIS Program in Genomics, Biodiversity Land Planning, CIBIO, 4485-661 8Department Biological Notre Dame, Indiana 46556, 9Consejo Nacional Investigaciones Científicas y Técnicas (CONICET), Instituto Genética Humana Misiones (IGeHM), Parque la Salud Provincia "Dr. Ramón Madariaga," N3300KAZ Posadas, Misiones, Argentina 10Facultad Ciencias Exactas, Químicas Naturales, Universidad N3300LQH 11Centre d'Ecologie Fonctionnelle et Evolutive, Montpellier, CNRS, EPHE, IRD, 12Department Ecology Evolutionary Cornell Ithaca, New York 14853, 13CNRS, 6553 Ecobio, OSUR, Rennes, 35000 Correspondence: claire.merot{at}gmail.com; emma.berdan{at}gmail.com

Язык: Английский

Процитировано

20

Sex‐biased gene content is associated with sex chromosome turnover in Danaini butterflies DOI Creative Commons
Pablo Mora, Monika Hospodářská, Anna Voleníková

и другие.

Molecular Ecology, Год журнала: 2024, Номер 33(24)

Опубликована: Янв. 5, 2024

Sex chromosomes play an outsized role in adaptation and speciation, thus deserve particular attention evolutionary genomics. In particular, fusions between sex autosomes can produce neo-sex chromosomes, which offer important insights into the dynamics of chromosomes. Here, we investigate origin previously reported Danaus chromosome within tribe Danaini. We assembled annotated genomes Tirumala septentrionis (subtribe Danaina), Ideopsis similis (Amaurina), Idea leuconoe (Euploeina) Lycorea halia (Itunina) identified their Z-linked scaffolds. found that resulting from fusion a Z autosome corresponding to Melitaea cinxia (McChr) 21 arose common ancestor Danaina, Amaurina Euploina. also two additional as W further fused with synteny block McChr31 I. independent occurred ancestral McChr12 L. halia. tested possible sexually antagonistic selection turnover by analysing genomic distribution sex-biased genes The McChr21 involved are significantly enriched female- male-biased genes, respectively, could have hypothetically facilitated fixation This suggests sexual antagonism Lepidoptera. neo-Z both appear fully compensated somatic tissues, but extent dosage compensation for varies across tissues species.

Язык: Английский

Процитировано

8

Mechanisms of Intrinsic Postzygotic Isolation: From Traditional Genic and Chromosomal Views to Genomic and Epigenetic Perspectives DOI
Radka Reifová, S. Lorena Ament‐Velásquez, Yann Bourgeois

и другие.

Cold Spring Harbor Perspectives in Biology, Год журнала: 2023, Номер 15(10), С. a041607 - a041607

Опубликована: Сен. 11, 2023

Radka Reifová1, S. Lorena Ament-Velásquez2, Yann Bourgeois3, Jenn Coughlan4, Jonna Kulmuni5,6, Agnieszka P. Lipinska7,8, Genta Okude9, Laurie Stevison10, Kohta Yoshida9 and Jun Kitano9 1Department of Zoology, Faculty Science, Charles University, 128 00 Prague, Czech Republic 2Department Stockholm 106 91 Stockholm, Sweden 3DIADE, University Montpellier, CIRAD, IRD, 34090 France 4Department Ecology & Evolutionary Biology, Yale New Haven, Connecticut 06520, USA 5Institute for Biodiversity Ecosystem Dynamics, Department Population Amsterdam, 1012 The Netherlands 6Organismal Biology Research Programme, Helsinki, 00100 Finland 7Department Algal Development Evolution, Max Planck Institute 72076 Tuebingen, Germany 8CNRS, UMR 8227, Integrative Marine Models, Sorbonne Université, Station Biologique de Roscoff, 29680 9Department Genomics National Genetics, Mishima, Shizuoka 411-8540, Japan 10Department Biological Sciences, Auburn Auburn, Alabama 36849, Correspondence: radka.reifova{at}natur.cuni.cz; jkitano{at}nig.ac.jp

