Evidence map›Paper›PMID 12138190›Full record

ArticleMolecular and cellular biology2002

A functional screen for Myc-responsive genes reveals serine hydroxymethyltransferase, a major source of the one-carbon unit for cell metabolism.

Mikhail A Nikiforov, Sanjay Chandriani, Brenda O'Connell, Oleksi Petrenko, Iulia Kotenko, Andrew Beavis, John M Sedivy, Michael D Cole

Open access · greenAbstract read
In one paragraph

Article in Molecular and cellular biology, 2002. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 135 papers.

0numbers the graph read from it
0cells of the map it votes in
135citing papers in PubMed
2.1field-weighted citation impact, top 13% 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

135 citing papers in PubMed, 200 citations in OpenAlex.

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75 more citing papers are in PubMed but not listed here.

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 2 institutions in 1 country.

Mikhail A NikiforovDepartment of Molecular Biology, Princeton University, Princeton, New Jersey 08544, USA.
Sanjay Chandriani
Brenda O'Connell
Oleksi Petrenko
Iulia Kotenko
Andrew Beavis
John M Sedivy
Michael D Cole
Princeton University · USBrown University · US

Funding

FUNCTION OF THE C-MYC ONCOGENER01CA055248 · NCI · PRINCETON UNIVERSITY · PI COLE, MICHAEL DAVID · 1992 to 2020
$8.6M
NCI NIH HHS R01 CA055248
6 · The paper itself

Abstract

A cDNA library enriched with Myc-responsive cDNAs but depleted of myc cDNAs was used in a functional screen for growth enhancement in c-myc-null cells. A cDNA clone for mitochondrial serine hydroxymethyltransferase (mSHMT) that was capable of partial complementation of the growth defects of c-myc-null cells was identified. Expression analysis and chromatin immunoprecipitation demonstrated that mSHMT is a direct Myc target gene. Furthermore, a separate gene encoding the cytoplasmic isoform of the same enzyme is also a direct target of Myc regulation. SHMT enzymes are the major source of the one-carbon unit required for folate metabolism and for the biosynthesis of nucleotides and amino acids. Our data establish a novel functional link between Myc and the regulation of cellular metabolism.

Indexed as

Cell Physiological PhenomenaAnimalsCarbonCells, CulturedCell SeparationFibroblastsFlow CytometryGene LibraryGenes, mycGlycine HydroxymethyltransferaseHumansMitochondriaPromoter Regions, GeneticProto-Oncogene Proteins c-mycRatsRats, Mutant StrainsCarbonGlycine HydroxymethyltransferaseProto-Oncogene Proteins c-myc

Identifiers

PMID12138190
PMCPMC133987
OpenAlexW2141732292

What OpenQuestion holds

Textmetadata
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.