Evidence map›Paper›PMID 42010124›Full record

ArticleNeurochemical research2026

MicroRNA and Proteomic Landscape of Brain Development.

Abhishek Jauhari, Sanjeev Kumar Yadav, Tanisha Singh, Sanjay Yadav

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In one paragraph

Article in Neurochemical research, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
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0citing papers in PubMed
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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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

4 authors.

Abhishek JauhariDevelopmental Toxicology Laboratory, Systems Toxicology and Health Risk Assessment Group, CSIR- Indian Institute of Toxicology Research (CSIR-IITR) Vishvigyan Bhawan, 31 Mahatma Gandhi Marg, Lucknow, Uttar Pradesh, 226001, India. abj33@pitt.edu.
Sanjeev Kumar YadavDevelopmental Toxicology Laboratory, Systems Toxicology and Health Risk Assessment Group, CSIR- Indian Institute of Toxicology Research (CSIR-IITR) Vishvigyan Bhawan, 31 Mahatma Gandhi Marg, Lucknow, Uttar Pradesh, 226001, India.
Tanisha SinghDevelopmental Toxicology Laboratory, Systems Toxicology and Health Risk Assessment Group, CSIR- Indian Institute of Toxicology Research (CSIR-IITR) Vishvigyan Bhawan, 31 Mahatma Gandhi Marg, Lucknow, Uttar Pradesh, 226001, India.
Sanjay YadavDevelopmental Toxicology Laboratory, Systems Toxicology and Health Risk Assessment Group, CSIR- Indian Institute of Toxicology Research (CSIR-IITR) Vishvigyan Bhawan, 31 Mahatma Gandhi Marg, Lucknow, Uttar Pradesh, 226001, India. biochem_sanjay@aiimsrbl.edu.in.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Brain development is a complex and continuous process that begins during the gestation period and peeks in adolescence. This process unfolds in multiple phases and involves cellular events like cell proliferation, migration, axonal and dendritic outgrowth, apoptosis, synapse formation, myelination, and synaptic pruning. Each of these developmental processes is tightly regulated by intricate layers of gene expression. MicroRNAs (miRNAs) play a crucial role in regulating gene expression post-transcriptionally. Due to their ability to regulate multiple genes with a single miRNA and a single gene with multiple miRNAs, miRNAs are particularly well-suited to orchestrate gene expression during brain development. In this study, we utilized rat brain samples from various developmental stages: gestation day 15 (GD15), 0-days, 1-week, 3-weeks, 6-weeks, 12-weeks, and 1-year, to investigate the dynamic changes in brain development. We analyzed the global miRNA expression and proteomic profile at each time point using rat miRNA TaqMan Low Density Arrays and LC–MS/MS, respectively. Our analysis revealed that miRNA and protein expression are tightly regulated throughout brain development from GD15 to 1 year. Interestingly, the patterns of global expression of miRNAs and proteins are dramatically different in GD15 and 0-day. Some miRNAs exhibited stage-specific expression patterns, while others were consistently expressed at higher levels across the entire developmental period. Notably, the expression levels of certain miRNAs, including the miR-29 family, miR-34 family, miR-338, and miR-219, were found to increase as brain development progressed. These miRNAs had minimal expression at GD15 and reached their highest levels at 12-weeks or 1-year. Conversely, miR-296, miR-217, miR-20b-3p, and miR-214 exhibited peak expression at GD15, with levels decreasing by 12-weeks and 1-year. In addition, we examined phase-specific protein expression profiles using mass spectrometry to further complement our findings.

Indexed as

BrainMicroRNAsProteomicsAnimalsFemaleGene Expression Regulation, DevelopmentalNeurodevelopmentRatsRats, Sprague-DawleyMicroRNAsBrain developmentMicroRNAsmiR-219miR-29 familymiR-338miR-34 family

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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.