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Binding of MAP3773c Protein of Mycobacterium avium subsp. paratuberculosis in the Mouse Ferroportin1 Coding Region
Dulce Liliana Dueñas Mena1, José A Gutiérrez-Pabello2, Kaina Quintero Chávez1
1Facultad de Ciencias Químicas e Ingeniería, Universidad Autónoma de Baja California, Tijuana 22390, Mexico.
Abstract:
Mycobacterium avium subsp. paratuberculosis (MAP) is known to cause paratuberculosis. One notable protein, MAP3773c, plays a critical role in iron metabolism as a transcription factor. This study aims to investigate the binding affinity of MAP3773c to the chromatin of the Ferroportin1 (FPN1) gene in murine macrophage J774 A.1. We conducted a sequence alignment to identify potential interaction sites for MAP3773c. Following this, we used in silico analysis to predict binding interactions, complemented by electrophoretic mobility shift assay (EMSA) to confirm in vitro binding of MAP3773c. The map3773c gene was cloned into the pcDNA3.1 vector, with subsequent expression analysis carried out via Western blotting and real-time PCR. Chromatin immunoprecipitation (CHiP) assays were performed on transfected macrophages to confirm binding in the native chromatin context. Our in silico and in vitro analysis indicated that MAP3773c interacts with two binding motifs within the FPN1 coding region. The ChiP results provided additional validation, demonstrating the binding of MAP3773c to the FPN1 chromatin through successful amplification of the associated chromatin fragment via PCR. Our study demonstrated that MAP3773c binds to FPN1 and provides insight into the role of MAP3773c and its effect on host iron transport.
Insights
Mycobacterium avium paratuberculosis protein MAP3773c binds to the Ferroportin1 (FPN1) gene. This interaction influences host iron transport, offering insights into paratuberculosis pathogenesis.
Area of Science:
- Microbiology
- Molecular Biology
- Host-Pathogen Interactions
Background:
- Mycobacterium avium subsp. paratuberculosis (MAP) causes paratuberculosis.
- MAP3773c is a crucial transcription factor involved in iron metabolism.
- Understanding MAP's interaction with host genes is vital for disease control.
Purpose of the Study:
- To investigate the binding affinity of MAP3773c to the Ferroportin1 (FPN1) gene chromatin.
- To elucidate the role of MAP3773c in regulating host iron transport.
Main Methods:
- Sequence alignment and in silico analysis to predict binding sites.
- Electrophoretic mobility shift assay (EMSA) for in vitro binding confirmation.
- Chromatin immunoprecipitation (CHiP) assays in murine macrophages (J774 A.1).
Main Results:
- MAP3773c was found to interact with two binding motifs in the FPN1 gene.
- In silico and in vitro methods confirmed MAP3773c binding to FPN1.
- CHiP assays validated MAP3773c binding to FPN1 chromatin in a cellular context.
Conclusions:
- MAP3773c directly binds to the FPN1 gene.
- This binding impacts host iron transport mechanisms.
- The study provides novel insights into MAP's virulence factors and host manipulation strategies.
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