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PTDSS1 phosphatidylserine synthase 1 [ Homo sapiens (human) ]

Gene ID: 9791, updated on 28-Oct-2024

Summary

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Official Symbol
PTDSS1provided by HGNC
Official Full Name
phosphatidylserine synthase 1provided by HGNC
Primary source
HGNC:HGNC:9587
See related
Ensembl:ENSG00000156471 MIM:612792; AllianceGenome:HGNC:9587
Gene type
protein coding
RefSeq status
REVIEWED
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
Also known as
LMHD; PSS1; PSSA
Summary
The protein encoded by this gene catalyzes the formation of phosphatidylserine from either phosphatidylcholine or phosphatidylethanolamine. Phosphatidylserine localizes to the mitochondria-associated membrane of the endoplasmic reticulum, where it serves a structural role as well as a signaling role. Defects in this gene are a cause of Lenz-Majewski hyperostotic dwarfism. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Mar 2014]
Expression
Ubiquitous expression in heart (RPKM 35.2), placenta (RPKM 27.0) and 25 other tissues See more
Orthologs
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Genomic context

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See PTDSS1 in Genome Data Viewer
Location:
8q22.1
Exon count:
13
Annotation release Status Assembly Chr Location
RS_2024_08 current GRCh38.p14 (GCF_000001405.40) 8 NC_000008.11 (96261902..96336995)
RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) 8 NC_060932.1 (97387620..97462689)
RS_2024_09 previous assembly GRCh37.p13 (GCF_000001405.25) 8 NC_000008.10 (97274130..97349223)

Chromosome 8 - NC_000008.11Genomic Context describing neighboring genes Neighboring gene ATAC-STARR-seq lymphoblastoid active region 27659 Neighboring gene UQCRB antisense RNA 1 Neighboring gene ubiquinol-cytochrome c reductase binding protein Neighboring gene mitochondrial transcription termination factor 3 Neighboring gene H3K27ac hESC enhancer GRCh37_chr8:97272591-97273284 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 27660 Neighboring gene ReSE screen-validated silencer GRCh37_chr8:97273659-97273983 Neighboring gene H3K27ac hESC enhancer GRCh37_chr8:97273978-97274670 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 27661 Neighboring gene uncharacterized LOC105375652 Neighboring gene Sharpr-MPRA regulatory region 10382 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 27662 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 27663 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 27664 Neighboring gene OCT4-NANOG-H3K4me1 hESC enhancer GRCh37_chr8:97339509-97340044 Neighboring gene OCT4-NANOG-H3K4me1 hESC enhancer GRCh37_chr8:97340045-97340580 Neighboring gene H3K27ac hESC enhancer GRCh37_chr8:97351756-97352256 Neighboring gene uncharacterized LOC102724804 Neighboring gene OCT4-NANOG hESC enhancer GRCh37_chr8:97388962-97389724 Neighboring gene uncharacterized LOC105375653 Neighboring gene RNA, U6 small nuclear 1172, pseudogene

Genomic regions, transcripts, and products

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Go to nucleotide: Graphics FASTA GenBank

Expression

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  • Project title: HPA RNA-seq normal tissues HPA RNA-seq normal tissues
  • Description: RNA-seq was performed of tissue samples from 95 human individuals representing 27 different tissues in order to determine tissue-specificity of all protein-coding genes
  • BioProject: PRJEB4337
  • Publication: PMID 24309898
  • Analysis date: Wed Apr 4 07:08:55 2018

Bibliography

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Related articles in PubMed

  1. A Chinese hamster cDNA encoding a protein essential for phosphatidylserine synthase I activity. Kuge O, et al. J Biol Chem, 1991 Dec 15. PMID 1748687
  2. Disease-related PSS1 mutant impedes the formation and function of osteoclasts. Sugahara S, et al. J Lipid Res, 2023 Nov. PMID 37714410, Free PMC Article
  3. Gain-of-function mutations in the phosphatidylserine synthase 1 (PTDSS1) gene cause Lenz-Majewski syndrome. Sousa SB, et al. Nat Genet, 2014 Jan. PMID 24241535
  4. Lenz-Majewski mutations in PTDSS1 affect phosphatidylinositol 4-phosphate metabolism at ER-PM and ER-Golgi junctions. Sohn M, et al. Proc Natl Acad Sci U S A, 2016 Apr 19. PMID 27044099, Free PMC Article
  5. Cutis laxa and excessive bone growth due to de novo mutations in PTDSS1. Piard J, et al. Am J Med Genet A, 2018 Mar. PMID 29341480, Free PMC Article

