Evidence map›Paper›PMID 35668612›Full record

ArticleGenome biology and evolution2022

The Spruce Budworm Genome: Reconstructing the Evolutionary History of Antifreeze Proteins.

Catherine Béliveau, Patrick Gagné, Sandrine Picq, Oksana Vernygora, Christopher I Keeling, Kristine Pinkney, Daniel Doucet, Fayuan Wen, J Spencer Johnston, Halim Maaroufi and 16 more

Open access · goldAbstract read
In one paragraph

Article in Genome biology and evolution, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
1.4field-weighted citation impact, top 20% of its field
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

8 citing papers in PubMed, 8 citations in OpenAlex.

  1. Article
  2. Article
  3. Ontogenetic variability of the Siberian silk moth,Frontiers in insect science · 2026
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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

26 authors at 9 institutions in 3 countries.

Catherine BéliveauLaurentian Forestry Centre, Natural Resources Canada, Quebec City, Quebec, Canada.
Patrick GagnéLaurentian Forestry Centre, Natural Resources Canada, Quebec City, Quebec, Canada.
Sandrine PicqLaurentian Forestry Centre, Natural Resources Canada, Quebec City, Quebec, Canada.
Oksana VernygoraDepartment of Entomology, University of Kentucky, Lexington, Kentucky, USA.
Christopher I KeelingLaurentian Forestry Centre, Natural Resources Canada, Quebec City, Quebec, Canada.
Kristine PinkneyGreat Lakes Forestry Centre, Natural Resources Canada, Sault Ste. Marie, Ontario, Canada.
Daniel DoucetGreat Lakes Forestry Centre, Natural Resources Canada, Sault Ste. Marie, Ontario, Canada.
Fayuan WenGreat Lakes Forestry Centre, Natural Resources Canada, Sault Ste. Marie, Ontario, Canada.
J Spencer JohnstonDepartment of Entomology, Texas A&M University, 2475 College Station, Texas, USA.
Halim MaaroufiInstitut de biologie intégrative et des systèmes, Université Laval, Quebec City, Quebec, Canada.
Brian BoyleInstitut de biologie intégrative et des systèmes, Université Laval, Quebec City, Quebec, Canada.
Jérôme LarocheInstitut de biologie intégrative et des systèmes, Université Laval, Quebec City, Quebec, Canada.
Ken DewarQuantitative Life Sciences, McGill University, Montreal, Quebec, Canada.
Nikoleta JureticResearch Institute of the McGill University Health Centre, Montreal, Quebec, Canada.
Gwylim BlackburnPacific Forestry Centre, Natural Resources Canada, Victoria, British Columbia, Canada.
Audrey NisoleLaurentian Forestry Centre, Natural Resources Canada, Quebec City, Quebec, Canada.
Bryan BrunetOttawa Research and Development Centre, Agriculture and Agri-Food Canada, Ottawa, Ontario, Canada.
Marcelo BrandaoLaboratório de Biologia Integrativa e Sistêmica - CBMEG/UNICAMP, Campinas, Brazil.
Lisa LumleyAlberta Biodiversity Monitoring Institute, University of Alberta, Edmonton, Alberta, Canada.
Jun DuanLaurentian Forestry Centre, Natural Resources Canada, Quebec City, Quebec, Canada.
Guoxing QuanGreat Lakes Forestry Centre, Natural Resources Canada, Sault Ste. Marie, Ontario, Canada.
Christopher J LucarottiAtlantic Forestry Centre, Natural Resources Canada, Fredericton, New Brunswick, Canada.
Amanda D RoeGreat Lakes Forestry Centre, Natural Resources Canada, Sault Ste. Marie, Ontario, Canada.
Felix A H SperlingDepartment of Biological Sciences, University of Alberta, Edmonton, Alberta, Canada.
Roger C LevesqueInstitut de biologie intégrative et des systèmes, Université Laval, Quebec City, Quebec, Canada.
Michel CussonLaurentian Forestry Centre, Natural Resources Canada, Quebec City, Quebec, Canada.ORCID 0000-0003-1541-6052
Natural Resources Canada · CAUniversité Laval · CAUniversity of Alberta · CAAgriculture and Agri-Food Canada · CAMcGill University · CAMcGill University Health Centre · CATexas A&M University · USUniversidade Estadual de Campinas (UNICAMP) · BRUniversity of Kentucky · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Insects have developed various adaptations to survive harsh winter conditions. Among freeze-intolerant species, some produce "antifreeze proteins" (AFPs) that bind to nascent ice crystals and inhibit further ice growth. Such is the case of the spruce budworm, Choristoneura fumiferana (Lepidoptera: Tortricidae), a destructive North American conifer pest that can withstand temperatures below -30°C. Despite the potential importance of AFPs in the adaptive diversification of Choristoneura, genomic tools to explore their origins have until now been limited. Here we present a chromosome-scale genome assembly for C. fumiferana, which we used to conduct comparative genomic analyses aimed at reconstructing the evolutionary history of tortricid AFPs. The budworm genome features 16 genes homologous to previously reported C. fumiferana AFPs (CfAFPs), 15 of which map to a single region on chromosome 18. Fourteen of these were also detected in five congeneric species, indicating Choristoneura AFP diversification occurred before the speciation event that led to C. fumiferana. Although budworm AFPs were previously considered unique to the genus Choristoneura, a search for homologs targeting recently sequenced tortricid genomes identified seven CfAFP-like genes in the distantly related Notocelia uddmanniana. High structural similarity between Notocelia and Choristoneura AFPs suggests a common origin, despite the absence of homologs in three related tortricids. Interestingly, one Notocelia AFP formed the C-terminus of a "zonadhesin-like" protein, possibly representing the ancestral condition from which tortricid AFPs evolved. Future work should clarify the evolutionary path of AFPs between Notocelia and Choristoneura and assess the role of the "zonadhesin-like" protein as precursor of tortricid AFPs.

Indexed as

antifreeze proteinsChoristoneura fumiferanacomparative genomicsevolutionary historygenome assemblyTortricidae

Identifiers

PMID35668612
PMCPMC9210311
OpenAlexW4281653918

What Socratic holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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 Socratic graph.