Evidence map›Paper›PMID 36344775›Full record

ArticleNature cell biology2022

Intron-encoded cistronic transcripts for minimally invasive monitoring of coding and non-coding RNAs.

Dong-Jiunn Jeffery Truong, Niklas Armbrust, Julian Geilenkeuser, Eva-Maria Lederer, Tobias Heinrich Santl, Maren Beyer, Sebastian Ittermann, Emily Steinmaßl, Mariya Dyka, Gerald Raffl and 6 more

Abstract read
In one paragraph

Article in Nature cell biology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
–field-weighted citation impact
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

5 citing papers in PubMed.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

16 authors.

Dong-Jiunn Jeffery Truong *Institute for Synthetic Biomedicine, Helmholtz Zentrum München, Neuherberg, Germany.ORCID http://orcid.org/0000-0003-1722-8573
Niklas Armbrust *Institute for Synthetic Biomedicine, Helmholtz Zentrum München, Neuherberg, Germany.ORCID http://orcid.org/0000-0002-7396-4949
Julian GeilenkeuserInstitute for Synthetic Biomedicine, Helmholtz Zentrum München, Neuherberg, Germany.ORCID http://orcid.org/0000-0001-5714-7466
Eva-Maria LedererInstitute for Synthetic Biomedicine, Helmholtz Zentrum München, Neuherberg, Germany.ORCID http://orcid.org/0000-0002-1220-1040
Tobias Heinrich SantlInstitute for Synthetic Biomedicine, Helmholtz Zentrum München, Neuherberg, Germany.
Maren BeyerInstitute for Synthetic Biomedicine, Helmholtz Zentrum München, Neuherberg, Germany.
Sebastian IttermannInstitute of Stem Cell Research, Helmholtz Zentrum München, Neuherberg, Germany.
Emily SteinmaßlInstitute for Synthetic Biomedicine, Helmholtz Zentrum München, Neuherberg, Germany.
Mariya DykaInstitute for Synthetic Biomedicine, Helmholtz Zentrum München, Neuherberg, Germany.
Gerald RafflInstitute for Synthetic Biomedicine, Helmholtz Zentrum München, Neuherberg, Germany.ORCID http://orcid.org/0000-0003-0210-0286
Teeradon PhlairaharnInstitute for Synthetic Biomedicine, Helmholtz Zentrum München, Neuherberg, Germany.ORCID http://orcid.org/0000-0001-6031-0578
Tobias GreisleInstitute of Stem Cell Research, Helmholtz Zentrum München, Neuherberg, Germany.ORCID http://orcid.org/0000-0002-3885-4939
Milica ŽivanićInstitute for Synthetic Biomedicine, Helmholtz Zentrum München, Neuherberg, Germany.ORCID http://orcid.org/0000-0002-4967-5709
Markus GroschInstitute of Stem Cell Research, Helmholtz Zentrum München, Neuherberg, Germany.ORCID http://orcid.org/0000-0001-9016-8920
Micha DrukkerInstitute of Stem Cell Research, Helmholtz Zentrum München, Neuherberg, Germany.ORCID http://orcid.org/0000-0002-4279-1125
Gil Gregor WestmeyerInstitute for Synthetic Biomedicine, Helmholtz Zentrum München, Neuherberg, Germany. gil.westmeyer@tum.de.ORCID http://orcid.org/0000-0001-7224-8919

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Despite their fundamental role in assessing (patho)physiological cell states, conventional gene reporters can follow gene expression but leave scars on the proteins or substantially alter the mature messenger RNA. Multi-time-point measurements of non-coding RNAs are currently impossible without modifying their nucleotide sequence, which can alter their native function, half-life and localization. Thus, we developed the intron-encoded scarless programmable extranuclear cistronic transcript (INSPECT) as a minimally invasive transcriptional reporter embedded within an intron of a gene of interest. Post-transcriptional excision of INSPECT results in the mature endogenous RNA without sequence alterations and an additional engineered transcript that leaves the nucleus by hijacking the nuclear export machinery for subsequent translation into a reporter or effector protein. We showcase its use in monitoring interleukin-2 (IL2) after T cell activation and tracking the transcriptional dynamics of the long non-coding RNA (lncRNA) NEAT1 during CRISPR interference-mediated perturbation. INSPECT is a method for monitoring gene transcription without altering the mature lncRNA or messenger RNA of the target of interest.

Indexed as

RNA, Long NoncodingBase SequenceIntronsRNA, MessengerRNA Processing, Post-TranscriptionalRNA, Long NoncodingRNA, Messenger

Identifiers

PMID36344775
PMCPMC9643161

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

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.