Evidence map›Paper›PMID 42703972›Full record

ArticleNucleic acids research2026

Primer- and template-independent RNA polymerization by terminal nucleotidyltransferase TENT4B.

Neha Nagpal, Albert K Tai, Yick W Fong, Suneet Agarwal

Abstract read
In one paragraph

Article in Nucleic acids research, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

What it found

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2 · The registry

The trial behind it

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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

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

4 authors.

Neha NagpalDivision of Hematology/Oncology and Stem Cell Program, Boston Children's Hospital, Boston, MA 02115, United States.
Albert K TaiDepartment of Immunology, Tufts University School of Medicine, Boston, MA, United States.
Yick W FongHarvard Stem Cell Institute, Cambridge, MA, United States.ORCID 0000-0002-8498-7169
Suneet AgarwalDivision of Hematology/Oncology and Stem Cell Program, Boston Children's Hospital, Boston, MA 02115, United States.ORCID 0000-0003-4910-3118

Funding

Regulation of the telomerase RNA component in hematopoiesisR01DK107716 · NIDDK · BOSTON CHILDREN'S HOSPITAL · PI SUNEET AGARWAL · 2016 to 2026
$5.0M
Overcoming epigenetic barriers to somatic cell reprogramming by the XPC DNA repair complexR01GM152463 · NIGMS · BRIGHAM AND WOMEN'S HOSPITAL · PI FONG, YICK WAH · 2024 to 2025
$716k
Boston Children's HospitalNIDDK NIH HHS R01 DK107716NIDDK NIH HHS R01DK107716NIGMS NIH HHS R01 GM152463NIGMS NIH HHS R01GM152463Team TelomereUplifting Athletes Young Investigator Draft
6 · The paper itself

Abstract

RNA synthesis by eukaryotic polymerases requires existing polynucleotides to serve as templates or primers. Here, we describe primer- and template-free RNA generation by human terminal nucleotidyltransferase 4B (TENT4B) via de novo polymerization of free nucleotides. We observed that recombinant TENT4B (rTENT4B) consumes ATP to yield inorganic pyrophosphate in the absence of a primer or template, concurrent with the appearance of oligomeric poly-adenosine RNA products. Remarkably, 5' labels on γ-phosphate-modified ATP or GTP are retained during polymerization in the presence of unlabeled nucleotide triphosphates (NTPs). These polymers are created at a similar efficiency irrespective of the inclusion of a primer, indicating robust RNA synthesis by rTENT4B from free NTPs. While canonical purine NTPs are favored, nucleotide diphosphates (NDPs) can also serve as substrates for rTENT4B-mediated de novo RNA polymerization. rTENT4B-mediated RNA synthesis using free adenosine nucleotides shows high processivity to generate 1000s-mers, whereas guanosine nucleotide polymerization is strongly and uniformly self-limited and yields a 3'-exonuclease-resistant oligonucleotide. Interrogation of other RNA polymerases reveals potential capacity for de novo polymerization using free ATP, albeit at significantly higher substrate concentrations and lower efficiency compared with rTENT4B. Our data provide definitive evidence of efficient template-free de novo RNA synthesis by a eukaryotic polymerase.

Indexed as

NucleotidyltransferasesRNAAdenosine TriphosphateHumansPolymerizationTemplates, GeneticAdenosine TriphosphateNucleotidyltransferasesRNARNA primers

Identifiers

PMID42703972
PMCPMC13548058

What OpenQuestion holds

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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.