Язык: Английский

Процитировано

14

A punctuated burst of massive genomic rearrangements by chromosome shattering and the origin of non-marine annelids DOI Creative Commons
Carlos Vargas-Chávez, Lisandra Benítez-Álvarez, Gemma I. Martínez‐Redondo

и другие.

bioRxiv (Cold Spring Harbor Laboratory), Год журнала: 2024, Номер unknown

Опубликована: Май 20, 2024

The genomic basis of cladogenesis and adaptive evolutionary change has intrigued biologists for decades. unique insights gained from a genome-level perspective have revealed striking pattern conserved macrosynteny within chromosomes across huge phylogenetic distances in animals, yet progress many lineages been hampered by the absence data. Here, we show that tectonics genome evolution clitellates, clade composed most freshwater all terrestrial species phylum Annelida, is characterised extensive genome-wide scrambling resulted massive loss between marine annelids to point ancient bilaterian linkage groups (ie, genes inherited as block phyla) are fully disrupted. These rearrangements included formation putative neocentromeres with newly acquired transposable elements, preceded further period reshaping events including whole-genome duplications macrosyntenic reshuffling clitellate lineages, potentially triggered involved stability homeostasis cell division. Notably, while these broke short-range interactions observed Hox annelids, they were reformed long-range clitellates. led relocation new chimeric genetic both which may contributed adaptation clitellates environments. Our findings provide evidence at 2D 3D levels, suggest synteny not limit structural this animal lineage. study thus suggests landscape Clitellata rare burst changes ended long persists large distances.

Язык: Английский

Процитировано

5

Combining Molecular, Macroevolutionary, and Macroecological Perspectives on the Generation of Diversity DOI
Lindell Bromham

Cold Spring Harbor Perspectives in Biology, Год журнала: 2024, Номер 16(9), С. a041453 - a041453

Опубликована: Март 19, 2024

Charles Darwin presented a unified process of diversification driven by the gradual accumulation heritable variation. The growth in DNA databases and increase genomic sequencing, combined with advances molecular phylogenetic analyses, gives us an opportunity to realize Darwin's vision, connecting generation variation lineages. rate evolution is correlated across animals plants, but relationship between genome change speciation complex: Mutation rates evolve response life history niche; substitution are influenced mutation, selection, population size; acquisition reproductive isolation vary populations; traits, niches, distribution can influence rates. connection mutation one part complex varied story speciation, which has theoretical importance for understanding biodiversity also practical impacts on use understand dynamics over macroevolutionary timescales.

Язык: Английский

Процитировано

4

Chromosomal fusions and large-scale inversions are key features for adaptation in Arctic codfish species DOI Creative Commons
Siv Nam Khang Hoff, Marius F. Maurstad, Ole K. Tørresen

и другие.

bioRxiv (Cold Spring Harbor Laboratory), Год журнала: 2024, Номер unknown

Опубликована: Июнь 28, 2024

Abstract The evolutionary impact of structural variants, such as chromosomal inversions, is well documented, especially for their role in local adaptation high gene flow systems. However, the other genomic rearrangements like fusions, fissions, and translocations still relatively unexplored. Here we present six chromosome-level Gadid reference genomes non-migratory Atlantic cod ( Gadus morhua ) i.e., Norwegian coastal (NCC), haddock (Melanogrammus aeglefinus), burbot Lota lota ), European hake Merluccius merluccius two keystone Arctic codfishes: polar Boreogadus saida Arctogadus glacialis ). Within a comparative genomics framework, uncovered several lineage-specific resulting reduced number chromosomes compared to ancestral state cold-water adapted codfishes. identified fusions were not homologous, indicating that they originate from independent events. Additionally, partly overlapping inversions between species detected. Using smaller population dataset, degree conservation some (including breakpoint regions), suggesting these regions are under selection, potentially importance. With use genome assemblies, demonstrate how large reorganizations likely play important roles speciation processes thus, particular freezing environmental conditions. Moreover, observe massive rearrangement events can take place across short time scales.

