Evidence map›Paper›PMID 20660478›Full record

ArticleNucleic acids research2010

Synthesis and biological activity of artificial mRNA prepared with novel phosphorylating reagents.

Seigo Nagata, Tomohiro Hamasaki, Koichi Uetake, Hirofumi Masuda, Kazuchika Takagaki, Natsuhisa Oka, Takeshi Wada, Tadaaki Ohgi, Junichi Yano

Open access · goldAbstract read
In one paragraph

Article in Nucleic acids research, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
0.8field-weighted citation impact, top 28% 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

14 citing papers in PubMed, 37 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Article
  6. Review
  7. Review
  8. Covalent labeling of nucleic acids.Chemical Society reviews · 2020
    Review
  9. Review
  10. ADP heptose, a novel pathogen-associated molecular pattern identified inFASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2019
    Article
  11. Chemical synthesis of long RNAs with terminal 5'-phosphate groups.Chemistry (Weinheim an der Bergstrasse, Germany) · 2017
    Article
  12. Synthetic mRNA capping.Beilstein journal of organic chemistry · 2017
    Review
  13. Article
  14. 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 2 institutions in 1 country.

Seigo NagataDiscovery Research Laboratories, Nippon Shinyaku Co, Ltd, 3-14-1 Sakura, Tsukuba, Ibaraki 305-0003, Japan. s.nagata@po.nippon-shinyaku.co.jp
Tomohiro Hamasaki
Koichi Uetake
Hirofumi Masuda
Kazuchika Takagaki
Natsuhisa Oka
Takeshi Wada
Tadaaki Ohgi
Junichi Yano
The University of Tokyo · JPNippon Shinyaku (Japan) · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Though medicines that target mRNA are under active investigation, there has been little or no effort to develop mRNA itself as a medicine. Here, we report the synthesis of a 130-nt mRNA sequence encoding a 33-amino-acid peptide that includes the sequence of glucagon-like peptide-1, a peptide that stimulates glucose-dependent insulin secretion from the pancreas. The synthesis method used, which had previously been developed in our laboratory, was based on the use of 2-cyanoethoxymethyl as the 2'-hydroxy protecting group. We also developed novel, highly reactive phosphotriester pyrophosphorylating reagents to pyrophosphorylate the 5'-end of the 130-mer RNA in preparation for capping. We completed the synthesis of the artificial mRNA by the enzymatic addition of a 5'-cap and a 3'-poly(A) tail to the pyrophosphorylated 130-mer and showed that the resulting mRNA supported protein synthesis in a cell-free system and in whole cells. As far as we know, this is the first time that mRNA has been prepared from a chemically synthesized RNA sequence. As well as providing a research tool for the intracellular expression of peptides, the technology described here may be used for the production of mRNA for medical applications.

Indexed as

3' Untranslated RegionsAnimalsCHO CellsCricetinaeCricetulusGlucagon-Like Peptide 1Indicators and ReagentsMethyltransferasesPhosphorylationPoly ARNA CapsRNA, Messenger3' Untranslated RegionsGlucagon-Like Peptide 1Indicators and ReagentsMethyltransferasesmRNA (nucleoside-O(2'))-methyltransferasePoly ARNA CapsRNA, Messenger

Identifiers

PMID20660478
PMCPMC2995060
OpenAlexW2082725317

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.