Evidence map›Paper›PMID 33662400›Full record

ArticleThe Journal of biological chemistry

SSSPTA is essential for serine palmitoyltransferase function during development and hematopoiesis.

Velayoudame Parthibane, Jing Lin, Diwash Acharya, Thiruvaimozhi Abimannan, Sargur Madabushi Srideshikan, Kimberly Klarmann, Acong Yang, Ferri Soheilian, Kunio Nagashima, Stephen D Fox and 5 more

Open access · goldAbstract read
In one paragraph

Article in The Journal of biological chemistry. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
1.1field-weighted citation impact, top 24% 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

12 citing papers in PubMed, 16 citations in OpenAlex.

  1. Review
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  4. Article
  5. Review
  6. Article
  7. Article
  8. Article
  9. Review
  10. Drug Development in the Field of Sphinogolipid Metabolism.Advances in experimental medicine and biology · 2022
    Article
  11. Review
  12. 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

15 authors at 1 institution in 1 country.

Velayoudame ParthibaneCancer and Developmental Biology Laboratory, National Cancer Institute, Frederick, Maryland, USA.
Jing LinCancer and Developmental Biology Laboratory, National Cancer Institute, Frederick, Maryland, USA.
Diwash AcharyaCancer and Developmental Biology Laboratory, National Cancer Institute, Frederick, Maryland, USA.
Thiruvaimozhi AbimannanCancer and Developmental Biology Laboratory, National Cancer Institute, Frederick, Maryland, USA.
Sargur Madabushi SrideshikanCancer and Developmental Biology Laboratory, National Cancer Institute, Frederick, Maryland, USA.
Kimberly KlarmannMouse Cancer Genetics Program, National Cancer Institute, Frederick, Maryland, USA.
Acong YangRNA Biology Laboratory, Center for Cancer Research, National Cancer Institute, Frederick, Maryland, USA.
Ferri SoheilianElectron Microscopy Group, Center for Cancer Research, National Cancer Institute, Frederick, Maryland, USA.
Kunio NagashimaElectron Microscopy Group, Center for Cancer Research, National Cancer Institute, Frederick, Maryland, USA.
Stephen D FoxMass Spectrometry Group, Center for Cancer Research, National Cancer Institute, Frederick, Maryland, USA.
Thorkell AndressonMass Spectrometry Group, Center for Cancer Research, National Cancer Institute, Frederick, Maryland, USA.
Lino TessarolloMouse Cancer Genetics Program, National Cancer Institute, Frederick, Maryland, USA.
Jonathan R KellerMouse Cancer Genetics Program, National Cancer Institute, Frederick, Maryland, USA.
Usha AcharyaCancer and Developmental Biology Laboratory, National Cancer Institute, Frederick, Maryland, USA. Electronic address: acharyaur@nih.gov.
Jairaj K AcharyaCancer and Developmental Biology Laboratory, National Cancer Institute, Frederick, Maryland, USA. Electronic address: acharyaj@mail.nih.gov.
National Cancer Institute · US

Funding

Molecular-Cellular Regulation of Hematopoietic Stem CellsZIABC010001 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI KELLER, JONATHAN R · 2009 to 2024
$16.8M
Sphingolipid Signaling in MammalsZIABC011187 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI ACHARYA, JAIRAJ · 2009 to 2025
$15.9M
Gene Targeting FacilityZICBC011265 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI TESSAROLLO, LINO · 2010 to 2025
$8.9M
6 · The paper itself

Abstract

Serine palmitoyltransferase complex (SPT) mediates the first and rate-limiting step in the de novo sphingolipid biosynthetic pathway. The larger subunits SPTLC1 and SPTLC2/SPTLC3 together form the catalytic core while a smaller third subunit either SSSPTA or SSSPTB has been shown to increase the catalytic efficiency and provide substrate specificity for the fatty acyl-CoA substrates. The in vivo biological significance of these smaller subunits in mammals is still unknown. Here, using two null mutants, a conditional null for ssSPTa and a null mutant for ssSPTb, we show that SSSPTA is essential for embryogenesis and mediates much of the known functions of the SPT complex in mammalian hematopoiesis. The ssSPTa null mutants are embryonic lethal at E6.5 much like the Sptlc1 and Sptlc2 null alleles. Mx1-Cre induced deletion of ssSPTa leads to lethality and myelopoietic defect. Chimeric and competitive bone marrow transplantation experiments show that the defect in myelopoiesis is accompanied by an expansion of the Lin

Indexed as

Acyl Coenzyme AAnimalsBone Marrow CellsCatalytic DomainCell DifferentiationHematopoiesisMiceMice, Inbred C57BLMice, KnockoutSerine C-PalmitoyltransferaseSphingolipidsSubstrate SpecificityAcyl Coenzyme ASerine C-PalmitoyltransferaseSphingolipidsssSPTabone marrow cellsER stressgranulopoiesishematopoiesishematopoietic stem cellsmyelopoiesisserine palmitoyltransferasesphingolipidssSPTassSPTb

Identifiers

PMID33662400
PMCPMC8047174
OpenAlexW3134817790

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.