Evidence map›Paper›PMID 35399503›Full record

ArticleFrontiers in cell and developmental biology2022

Origin and Evolution of the Multifaceted Adherens Junction Component Plekha7.

Antonis Kourtidis, Bryan Dighera, Alyssa Risner, Rob Hackemack, Nikolas Nikolaidis

Open access · goldAbstract read
In one paragraph

Article in Frontiers in cell and developmental biology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.8field-weighted citation impact, top 32% 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

5 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

5 authors at 2 institutions in 1 country.

Antonis KourtidisDepartment of Regenerative Medicine and Cell Biology, Medical University of South Carolina, Charleston, SC, United States.
Bryan DigheraDepartment of Biological Science, Center for Applied Biotechnology Studies, Center for Computational and Applied Mathematics, College of Natural Sciences and Mathematics, California State University, Fullerton, Fullerton, CA, United States.
Alyssa RisnerDepartment of Regenerative Medicine and Cell Biology, Medical University of South Carolina, Charleston, SC, United States.
Rob HackemackDepartment of Biological Science, Center for Applied Biotechnology Studies, Center for Computational and Applied Mathematics, College of Natural Sciences and Mathematics, California State University, Fullerton, Fullerton, CA, United States.
Nikolas NikolaidisDepartment of Biological Science, Center for Applied Biotechnology Studies, Center for Computational and Applied Mathematics, College of Natural Sciences and Mathematics, California State University, Fullerton, Fullerton, CA, United States.
California State University, Fullerton · USMedical University of South Carolina · US

Funding

South Carolina IDeA Networks of Biomedical Research (SC INBRE V)P20GM103499 · NIGMS · UNIVERSITY OF SOUTH CAROLINA AT COLUMBIA · PI EDIE C GOLDSMITH · 2012 to 2026
$61.0M
South Carolina Clinical & Translational Research Institute (SCTR)UL1TR001450 · NCATS · MEDICAL UNIVERSITY OF SOUTH CAROLINA · PI BRADY, KATHLEEN T., FLUME, PATRICK A · 2015 to 2024
$41.1M
The role of SMAD1 and SATB2 in colon patterningP20GM130457 · NIGMS · MEDICAL UNIVERSITY OF SOUTH CAROLINA · PI Evan R Delgado · 2020 to 2026
$18.7M
Proteomics CoreP30DK123704 · NIDDK · MEDICAL UNIVERSITY OF SOUTH CAROLINA · PI Garth R Swanson · 2020 to 2026
$8.8M
South Carolina Clinical & Translational Research Institute (SCTR)TL1TR001451 · NCATS · MEDICAL UNIVERSITY OF SOUTH CAROLINA · PI FEGHALI-BOSTWICK, CAROL A. · 2015 to 2024
$4.6M
Epithelial adherens junctions regulate colon cell behavior through RNAi and lncRNAsR01DK124553 · NIDDK · MEDICAL UNIVERSITY OF SOUTH CAROLINA · PI KOURTIDIS, ANTONIS · 2021 to 2024
$1.3M
Digestive Disease Training ProgramT32DK124191 · NIDDK · MEDICAL UNIVERSITY OF SOUTH CAROLINA · PI STEPHEN A DUNCAN, Antonis Kourtidis · 2021 to 2026
$1.0M
Racial disparity in triple-negative breast cancer lipid metabolismP20CA253251 · NCI · CALIFORNIA STATE UNIVERSITY FULLERTON · PI TOLMASKY, MARCELO E · 2021 to 2024
$895k
Interaction between HspA1A, a seventy-kDa heat shock protein, and lipids in stressed cellsSC3GM121226 · NIGMS · CALIFORNIA STATE UNIVERSITY FULLERTON · PI NIKOLAIDIS, NIKOLAS · 2017 to 2024
$843k
PIWI - Transposon regulation by epithelial adherens junctionsR21CA246233 · NCI · MEDICAL UNIVERSITY OF SOUTH CAROLINA · PI KOURTIDIS, ANTONIS · 2020 to 2021
$384k
NCATS NIH HHS TL1 TR001451NCATS NIH HHS UL1 TR001450NCI NIH HHS P20 CA253251NCI NIH HHS R21 CA246233NIDDK NIH HHS P30 DK123704NIDDK NIH HHS R01 DK124553NIDDK NIH HHS T32 DK124191NIGMS NIH HHS P20 GM103499NIGMS NIH HHS P20 GM130457NIGMS NIH HHS SC3 GM121226
6 · The paper itself

Abstract

Plekha7 is a key adherens junction component involved in numerous functions in mammalian cells. Plekha7 is the most studied member of the PLEKHA protein family, which includes eight members with diverse functions. However, the evolutionary history of Plekha7 remains unexplored. Here, we outline the phylogeny and identify the origins of this gene and its paralogs. We show that Plekha7, together with Plekha4, Plekha5, and Plekha6, belong to a subfamily that we name PLEKHA4/5/6/7. This subfamily is distinct from the other Plekha proteins, which form two additional separate subfamilies, namely PLEKHA1/2 and PLEKHA3/8. Sequence, phylogenetic, exon-intron organization, and syntenic analyses reveal that the PLEKHA4/5/6/7 subfamily is represented by a single gene in invertebrates, which remained single in the last common ancestor of all chordates and underwent gene duplications distinctly in jawless and jawed vertebrates. In the latter species, a first round of gene duplications gave rise to the Plekha4/7 and Plekha5/6 pairs and a second round to the four extant members of the subfamily. These observations are consistent with the 1R/2R hypothesis of vertebrate genome evolution. Plekha7 and Plekha5 also exist in two copies in ray-finned fishes, due to the Teleostei-specific whole genome duplication. Similarities between the vertebrate Plekha4/5/6/7 members and non-chordate sequences are restricted to their N-terminal PH domains, whereas similarities across the remaining protein molecule are only sporadically found among few invertebrate species and are limited to the coiled-coil and extreme C-terminal ends. The vertebrate Plekha4/5/6/7 proteins contain extensive intrinsically disordered domains, which are topologically and structurally conserved in all chordates, but not in non-chordate invertebrates. In summary, our study sheds light on the origins and evolution of Plekha7 and the PLEKHA4/5/6/7 subfamily and unveils new critical information suitable for future functional studies of this still understudied group of proteins.

Indexed as

chordatesgnathostomesphylogenyPLEKHAPlekha4Plekha5Plekha6Plekha7

Identifiers

PMID35399503
PMCPMC8983885
OpenAlexW4221125082

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.