ArticlePlants (Basel, Switzerland)2025
Genomic Survey of Genes Encoding Major Intrinsic Proteins (MIPs) and Their Response to Arsenite Stress in Pepper (
Article in Plants (Basel, Switzerland), 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
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.
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.
Who cites it
0 citing papers in PubMed.
No citing paper in PubMed yet.
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
10 authors.
Funding
Abstract
Major intrinsic proteins (MIPs) are a super family of proteins that mediate the bidirectional concentration-dependent flux of water in particularly small solutes in fraction and some metalloids across the cell membrane. This article reports the genome-wide study of pepper genes encoding MIPs and their expression analysis. Using a bioinformatics homology search, 48 CAMIPs were identified on the genome of pepper. A total of 48 MIPs were further divided in sub classes as 22 CATIPs, 15 CAPIPs, 10 CANIPs, and 1 CASIP. The 48 Pepper MIP encoding genes were mapped on the 12 pepper chromosomes. CAMIP synteny analysis exhibited 17 duplicated genes, and these were clustered into eight tandem duplicated regions on pepper chromosomes. The tissue-specific expression of MIPs based on RNA-Seq showed certain CANIPs, CATIPs, and CAPIPs were highly expressed in roots, while some CATIPs and CASIPs were expressed in stem as well. As(III), at 0.5 and 1 mM, was applied to pepper plants, where 1 mM significantly reduced leaf chlorophyll content, leaf nitrogen content, and root length. To see which CAMIPs participate in As(III) transport, we tested the response of genes encoding MIPs to As(III) through qRT-PCR. As(III) uptake was observed in both shoot and root samples treated with 0.5 mM and 1 mM As(III) for 12 h and 24 h because of MIPs' quantitative response through qRT-PCR. Most of the MIPs were down-regulated in response to both levels of As(III); besides CANIPs, there were CATIPs and CAPIPs up-regulated in response to higher concentrations of As(III) in the roots and shoot, which suggests the involvement of CAMIPs in the uptake as well as detoxification mechanism in pepper against As(III). Unlike prokaryotes, plant MIPs have diverse selectivity for arsenite and other solutes. Our study provides important insights into the arsenite uptake and detoxification, offering a foundation for further functional and stress-tolerance studies.
Indexed as
Identifiers
What OpenQuestion holds
Registered trials
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.