Язык: Английский

Процитировано

3

The Primula edelbergii S‐locus is an example of a jumping supergene DOI Creative Commons
Giacomo Potente, Narjes Yousefi, Barbara Keller

и другие.

Molecular Ecology Resources, Год журнала: 2024, Номер 24(6)

Опубликована: Июнь 30, 2024

Abstract Research on supergenes, non‐recombining genomic regions housing tightly linked genes that control complex phenotypes, has recently gained prominence in genomics. Heterostyly, a floral heteromorphism promoting outcrossing several angiosperm families, is controlled by the S ‐locus supergene. The been studied primarily closely related Primula species and, more recently, other groups independently evolved heterostyly. However, it remains unknown whether genetic architecture and composition of are maintained among share common origin heterostyly subsequently diverged across larger time scales. To address this research gap, we present chromosome‐scale genome assembly edelbergii , shares same with veris (whose characterized) but from 18 million years ago. Comparative analyses between these two allowed us to show, for first time, can ‘jump’ (i.e. translocate) chromosomes maintaining its function controlling Additionally, found four were conserved reshuffled within supergene, seemingly without affecting their expression, thus could not detect changes explaining lack self‐incompatibility P. . Furthermore, confirmed undergoing degeneration. Finally, investigated evolutionary history Ericales terms whole duplications transposable element accumulation. In summary, our work provides valuable resource comparative aimed at investigating genetics pivotal role supergenes shaping evolution phenotypes.

Язык: Английский

Процитировано

3

Chromosomal inversions and their impact on insect evolution DOI

Igor V Sharakhov,

Maria V. Sharakhova

Current Opinion in Insect Science, Год журнала: 2024, Номер 66, С. 101280 - 101280

Опубликована: Окт. 5, 2024

Язык: Английский

Процитировано

3

Hierarchical architecture of neo-sex chromosomes and accelerated adaptive evolution in tortricid moths DOI
Fangyuan Yang, Jun‐Li Cao, Petr Nguyen

и другие.

Genome Research, Год журнала: 2025, Номер 35(1), С. 66 - 77

Опубликована: Янв. 1, 2025

Sex chromosomes can expand through fusion with autosomes, thereby acquiring unique evolutionary patterns. In butterflies and moths (Lepidoptera), these sex chromosome–autosome (SA) fusions occur relatively frequently, suggesting possible advantages. Here, we investigated how SA affects chromosome features molecular evolution in leafroller (Lepidoptera: Tortricidae). Phylogenomic analysis showed that Tortricidae diverged ∼124 million years ago, accompanied by an between the Merian elements M(20 + 17) MZ. contrast to partial autosomal fusions, fused neo-Z Chromosome developed a hierarchical architecture, which three exhibit heterogeneous sequence Specifically, M17 part had distinct base composition chromatin domains. Unlike M20 MZ, was expressed at same levels as autosomes both sexes, compensating for lost gene dosage females. Concurrently, drove hotspot, accelerating of several genes related ecological adaptation (e.g., ABCC s) facilitating divergence closely species, whereas undercompensated did not show such effect. Thus, accelerated under novel pattern compensation may have favored adaptive radiation this group. This study demonstrates association karyotype variant explains recurrent Lepidoptera.

Язык: Английский

Процитировано

0

Centromere diversity and its evolutionary impacts on plant karyotypes and plant reproduction DOI Creative Commons
Stefan Steckenborn, André Marques

New Phytologist, Год журнала: 2025, Номер 245(5), С. 1879 - 1886

Опубликована: Янв. 6, 2025

Summary Karyotype changes are a formidable evolutionary force by directly impacting cross‐incompatibility, gene dosage, genetic linkage, chromosome segregation, and meiotic recombination landscape. These often arise spontaneously commonly detected within plant lineages, even between closely related accessions. One element that can influence drastic karyotype after only one (or few) generations is the alteration of centromere position, number, distribution, or its strength. Here, we briefly explore how these different configurations result in rearrangements, reproduction recombination.

Язык: Английский

Процитировано

0