Evidence map›Paper›PMID 40667345›Full record

ArticlebioRxiv : the preprint server for biology2025

CrebA regulation of secretory capacity: Genome-wide transcription profiling coupled with in vivo DNA binding studies.

D J Jackson, D Peng, S A Shinde, A Holenarasipura, P Cahan, D J Andrew

Abstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 2025. 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
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
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

5 · Who and what money

Authors and funding

6 authors.

D J JacksonEqual first authors.
D PengEqual first authors.
S A ShindeDepartment of Cell Biology, The Johns Hopkins University School of Medicine.
A HolenarasipuraDepartment of Cell Biology, The Johns Hopkins University School of Medicine.
P CahanDepartment of Biomedical Engineering, The Johns Hopkins University School of Medicine.ORCID 0000-0003-3652-2540
D J AndrewDepartment of Cell Biology, The Johns Hopkins University School of Medicine.ORCID 0000-0003-1051-6935

Funding

FORMATION OF THE DROSOPHILA SALIVARY GLANDR01DE013899 · NIDCR · JOHNS HOPKINS UNIVERSITY · PI Deborah J Andrew · 2001 to 2026
$11.2M
NIDCR NIH HHS R01 DE013899
6 · The paper itself

Abstract

DNA binding assays, expression analyses, and binding site mutagenesis revealed that the Drosophila CrebA transcription factor (TF) boosts secretory capacity in the embryonic salivary gland (SG) through direct regulation of secretory pathway component genes (SPCGs). The mammalian orthologues of CrebA, the Creb3L-family of leucine zipper TFs, not only activate SPCG expression in a variety of mammalian tissues but can also activate SPCG expression in Drosophila embryos, suggesting a highly conserved role for this family of proteins in boosting secretory capacity. However, in vivo assays reveal that CrebA binds far more genes than it regulates, and it remains unclear what distinguishes functional binding. It is also unclear if CrebA is the major factor driving SPCG gene expression in all Drosophila embryonic tissues and/or if CrebA also regulates other tissue-specific functions. Thus, we did single cell RNA sequencing (scRNA-seq) of wild-type (WT) and

Indexed as

Chromatin Immunoprecipitation and sequencing (ChIP-Seq)CrebAsalivary glandsecretionSecretory pathway component genes (SPCGs)single cell RNA seq (scRNA-Seq)

Identifiers

PMID40667345
PMCPMC12262295

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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.