Evidence map›Paper›PMID 34136101›Full record

ArticleComputational and structural biotechnology journal2021

Modelling of SHMT1 riboregulation predicts dynamic changes of serine and glycine levels across cellular compartments.

Michele Monti, Giulia Guiducci, Alessio Paone, Serena Rinaldo, Giorgio Giardina, Francesca Romana Liberati, Francesca Cutruzzolá, Gian Gaetano Tartaglia

Open access · goldAbstract read
In one paragraph

Article in Computational and structural biotechnology journal, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
1.1field-weighted citation impact, top 23% 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

15 citing papers in PubMed, 17 citations in OpenAlex.

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  5. RNA-binding proteins as versatile metabolic regulators.npj metabolic health and disease · 2025
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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 3 institutions in 2 countries.

Michele MontiCentre for Genomic Regulation (CRG), The Barcelona Institute for Science and Technology, Dr. Aiguader 88, 08003 Barcelona, Spain.
Giulia GuiducciDepartment of Biochemical Sciences "A.Rossi Fanelli", Sapienza University of Rome, P-le A.Moro 5, 00185 Rome, Italy.
Alessio PaoneDepartment of Biochemical Sciences "A.Rossi Fanelli", Sapienza University of Rome, P-le A.Moro 5, 00185 Rome, Italy.
Serena RinaldoDepartment of Biochemical Sciences "A.Rossi Fanelli", Sapienza University of Rome, P-le A.Moro 5, 00185 Rome, Italy.
Giorgio GiardinaDepartment of Biochemical Sciences "A.Rossi Fanelli", Sapienza University of Rome, P-le A.Moro 5, 00185 Rome, Italy.
Francesca Romana LiberatiDepartment of Biochemical Sciences "A.Rossi Fanelli", Sapienza University of Rome, P-le A.Moro 5, 00185 Rome, Italy.
Francesca CutruzzoláDepartment of Biochemical Sciences "A.Rossi Fanelli", Sapienza University of Rome, P-le A.Moro 5, 00185 Rome, Italy.
Gian Gaetano TartagliaCentre for Genomic Regulation (CRG), The Barcelona Institute for Science and Technology, Dr. Aiguader 88, 08003 Barcelona, Spain.
Sapienza University of Rome · ITInstitució Catalana de Recerca i Estudis Avançats · ESItalian Institute of Technology · IT

Funding

Wellcome Trust
6 · The paper itself

Abstract

Human serine hydroxymethyltransferase (SHMT) regulates the serine-glycine one carbon metabolism and plays a role in cancer metabolic reprogramming. Two SHMT isozymes are acting in the cell: SHMT1 encoding the cytoplasmic isozyme, and SHMT2 encoding the mitochondrial one. Here we present a molecular model built on experimental data reporting the interaction between SHMT1 protein and SHMT2 mRNA, recently discovered in lung cancer cells. Using a stochastic dynamic model, we show that RNA moieties dynamically regulate serine and glycine concentration, shaping the system behaviour. For the first time we observe an active functional role of the RNA in the regulation of the serine-glycine metabolism and availability, which unravels a complex layer of regulation that cancer cells exploit to fine tune amino acids availability according to their metabolic needs. The quantitative model, complemented by an experimental validation in the lung adenocarcinoma cell line H1299, exploits RNA molecules as metabolic switches of the SHMT1 activity. Our results pave the way for the development of RNA-based molecules able to unbalance serine metabolism in cancer cells.

Indexed as

Metabolic networksRNA-binding proteinRNA-protein interactionsSerine/Glycine metabolism

Identifiers

PMID34136101
PMCPMC8175283
OpenAlexW3162078601

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.