Evidence map›Paper›PMID 38365592›Full record

ArticleBMC genomics2024

Distinct regulatory networks control toxin gene expression in elapid and viperid snakes.

Cassandra M Modahl, Summer Xia Han, Jory van Thiel, Candida Vaz, Nathan L Dunstan, Seth Frietze, Timothy N W Jackson, Stephen P Mackessy, R Manjunatha Kini

Open access · goldAbstract read
In one paragraph

Article in BMC genomics, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
5.0field-weighted citation impact, top 5% 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

10 citing papers in PubMed, 9 citations in OpenAlex.

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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

9 authors at 4 institutions in 3 countries.

Cassandra M ModahlDepartment of Biological Sciences, Faculty of Science, National University of Singapore, Singapore, Singapore. Cassandra.Modahl@lstmed.ac.uk.
Summer Xia HanDepartment of Biological Sciences, Faculty of Science, National University of Singapore, Singapore, Singapore.
Jory van ThielCentre for Snakebite Research and Interventions, Liverpool School of Tropical Medicine, Liverpool, U.K.
Candida VazHuman Development, Institute for Clinical Sciences (SICS), Agency for Science, Technology and Research (A*STAR), Singapore, Singapore.
Nathan L DunstanVenom Supplies, Tanunda, South Australia, Australia.
Seth FrietzeDepartment of Biomedical and Health Sciences, University of Vermont, Burlington, VT, U.S.A.
Timothy N W JacksonAustralian Venom Research Unit, Department of Biochemistry and Pharmacology, University of Melbourne, Melbourne, Australia.
Stephen P MackessyDepartment of Biological Sciences, University of Northern Colorado, Greeley, CO, U.S.A.
R Manjunatha KiniDepartment of Biological Sciences, Faculty of Science, National University of Singapore, Singapore, Singapore. dbskinim@nus.edu.sg.
National University of Singapore · SGLeiden University · NLSingapore Institute for Clinical Sciences · SGUniversity of Melbourne · AU

Funding

Faculty of Science, National University of Singapore N/A
6 · The paper itself

Abstract

backgroundVenom systems are ideal models to study genetic regulatory mechanisms that underpin evolutionary novelty. Snake venom glands are thought to share a common origin, but there are major distinctions between venom toxins from the medically significant snake families Elapidae and Viperidae, and toxin gene regulatory investigations in elapid snakes have been limited. Here, we used high-throughput RNA-sequencing to profile gene expression and microRNAs between active (milked) and resting (unmilked) venom glands in an elapid (Eastern Brown Snake, Pseudonaja textilis), in addition to comparative genomics, to identify cis- and trans-acting regulation of venom production in an elapid in comparison to viperids (Crotalus viridis and C. tigris).

resultsAlthough there is conservation in high-level mechanistic pathways regulating venom production (unfolded protein response, Notch signaling and cholesterol homeostasis), there are differences in the regulation of histone methylation enzymes, transcription factors, and microRNAs in venom glands from these two snake families. Histone methyltransferases and transcription factor (TF) specificity protein 1 (Sp1) were highly upregulated in the milked elapid venom gland in comparison to the viperids, whereas nuclear factor I (NFI) TFs were upregulated after viperid venom milking. Sp1 and NFI cis-regulatory elements were common to toxin gene promoter regions, but many unique elements were also present between elapid and viperid toxins. The presence of Sp1 binding sites across multiple elapid toxin gene promoter regions that have been experimentally determined to regulate expression, in addition to upregulation of Sp1 after venom milking, suggests this transcription factor is involved in elapid toxin expression. microRNA profiles were distinctive between milked and unmilked venom glands for both snake families, and microRNAs were predicted to target a diversity of toxin transcripts in the elapid P. textilis venom gland, but only snake venom metalloproteinase transcripts in the viperid C. viridis venom gland. These results suggest differences in toxin gene posttranscriptional regulation between the elapid P. textilis and viperid C. viridis.

conclusionsOur comparative transcriptomic and genomic analyses between toxin genes and isoforms in elapid and viperid snakes suggests independent toxin regulation between these two snake families, demonstrating multiple different regulatory mechanisms underpin a venomous phenotype.

Indexed as

CrotalusMicroRNAsToxins, BiologicalVenomous SnakesViperidaeAnimalsElapidaeElapid VenomsHumansSnake VenomsTranscription FactorsTranscriptomeElapid VenomsMicroRNAsSnake VenomsToxins, BiologicalTranscription FactorsEpigeneticsFront-fanged snakesToxin promotersVenom delivery systems

Identifiers

PMID38365592
PMCPMC10874052
OpenAlexW4391886506

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LicenceCC BY
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Registered trials

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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.