Evidence map›Paper›PMID 38776329›Full record

ArticleGenome biology and evolution2024

Genome Evolution and Introgression in the New Zealand mud Snails Potamopyrgus estuarinus and Potamopyrgus kaitunuparaoa.

Peter D Fields, Joseph R Jalinsky, Laura Bankers, Kyle E McElroy, Joel Sharbrough, Chelsea Higgins, Mary Morgan-Richards, Jeffrey L Boore, Maurine Neiman, John M Logsdon

Abstract read
In one paragraph

Article in Genome biology and evolution, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

3 citing papers in PubMed.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

10 authors.

Peter D FieldsDepartment of Environmental Sciences, Zoology, University of Basel, Basel 4051, Switzerland.ORCID 0000-0003-2959-2524
Joseph R JalinskyDepartment of Biology, University of Iowa, Iowa City, IA, USA.ORCID 0000-0003-2922-0130
Laura BankersDepartment of Biology, University of Iowa, Iowa City, IA, USA.ORCID 0000-0001-6433-9263
Kyle E McElroyDepartment of Ecology, Evolution, and Organismal Biology, Iowa State University, Ames, IA, USA.ORCID 0000-0001-9581-2535
Joel SharbroughDepartment of Biology, New Mexico Institute of Mining and Technology, Socorro, NM, USA.ORCID 0000-0002-3642-1662
Chelsea HigginsDepartment of Biology, University of Iowa, Iowa City, IA, USA.ORCID 0000-0002-1400-7161
Mary Morgan-RichardsSchool of Natural Sciences, Massey University Manawatū, Palmerston North, New Zealand.ORCID 0000-0002-3913-9814
Jeffrey L BoorePhenome Health, Seattle, WA, USA.ORCID 0000-0001-6751-4549
Maurine NeimanDepartment of Biology, University of Iowa, Iowa City, IA, USA.ORCID 0000-0002-1543-8115
John M LogsdonDepartment of Biology, University of Iowa, Iowa City, IA, USA.ORCID 0000-0002-0031-462X

Funding

TRAINING IN MECHANISMS OF PARASITISMT32AI007511 · NIAID · UNIVERSITY OF IOWA · PI BUTLER, NOAH SULLIVAN, WEBER, MARY · 1996 to 2025
$8.1M
Colorado State UniversityMassey University RM22261National Science Foundation MCB-1122176NIAID NIH HHS T32 AI007511University of Colorado Boulder 2201538
6 · The paper itself

Abstract

We have sequenced, assembled, and analyzed the nuclear and mitochondrial genomes and transcriptomes of Potamopyrgus estuarinus and Potamopyrgus kaitunuparaoa, two prosobranch snail species native to New Zealand that together span the continuum from estuary to freshwater. These two species are the closest known relatives of the freshwater species Potamopyrgus antipodarum-a model for studying the evolution of sex, host-parasite coevolution, and biological invasiveness-and thus provide key evolutionary context for understanding its unusual biology. The P. estuarinus and P. kaitunuparaoa genomes are very similar in size and overall gene content. Comparative analyses of genome content indicate that these two species harbor a near-identical set of genes involved in meiosis and sperm functions, including seven genes with meiosis-specific functions. These results are consistent with obligate sexual reproduction in these two species and provide a framework for future analyses of P. antipodarum-a species comprising both obligately sexual and obligately asexual lineages, each separately derived from a sexual ancestor. Genome-wide multigene phylogenetic analyses indicate that P. kaitunuparaoa is likely the closest relative to P. antipodarum. We nevertheless show that there has been considerable introgression between P. estuarinus and P. kaitunuparaoa. That introgression does not extend to the mitochondrial genome, which appears to serve as a barrier to hybridization between P. estuarinus and P. kaitunuparaoa. Nuclear-encoded genes whose products function in joint mitochondrial-nuclear enzyme complexes exhibit similar patterns of nonintrogression, indicating that incompatibilities between the mitochondrial and the nuclear genome may have prevented more extensive gene flow between these two species.

Indexed as

PhylogenySnailsAnimalsEvolution, MolecularGenetic IntrogressionGenomeGenome, MitochondrialNew Zealandgastropod evolutionintrogressionPotamopyrgus

Identifiers

PMID38776329
PMCPMC11110935

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.