Evidence map›Paper›PMID 38088586›Full record

ArticleAdvanced science (Weinheim, Baden-Wurttemberg, Germany)2024

The miR-669a-5p/G3BP/HDAC6/AKAP12 Axis Regulates Primary Cilia Length.

Weina Wang, Xuyao Dai, Yue Li, Mo Li, Zongqi Chi, Xiaoyu Hu, Zhenshan Wang

Open access · goldAbstract read
In one paragraph

Article in Advanced science (Weinheim, Baden-Wurttemberg, Germany), 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
1.9field-weighted citation impact, top 12% 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

6 citing papers in PubMed, 6 citations in OpenAlex.

  1. Article
  2. Article
  3. Histone Deacetylase 6 (HDAC6) in Ciliopathies: Emerging Insights and Therapeutic Implications.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2025
    Review
  4. NAdvanced science (Weinheim, Baden-Wurttemberg, Germany) · 2025
    Article
  5. The miR-669a-5p/G3BP/HDAC6/AKAP12 Axis Regulates Primary Cilia Length.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2024
    Article
  6. Review
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

7 authors at 2 institutions in 1 country.

Weina WangSchool of Life Sciences, Institute of Life Science and Green Development, Hebei University, Baoding, 071002, China.
Xuyao DaiSchool of Life Sciences, Institute of Life Science and Green Development, Hebei University, Baoding, 071002, China.
Yue LiSchool of Life Sciences, Institute of Life Science and Green Development, Hebei University, Baoding, 071002, China.
Mo LiSchool of Public Health, Hebei University, Baoding, 071000, China.
Zongqi ChiSchool of Public Health, Hebei University, Baoding, 071000, China.
Xiaoyu HuSchool of Life Sciences, Institute of Life Science and Green Development, Hebei University, Baoding, 071002, China.ORCID 0000-0002-6030-0019
Zhenshan WangSchool of Life Sciences, Institute of Life Science and Green Development, Hebei University, Baoding, 071002, China.ORCID 0000-0002-1478-1739
Hebei University · CNBaoding University · CN

Funding

Hebei Province Graduate Innovation Funding Project CXZZBS2021010Hebei Province Graduate Innovation Funding Project CXZZSS2022002High-Level Talents Research Start-Up Project of Hebei University 521100222049Institute of Life Science and Green Development, Hebei University 050001-5000019National Natural Science Foundation of China 32070567National Natural Science Foundation of China 32202840
6 · The paper itself

Abstract

Primary cilia are conserved organelles in most mammalian cells, acting as "antennae" to sense external signals. Maintaining a physiological cilium length is required for cilium function. MicroRNAs (miRNAs) are potent gene expression regulators, and aberrant miRNA expression is closely associated with ciliopathies. However, how miRNAs modulate cilium length remains elusive. Here, using the calcium-shock method and small RNA sequencing, a miRNA is identified, namely, miR-669a-5p, that is highly expressed in the cilia-enriched noncellular fraction. It is shown that miR-669a-5p promotes cilium elongation but not cilium formation in cultured cells. Mechanistically, it is demonstrated that miR-669a-5p represses ras-GTPase-activating protein SH3-domain-binding protein (G3BP) expression to inhibit histone deacetylase 6 (HDAC6) expression, which further upregulates A-kinase anchor protein 12 (AKAP12) expression. This effect ultimately blocks cilia disassembly and leads to greater cilium length, which can be restored to wild-type lengths by either upregulating HDAC6 or downregulating AKAP12. Collectively, these results elucidate a previously unidentified miR-669a-5p/G3BP/HDAC6/AKAP12 signaling pathway that regulates cilium length, providing potential pharmaceutical targets for treating ciliopathies.

Indexed as

CiliopathiesMicroRNAsA Kinase Anchor ProteinsAnimalsCiliaHistone Deacetylase 6MammalsA Kinase Anchor ProteinsHistone Deacetylase 6MicroRNAsAKAP12G3BPsHDAC6miR-669a-5pprimary cilia

Identifiers

PMID38088586
PMCPMC10853727
OpenAlexW4389673178

What OpenQuestion 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 OpenQuestion graph.