Evidence map›Paper›PMID 35409004›Full record

ArticleInternational journal of molecular sciences2022

Characteristics of Transfer RNA-Derived Fragments Expressed during Human Renal Cell Development: The Role of Dicer in tRF Biogenesis.

Marek Kazimierczyk, Marta Wojnicka, Ewa Biała, Paulina Żydowicz-Machtel, Barbara Imiołczyk, Tomasz Ostrowski, Anna Kurzyńska-Kokorniak, Jan Wrzesinski

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed, 1 pooled it
8.1field-weighted citation impact, top 1% 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, 1 synthesis or guideline pooled it, 44 citations in OpenAlex.

  1. Pooled it
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  6. Roles and regulation of tRNA-derived small RNAs in animals.Nature reviews. Molecular cell biology · 2024
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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

8 authors at 1 institution in 1 country.

Marek KazimierczykInstitute of Bioorganic Chemistry, Polish Academy of Sciences, 61-704 Poznań, Poland.
Marta WojnickaInstitute of Bioorganic Chemistry, Polish Academy of Sciences, 61-704 Poznań, Poland.
Ewa BiałaInstitute of Bioorganic Chemistry, Polish Academy of Sciences, 61-704 Poznań, Poland.
Paulina Żydowicz-MachtelInstitute of Bioorganic Chemistry, Polish Academy of Sciences, 61-704 Poznań, Poland.
Barbara ImiołczykInstitute of Bioorganic Chemistry, Polish Academy of Sciences, 61-704 Poznań, Poland.
Tomasz OstrowskiInstitute of Bioorganic Chemistry, Polish Academy of Sciences, 61-704 Poznań, Poland.
Anna Kurzyńska-KokorniakInstitute of Bioorganic Chemistry, Polish Academy of Sciences, 61-704 Poznań, Poland.ORCID 0000-0002-7034-3370
Jan WrzesinskiInstitute of Bioorganic Chemistry, Polish Academy of Sciences, 61-704 Poznań, Poland.ORCID 0000-0002-3777-4320
Institute of Bioorganic Chemistry, Polish Academy of Sciences · PL

Funding

Polish Academy of Sciences 2016/21/NZ2/03468 to J.W. and 2016/22/E/NZ1/00422 to A.K-K
6 · The paper itself

Abstract

tRNA-derived fragments participate in the regulation of many processes, such as gene silencing, splicing and translation in many organisms, ranging from bacteria to humans. We were interested to know how tRF abundance changes during the different stages of renal cell development. The research model used here consisted of the following human renal cells: hESCs, HEK-293T, HK-2 and A-489 kidney tumor cells, which, together, mimic the different stages of kidney development. The characteristics of the most abundant tRFs, tRFGly(CCC), tRFVal(AAC) and tRFArg(CCU), were presented. It was found that these parental tRNAs present in cells are the source of many tRFs, thus increasing the pool of potential regulatory RNAs. Indeed, a bioinformatic analysis showed the possibility that tRFGly(CCC) and tRRFVal(AAC) could regulate the activity of a range of kidney proteins. Moreover, the distribution of tRFs and the efficiency of their expression is similar in adult and embryonic stem cells. During the formation of tRFs, HK-2 cells resemble A-498 cancer cells more than other cells. Additionally, we postulate the involvement of Dicer nuclease in the formation of tRF-5b in all the analyzed tRNAs. To confirm this, 293T NoDice cells, which in the absence of Dicer activity do not generate tRF-5b, were used.

Indexed as

Computational BiologyRNA, TransferAdultHumansKidneyRNA, TransferDicerNorthern blotrenal cellstRFtRNA-derived fragment

Identifiers

PMID35409004
PMCPMC8998818
OpenAlexW4220999986

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.