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Cited by 9Trypanosoma species research and implicationsResearch on Leishmaniasis StudiesVector-borne infectious diseases

The DOI matches its Crossref record; 61 of the 61 references it cites were found in a registry or an index.

The Elusive Trypanosoma cruzi Disperse Gene Protein Family (DGF-1)

Open access
Ramírez, José Luis·2023·Pathogens

Published version of a preprint

Abstract

Chagas disease, caused by Trypanosoma cruzi infections, is included in the group of neglected diseases, and efforts to develop new therapeutic or immunoprevention approaches have not been successful. After the publication of the T. cruzi genome, the number of molecular and biochemical studies on this parasite has increased considerably, many of which are focused on families of variant surface proteins, especially trans-sialidases, mucins, and mucin-associated proteins. The disperse gene protein 1 family (DGF-1) is one of the most abundant families in the T. cruzi genome; however, the large gene size, high copy numbers, and low antibody titers detected in infected humans make it an unattractive study target. However, here we argue that given the ubiquitous presence in all T. cruzi species, and physicochemical characteristics, the DGF-1 gene family may play and important role in host-parasite interactions.

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Crossref · 10.3390/pathogens12020292

Cites

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Figures

Figure 1 Schematic representation of T. cruzi’s DGF-1.2 protein in the cell membrane. Cell membrane cytoplasmic-extracellular topology predicted by UNIPRO. Numbers mark domains predicted by different structure-prediction software. 1. β-sheet structure (aa 60–140) identity to Human Galectin 7 2–3 (SWISSPRO); pectin-lyase superfamily IPRO11050 (aa 882–987) (InterPro); Regions 2, 3, and 4 with several structural predictions based on sequence identity, structure similarity, and amino acid folding: Complement component C9 receptor (aa 1189–1227) (aa 1584–1622) (SWISS-PRO); Notch ligand (Panther prediction) (aa 1192–1621); pectine lyase-fold (aa 1670–1898) (Alphafold-InterPro); arabinofuranosyltransferase aftd2 from mycobacteria (aa1993–2170) structure prediction confidence 96% (Phyre-2); 4. Threonine-rich region (aa 2800–2927) PROSITE, and structure of tailspike protein gp49 from pseudomonas phage2 lka1 88% confidence (Phyre-2), epitopes from reference [21] are located in this region; 5. Transmembrane helices region DGF1_14, DGF_1.5 (InterPro). Blue cylinders: Transmembrane domains. Graph made with BioRender.
Figure 1 Schematic representation of T. cruzi’s DGF-1.2 protein in the cell membrane. Cell membrane cytoplasmic-extracellular topology predicted by UNIPRO. Numbers mark domains predicted by different structure-prediction software. 1. β-sheet structure (aa 60–140) identity to Human Galectin 7 2–3 (SWISSPRO); pectin-lyase superfamily IPRO11050 (aa 882–987) (InterPro); Regions 2, 3, and 4 with several structural predictions based on sequence identity, structure similarity, and amino acid folding: Complement component C9 receptor (aa 1189–1227) (aa 1584–1622) (SWISS-PRO); Notch ligand (Panther prediction) (aa 1192–1621); pectine lyase-fold (aa 1670–1898) (Alphafold-InterPro); arabinofuranosyltransferase aftd2 from mycobacteria (aa1993–2170) structure prediction confidence 96% (Phyre-2); 4. Threonine-rich region (aa 2800–2927) PROSITE, and structure of tailspike protein gp49 from pseudomonas phage2 lka1 88% confidence (Phyre-2), epitopes from reference [21] are located in this region; 5. Transmembrane helices region DGF1_14, DGF_1.5 (InterPro). Blue cylinders: Transmembrane domains. Graph made with BioRender.CC BY · PubMed Central
Figure 2 Schematic representation of T. cruzi DGF-1.2 protein and Bodo saltans Bonodin gene [17]. Barrels represent transmembrane regions; SP, signal peptide; N and C protein terminals; I, intracellular regions; E, extracellular regions. Graph made with BioRender.
Figure 2 Schematic representation of T. cruzi DGF-1.2 protein and Bodo saltans Bonodin gene [17]. Barrels represent transmembrane regions; SP, signal peptide; N and C protein terminals; I, intracellular regions; E, extracellular regions. Graph made with BioRender.CC BY · PubMed Central

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Citations

Cites

Show all 61 references

Research works printed but not linked: 1

  1. Olivares, 2000, Genome clustering of the Trypanosoma cruzi non-long terminal L1Tc retrotransposon with defined intersperse repeated DNA elements, Electrophoresis, 21, 2973, 10.1002/1522-2683(20000801)21:14<2973::AID-ELPS2973>3.0.CO;2-4 · doi:10.1002/1522-2683(20000801)21:14<2973::aid-elps2973>3.0.co;2-4

Metadata

Authors
Ramírez, J. L.
Affiliations
Instituto de Estudios Avanzados, Caracas, Venezuela and Universidad Central de Venezuela, Caracas 1080, Venezuela
Venue
Pathogens
Publisher
MDPI AG
Published
2023-02-10
Volume
12
Issue
2
Pages
292
ISSN
2076-0817 (ISSN-L)
OpenAlex
W4319985730
Cited by
9
References
61
Citations by year
2026: 4 · 2025: 4 · 2023: 1
FWCI
0.35
Type
journal article
Language
en
Open access
Locations
  • Pathogens (publishedVersion, cc-by)
  • Preprints.org (acceptedVersion, cc-by)
  • PubMed Central (publishedVersion, cc-by)
  • PubMed (publishedVersion)
  • DOAJ (DOAJ: Directory of Open Access Journals) (submittedVersion, cc-by-sa)
Funders
FONACYT-Mincyt Venezuela (018-2022)
Topics
  • Health Sciences › Medicine › Epidemiology › Trypanosoma species research and implications
  • Health Sciences › Medicine › Public Health, Environmental and Occupational Health › Research on Leishmaniasis Studies
  • Life Sciences › Immunology and Microbiology › Parasitology › Vector-borne infectious diseases
Keywords
Trypanosoma cruzi, Chagas disease, host-parasite interactions, variant surface proteins, trans-sialidase, mucin, antibody titers, neglected diseases

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CoChat. (2026). Citation check: The Elusive Trypanosoma cruzi Disperse Gene Protein Family (DGF-1). https://app.cochat.ai/papers/10.3390/pathogens12020292
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Ramírez, J. L. (2023). The Elusive Trypanosoma cruzi Disperse Gene Protein Family (DGF-1). Pathogens. https://doi.org/10.3390/pathogens12020292

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