Genetic variations in the PSMA3, PSMA6 and PSMC6 genes are associated with type 1 diabetes in Latvians and with expression level of number of UPS-related and T1DM-susceptible genes in HapMap individuals

2015 ◽  
Vol 291 (2) ◽  
pp. 891-903 ◽  
Author(s):  
Tatjana Sjakste ◽  
Natalia Paramonova ◽  
Kristine Osina ◽  
Kristine Dokane ◽  
Jelizaveta Sokolovska ◽  
...  
2012 ◽  
Vol 2012 ◽  
pp. 1-6 ◽  
Author(s):  
Bei Han ◽  
Xing Shi ◽  
Quan Peng ◽  
Wentao Gao

Genetic susceptibility plays a key role in type 1 diabetes development. Because miR-541 gene was located within the associated chromosome loci and its target genes include the diabetes-associated gene neurogenin3, this study aimed to investigate whether miR-541 had type 1 diabetes-associated genetic variations. Type 1 diabetes children and healthy volunteers were recruited; direct sequencing was performed in initial 69 patients and 46 volunteers. We identified 1 reported SNP (rs12893725) and 3 novel genetic variations, for the candidate -404 G→T variation, restriction fragment length polymorphism (RFLP) was performed in total 247 diabetes children and 212 healthy volunteers, a different distribution trait of allele frequencies was found between the two groups, and further clinical analysis found no significant correlation between clinical parameter and genotypes among patients. In addition, by luciferase reporter assay, -404 was found to be within putative promoter region of pre-miR-541; although mutation of G→T has no effect on promoter activity, a significant secondary structure alteration may possibly influence its processing and transcription. In conclusion, we identified 3 novel genetic variations in putative promoter of miR-541 in type 1 diabetes patients; -404 G→T of miR-541 is a potential T1D-associated genetic variation.


2021 ◽  
Author(s):  
Reza Bayat ◽  
Zivar Salehi ◽  
Setila Dalili ◽  
Farbod Bahreini

Abstract BackgroundMicroRNAs (miRNAs) are small non-coding RNA molecules that play a pivotal role in the central dogma of molecular biology by regulating gene expression. Alterations in the expression pattern of miRNAs are seen to be linked with several human diseases including autoimmune diseases such as pediatric type 1 diabetes mellitus (T1DM). Single nucleotide polymorphism (SNP) of the miRNAs coding genes can influence pancreatic development and insulin secretion. We contemplated a relation between miR-21 expression level as well as miR-21 rs1292037 SNP and pediatric T1DM.ResultsThe heterozygous T/C genotype was seen to be more common amongst T1DM patients than amongst controls (OR = 2.74 (1.78-4.27), P<0.0001). The C allele was more frequent in patients than in control subjects (OR = 1.36 (1.03-0.8), P = 0.02). miR-21 expression was seen to be upregulated in patients compared to the controls by more than twofold (p<0.0001). In the study population, miR-21 was found to be significantly upregulated when carrying the T/C genotype. ConclusionsWe report that the miR-21 rs1292037 variant is related to T1DM. Our study also suggests that the miR-21 expression level is upregulated in T1DM patients compared to the control subjects.


2006 ◽  
Vol 40 (10) ◽  
pp. 56
Author(s):  
BRUCE JANCIN
Keyword(s):  

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