Evidence map›Paper›PMID 36212145›Full record

ArticleFrontiers in genetics2022

miR-1306 induces cell apoptosis by targeting BMPR1B gene in the ovine granulosa cells.

Anwar Abdurahman, Wusimanjiang Aierken, Fei Zhang, Rahmantay Obulkasim, Jueken Aniwashi, Ablat Sulayman

Open access · goldAbstract read
In one paragraph

Article in Frontiers in genetics, 2022. 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
2.8field-weighted citation impact, top 8% 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, 14 citations in OpenAlex.

  1. Article
  2. Article
  3. ELK1 regulates BMPR1B transcriptional activity in ovine granulosa cells.Frontiers in cell and developmental biology · 2025
    Article
  4. Article
  5. Article
  6. Article
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

6 authors at 6 institutions in 1 country.

Anwar AbdurahmanShenzhen Key Laboratory of Marine Bioresources and Ecology, College of Life Sciences and Oceanography, Shenzhen University, Shenzhen, China.
Wusimanjiang AierkenThe Fifth Affiliate Hospital of Xinjiang Medical University, Urumqi, China.
Fei ZhangAnimal Diseases Control and Prevention Centre of Xinjiang Uygur Autonomous Region, Urumqi, China.
Rahmantay ObulkasimIli Kazak Autonomous Prefecture Institute of Animal Science, Ili, China.
Jueken AniwashiCollege of Animal Science and Technology, Xinjiang Agricultural University, Urumqi, China.
Ablat SulaymanInstitute of Animal Husbandry, Xinjiang Academy of Animal Science, Urumqi, China.
Animal Science Research Institute · CNBeijing Institute of Optoelectronic Technology · CNXinjiang Academy of Animal Science · CNXinjiang Agricultural University · CNXinjiang Medical University · CNXinjiang Uygur Autonomous Region Disease Prevention and Control Center · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Bone morphogenetic protein receptor type-1B (BMPR1B) is one of the major gene for sheep prolificacy. However, few studies investigated its regulatory region. In this study, we reported that miR-1306 is a direct inhibitor of BMPR1B gene in the ovine granulosa cells (ovine GCs). We detected a miRNA response element of miR-1306 in the 3' untranslated region of the ovine BMPR1B gene. Luciferase assay showed that the ovine BMPR1B gene is a direct target of miR-1306. qPCR and western blotting revealed that miR-1306 reduces the expression of BMPR1B mRNA and protein in the ovine granulosa cells. Furthermore, miR-1306 promoted cell apoptosis by suppressing BMPR1B expression in the ovine granulosa cells. Overall, our results suggest that miR-1306 is an epigenetic regulator of BMPR1B, and may serve as a potential target to improve the fecundity of sheep.

Indexed as

apoptosisBMPR1Bgranulosa cellmiR-1306sheep

Identifiers

PMID36212145
PMCPMC9539929
OpenAlexW4296838115

What OpenQuestion holds

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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.