Evidence map›Paper›PMID 31286854›Full record

ArticleBMC genomics2019

Systematic identification of intergenic long-noncoding RNAs in mouse retinas using full-length isoform sequencing.

Ying Wan, Xiaoyang Liu, Dongwang Zheng, Yuying Wang, Huan Chen, Xiaofeng Zhao, Guoqing Liang, Dongliang Yu, Lin Gan

Open access · goldAbstract read
In one paragraph

Article in BMC genomics, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
2.8field-weighted citation impact, top 9% 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

16 citing papers in PubMed, 57 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Epigenetic regulation of retinal development.Epigenetics & chromatin · 2021
    Review
  14. AFrontiers in genetics · 2021
    Article
  15. Article
  16. 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

9 authors at 3 institutions in 2 countries.

Ying WanCollege of Life and Environmental Sciences, Hangzhou Normal University, Hangzhou, China.
Xiaoyang LiuCollege of Life and Environmental Sciences, Hangzhou Normal University, Hangzhou, China.
Dongwang ZhengZhejiang Academy of Medical Sciences, Hangzhou, China.
Yuying WangCollege of Life and Environmental Sciences, Hangzhou Normal University, Hangzhou, China.
Huan ChenKey Laboratory of microbiological technology and Bioinformatics in Zhejiang Province, Hangzhou, China.
Xiaofeng ZhaoCollege of Life and Environmental Sciences, Hangzhou Normal University, Hangzhou, China.
Guoqing LiangCollege of Life and Environmental Sciences, Hangzhou Normal University, Hangzhou, China.
Dongliang YuCollege of Life and Environmental Sciences, Hangzhou Normal University, Hangzhou, China. yudl@hznu.edu.cn.ORCID http://orcid.org/0000-0003-3626-0296
Lin GanDepartment of Ophthalmology and Flaum Eye Institute, University of Rochester, Rochester, NY, 14642, USA. lin_gan@urmc.rochester.edu.
Hangzhou Normal University · CNUniversity of Rochester Medical Center · USZhejiang Academy of Medical Sciences · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundA great mass of long noncoding RNAs (lncRNAs) have been identified in mouse genome and increasing evidences in the last decades have revealed their crucial roles in diverse biological processes. Nevertheless, the biological roles of lncRNAs in the mouse retina remains largely unknown due to the lack of a comprehensive annotation of lncRNAs expressed in the retina.

resultsIn this study, we applied the long-reads sequencing strategy to unravel the transcriptomes of developing mouse retinas and identified a total of 940 intergenic lncRNAs (lincRNAs) in embryonic and neonatal retinas, including about 13% of them were transcribed from unannotated gene loci. Subsequent analysis revealed that function of lincRNAs expressed in mouse retinas were closely related to the physiological roles of this tissue, including 90 lincRNAs that were differentially expressed after the functional loss of key regulators of retinal ganglion cell (RGC) differentiation. In situ hybridization results demonstrated the enrichment of three class IV POU-homeobox genes adjacent lincRNAs (linc-3a, linc-3b and linc-3c) in ganglion cell layer and indicated they were potentially RGC-specific.

conclusionsIn summary, this study systematically annotated the lincRNAs expressed in embryonic and neonatal mouse retinas and implied their crucial regulatory roles in retinal development such as RGC differentiation.

Indexed as

GenomicsSequence Analysis, RNAAnimalsMiceRetinaRetinal Ganglion CellsRNA IsoformsRNA, Long NoncodingRNA IsoformsRNA, Long Noncoding

Identifiers

PMID31286854
PMCPMC6615288
OpenAlexW2957663557

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.