See all (80) citations in PubMed

GeneRIFs: Gene References Into Functions

What's a GeneRIF?
  1. Disease-related PSS1 mutant impedes the formation and function of osteoclasts.
    Title: Disease-related PSS1 mutant impedes the formation and function of osteoclasts.
  2. Topology of phosphatidylserine synthase 1 in the endoplasmic reticulum membrane.
    Title: Topology of phosphatidylserine synthase 1 in the endoplasmic reticulum membrane.
  3. used transpose-mediated transgenesis to attempt to stably express wild-type and mutant forms of human PTDSS1 ubiquitously or specifically in chondrocytes, osteoblasts or osteoclasts in zebrafish
    Title: Analysis of transgenic zebrafish expressing the Lenz-Majewski syndrome gene PTDSS1 in skeletal cell lineages.
  4. we report here three patients with LMS and heterozygous mutations in PTDSS1. We describe an adult phenotype and two novel PTDSS1 mutations. We suggest that LMS should be considered in the differential diagnosis of a newborn with CL.
    Title: Cutis laxa and excessive bone growth due to de novo mutations in PTDSS1.
  5. RYR2, PTDSS1 and AREG are autism susceptibility genes that are implicated in a Lebanese population-based study of copy number variations in this disease.
    Title: RYR2, PTDSS1 and AREG genes are implicated in a Lebanese population-based study of copy number variation in autism.
  6. PSS1 mutations not only affect cellular PS levels and distribution but also lead to a more complex imbalance in lipid homeostasis by disturbing PI4P metabolism.
    Title: Lenz-Majewski mutations in PTDSS1 affect phosphatidylinositol 4-phosphate metabolism at ER-PM and ER-Golgi junctions.
  7. Gain-of-function missense mutations in the phosphatidylserine synthase 1 (PTDSS1) gene cause Lenz-Majewski syndrome.
    Title: Gain-of-function mutations in the phosphatidylserine synthase 1 (PTDSS1) gene cause Lenz-Majewski syndrome.
  8. Clinical trial of gene-disease association and gene-environment interaction. (HuGE Navigator)
    Title: Personalized smoking cessation: interactions between nicotine dose, dependence and quit-success genotype score.
  9. Purification and characterization of human phosphatidylserine synthases 1 and 2.
    Title: Purification and characterization of human phosphatidylserine synthases 1 and 2.
Submit: New GeneRIF Correction

Phenotypes

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Find tests for this gene in the NIH Genetic Testing Registry (GTR)

Review eQTL and phenotype association data in this region using PheGenI

Associated conditions

Description Tests
Lenz-Majewski hyperostosis syndrome
MedGen: C0432269 OMIM: 151050 GeneReviews: Not available
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EBI GWAS Catalog

Description
Novel genetic loci identified for the pathophysiology of childhood obesity in the Hispanic population.
EBI GWAS Catalog

Variation

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See variants in ClinVar

See studies and variants in dbVar

See Variation Viewer (GRCh37.p13)

See Variation Viewer (GRCh38)

Genotypes

HIV-1 interactions

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Replication interactions

Interaction Pubs
Knockdown of phosphatidylserine synthase 1 (PTDSS1) by siRNA inhibits the early stages of HIV-1 replication in 293T cells infected with VSV-G pseudotyped HIV-1 PubMed

Protein interactions

Protein Gene Interaction Pubs
Envelope surface glycoprotein gp120 env Tandem affinity purification and mass spectrometry analysis identify phosphatidylserine synthase 1 (PTDSS1), HIV-1 Gag, Gag/Pol, gp120, and Nef incorporated into staufen1 RNP complexes isolated from HIV-1-expressing cells PubMed
Gag-Pol gag-pol Tandem affinity purification and mass spectrometry analysis identify phosphatidylserine synthase 1 (PTDSS1), HIV-1 Gag, Gag/Pol, gp120, and Nef incorporated into staufen1 RNP complexes isolated from HIV-1-expressing cells PubMed
Nef nef Tandem affinity purification and mass spectrometry analysis identify phosphatidylserine synthase 1 (PTDSS1), HIV-1 Gag, Gag/Pol, gp120, and Nef incorporated into staufen1 RNP complexes isolated from HIV-1-expressing cells PubMed
Pr55(Gag) gag Tandem affinity purification and mass spectrometry analysis identify phosphatidylserine synthase 1 (PTDSS1), HIV-1 Gag, Gag/Pol, gp120, and Nef incorporated into staufen1 RNP complexes isolated from HIV-1-expressing cells PubMed

