Evidence map›Paper›PMID 29411102›Full record

ArticleHistochemistry and cell biology2018

1700108J01Rik and 1700101O22Rik are mouse testis-specific long non-coding RNAs.

Xiaohui Song, Chaw Kyi-Tha-Thu, Takami Takizawa, Banyar Than Naing, Toshihiro Takizawa

Abstract read
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In one paragraph

Article in Histochemistry and cell biology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
0.6field-weighted citation impact, top 40% 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

11 citing papers in PubMed, 25 citations in OpenAlex.

  1. Article
  2. Thousands of oscillating LncRNAs in the mouse testis.Computational and structural biotechnology journal · 2024
    Article
  3. Article
  4. Article
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  7. Review
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  11. Long noncoding RNAs: new insights in modulating mammalian spermatogenesis.Journal of animal science and biotechnology · 2020
    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

5 authors at 1 institution in 1 country.

Xiaohui SongDepartment of Molecular Medicine and Anatomy, Nippon Medical School, 1-1-5 Sendagi, Tokyo, 113-8602, Japan.
Chaw Kyi-Tha-ThuDepartment of Molecular Medicine and Anatomy, Nippon Medical School, 1-1-5 Sendagi, Tokyo, 113-8602, Japan.
Takami TakizawaDepartment of Molecular Medicine and Anatomy, Nippon Medical School, 1-1-5 Sendagi, Tokyo, 113-8602, Japan.
Banyar Than NaingDepartment of Molecular Medicine and Anatomy, Nippon Medical School, 1-1-5 Sendagi, Tokyo, 113-8602, Japan.
Toshihiro TakizawaDepartment of Molecular Medicine and Anatomy, Nippon Medical School, 1-1-5 Sendagi, Tokyo, 113-8602, Japan. t-takizawa@nms.ac.jp.ORCID http://orcid.org/0000-0002-9098-8387
Nippon Medical School · JP

Funding

Japan Society for the Promotion of Science 17K11256Japan Society for the Promotion of Science 17K16818Ministry of Education, Culture, Sports, Science and Technology the Strategic Research Foundation at Private Universities (2013-2017)
6 · The paper itself

Abstract

Long non-coding RNAs (lncRNAs; > 200 nucleotides in length) have attracted attention as fine-tuners of gene expression. However, little is known about the cell- and stage-specific expression pattern and function of lncRNAs in spermatogenesis. The purpose of this study was to identify mouse testis-associated lncRNAs using a combination of computational and experimental approaches. We first used the FANTOM5 database to survey lncRNA expression in the mouse testis and performed reverse transcription quantitative polymerase chain reaction (real-time PCR) and in situ hybridization (ISH) analyses. In silico analysis showed that most of the highly expressed lncRNAs in the adult mouse testis were testis-specific lncRNAs and were expressed at and following the initiation of spermatogenesis. We selected the antisense lncRNA 1700108J01Rik and long intergenic non-coding RNA 1700101O22Rik from the most highly expressed lncRNAs in the adult testis for further analysis. Real-time PCR analysis confirmed that 1700108J01Rik and 1700101O22Rik were specifically expressed in the testis. ISH analysis revealed that the two mouse-testis-specific lncRNAs were expressed exclusively in testicular germ cells in meiotic prophase and the round spermatid stage, which coincide with the period of transcriptional reactivation during spermatogenesis. The cytoplasmic distribution of these lncRNAs revealed by ISH suggests their involvement in post-transcriptional gene regulation rather than in epigenetic or transcriptional regulation. Our data provide new insight into testis-associated lncRNAs that will be useful in expression and functional studies of spermatogenesis.

Indexed as

AnimalsComputational BiologyGene Expression ProfilingMaleMiceMice, Inbred StrainsReal-Time Polymerase Chain ReactionRNA, Long NoncodingTestisRNA, Long NoncodingFANTOM5 CAGEIn situ hybridizationLong non-coding RNAMouse spermatogenesis

Identifiers

PMID29411102
OpenAlexW2793387305

What OpenQuestion holds

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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.