Analysis of new lactotransferrin gene variants in a case-control study related to periodontal disease in dog.

Mol Biol Rep

IBB/CGB-UTAD (Institute for Biotechnology and Bioengineering, Centre of Genomics and Biotechnology, University of Trás-os-Montes e Alto Douro), Quinta de Prados, P.O. Box 1013, 5001-801, Vila Real, Portugal.

Published: April 2012

The molecular and genetic research has contributed to a better understanding of the periodontal disease (PD) in humans and has shown that many genes play a role in the predisposition and progression of this complex disease. Variations in human lactotransferrin (LTF) gene appear to affect anti-microbial functions of this molecule, influencing the PD susceptibility. PD is also a major health problem in small animal practice, being the most common inflammatory disease found in dogs. Nevertheless, the research in genetic predisposition to PD is an unexplored subject in this species. This work aims to contribute to the characterization of the genetic basis of canine PD. In order to identify genetic variations and verify its association with PD, was performed a molecular analysis of LTF gene in a case-control approach, including 40 dogs in the PD cases group and 50 dogs in the control group. In this study were detected and characterized eight new single nucleotide variations in the dog LTF gene. Genotype and allele frequencies of these variations showed no statistically significant differences between the control and PD cases groups. Our data do not give evidence for the contribution of these LTF variations to the genetic background of canine PD. Nevertheless, the sequence variant L/15_g.411C > T leads to an aminoacid change (Proline to Leucine) and was predicted to be possibly damaging to the LTF protein. Further investigations would be of extreme value to clarify the biological importance of these new findings.

Download full-text PDF

Source
http://dx.doi.org/10.1007/s11033-011-1259-3DOI Listing

Publication Analysis

Top Keywords

ltf gene
12
periodontal disease
8
genetic
5
variations
5
ltf
5
analysis lactotransferrin
4
gene
4
lactotransferrin gene
4
gene variants
4
variants case-control
4

Similar Publications

Using BW25113 as a host, we isolated a novel lytic phage from the commercial poly-specific therapeutic phage cocktail Sextaphage (Microgen, Russia). We provide genetic and phenotypic characterization of the phage and describe its host range on the ECOR collection of reference strains. The phage, hereafter named Sxt1, is a close relative of classical coliphage T3 and belongs to the genus, yet its internal virion proteins, forming an ejectosome, differ from those of T3.

View Article and Find Full Text PDF

Unveiling the shared genes between systemic sclerosis and lung cancer.

Front Med (Lausanne)

December 2024

Department of Rheumatology and Immunology, The Affiliated Huai'an Hospital of Xuzhou Medical University, The Second People's Hospital of Huai'an, Huai'an, China.

The risk of lung cancer is significantly increased in patients with systemic sclerosis (SSc), yet the specific genes underlying this association remain unexplored. Our study aims to identify genes shared by SSc and lung cancer. We identified differentially expressed genes (DEGs) from SSc and lung adenocarcinoma (LUAD) datasets (SSc: GSE95065, LUAD: GSE136043) in the GEO database.

View Article and Find Full Text PDF
Article Synopsis
  • Atopic dermatitis (AD) and type 2 diabetes mellitus (T2DM) are different conditions, but this study reveals shared molecular mechanisms and chronic inflammation connecting them.
  • Using advanced analyses, researchers identified key genes like LTF, LTB4R, and CCR1 that are upregulated in both diseases, suggesting they could be used as biomarkers.
  • Additionally, potential therapeutic candidates Dioscin, Camptothecin, and Albamycin were found to bind effectively to CCR1, highlighting new avenues for treatment.
View Article and Find Full Text PDF

Objective: Multiple Sclerosis (MS) is an autoimmune disorder characterized by demyelination occurring within the white matter of the central nervous system. While its pathogenesis is intricately linked with the body's immune response, the precise underlying mechanisms remain elusive. This study aims to explore potential immune-related genes associated with MS and assess the causal relationship between these genes and the risk of developing MS.

View Article and Find Full Text PDF

Objective: Severe asthma (SA) is a serious disease with limited treatment options, which is closely linked to immune dysfunction. Therefore, immune-associated biomarkers may diagnose SA and offer therapeutic targets for SA.

Methods: The gene expression profiles of SA patients and matched controls were from the National Center for Biotechnology Information database.

View Article and Find Full Text PDF

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!