Go to the HIV-1, Human Interaction Database

Pathways from PubChem

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Interactions

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Products Interactant Other Gene Complex Source Pubs Description

General gene information

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Markers

Homology

Clone Names

  • KIAA0024

Gene Ontology Provided by GOA

Function Evidence Code Pubs
enables L-serine-phosphatidylcholine phosphatidyltransferase activity IDA
Inferred from Direct Assay
more info
 PubMed 
enables L-serine-phosphatidylcholine phosphatidyltransferase activity IMP
Inferred from Mutant Phenotype
more info
 PubMed 
enables L-serine-phosphatidylethanolamine phosphatidyltransferase activity IDA
Inferred from Direct Assay
more info
 PubMed 
enables L-serine-phosphatidylethanolamine phosphatidyltransferase activity IMP
Inferred from Mutant Phenotype
more info
 PubMed 
enables transferase activity TAS
Traceable Author Statement
more info
  
Process Evidence Code Pubs
involved_in phosphatidylserine biosynthetic process IDA
Inferred from Direct Assay
more info
 PubMed 
involved_in phosphatidylserine biosynthetic process IEA
Inferred from Electronic Annotation
more info
  
involved_in phosphatidylserine biosynthetic process TAS
Traceable Author Statement
more info
  
Component Evidence Code Pubs
located_in endoplasmic reticulum membrane ISS
Inferred from Sequence or Structural Similarity
more info
  
located_in endoplasmic reticulum membrane TAS
Traceable Author Statement
more info
  
located_in membrane HDA PubMed 
located_in membrane ISS
Inferred from Sequence or Structural Similarity
more info
  

General protein information

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Preferred Names
phosphatidylserine synthase 1
Names
PSS-1
ptdSer synthase 1
serine-exchange enzyme I
NP_001277154.1
NP_055569.1

NCBI Reference Sequences (RefSeq)

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RefSeqs maintained independently of Annotated Genomes

These reference sequences exist independently of genome builds. Explain

These reference sequences are curated independently of the genome annotation cycle, so their versions may not match the RefSeq versions in the current genome build. Identify version mismatches by comparing the version of the RefSeq in this section to the one reported in Genomic regions, transcripts, and products above.

Genomic

  1. NG_034054.2 RefSeqGene

    Range
    5002..80095
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

mRNA and Protein(s)

  1. NM_001290225.2 → NP_001277154.1  phosphatidylserine synthase 1 isoform 2

    See identical proteins and their annotated locations for NP_001277154.1

    Status: REVIEWED

    Description
    Transcript Variant: This variant (2) lacks two consecutive alternate exons compared to variant 1. The resulting isoform (2) is shorter at the N-terminus compared to isoform 1.
    Source sequence(s)
    AP003465, BC002376, BM459031, HY087183
    UniProtKB/TrEMBL
    Q9BSY0
    Conserved Domains (1) summary
    pfam03034
    Location:1 → 225
    PSS; Phosphatidyl serine synthase

  2. NM_014754.3 → NP_055569.1  phosphatidylserine synthase 1 isoform 1

    See identical proteins and their annotated locations for NP_055569.1

    Status: REVIEWED

    Description
    Transcript Variant: This variant (1) represents the longer transcript and encodes the longer isoform (1).
    Source sequence(s)
    AP003465, BC004192, BM459031, HY087183
    Consensus CDS
    CCDS6271.1
    UniProtKB/Swiss-Prot
    B4DE85, E5RFC5, P48651, Q9BUQ5
    UniProtKB/TrEMBL
    A8KAH1
    Related
    ENSP00000430548.1, ENST00000517309.6
    Conserved Domains (1) summary
    pfam03034
    Location:96 → 371
    PSS; Phosphatidyl serine synthase

RefSeqs of Annotated Genomes: GCF_000001405.40-RS_2024_08

The following sections contain reference sequences that belong to a specific genome build. Explain

Reference GRCh38.p14 Primary Assembly

Genomic

  1. NC_000008.11 Reference GRCh38.p14 Primary Assembly

    Range
    96261902..96336995
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060932.1 Alternate T2T-CHM13v2.0

    Range
    97387620..97462689
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
Nucleotide Protein
Heading Accession and Version
Protein Accession Links
GenPept Link UniProtKB Link
P48651.1 GenPept UniProtKB/Swiss-Prot:P48651

Gene LinkOut

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