Genes involved in inflammation are within celiac disease risk loci show differential mRNA expression

Celiac disease (CD) is a chronic autoimmune disease, caused by the consumption of gluten in genetically predisposed individuals. Celiac patients develop many clinical features include; weight loss, diarrhea, and Intestinal damage, and if left untreated, CD patient may face an increased risk of malig...

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Main Author: Tahseen Yahia Keelani, Ahlam
Format: Others
Language:English
Published: Högskolan i Skövde, Institutionen för biovetenskap 2018
Subjects:
Online Access:http://urn.kb.se/resolve?urn=urn:nbn:se:his:diva-16292
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spelling ndltd-UPSALLA1-oai-DiVA.org-his-162922018-10-16T06:02:19ZGenes involved in inflammation are within celiac disease risk loci show differential mRNA expressionengTahseen Yahia Keelani, AhlamHögskolan i Skövde, Institutionen för biovetenskap2018Bioinformatics and Systems BiologyBioinformatik och systembiologiCeliac disease (CD) is a chronic autoimmune disease, caused by the consumption of gluten in genetically predisposed individuals. Celiac patients develop many clinical features include; weight loss, diarrhea, and Intestinal damage, and if left untreated, CD patient may face an increased risk of malignancies. Materials and methods403 patient were admitted to the study. These patients were divided into three groups; celiac cases, controls, and latent celiac cases. Gene expression analysis was performed for intestinal biopsies and blood samples (leukocytes) using a quantitative PCR technique. The second section of the study was studying the effect of PRODH enzyme on Drosophila Melanogaster intestines. To achieve that PRODH enzyme and different amino acids were added to the fly food.  One way ANOVA and Wilcoxon tests were applied to find out the significant genes. ResultsMost of the differentially expressed genes in celiac disease are involved in the inflammatory response. However, many genes have significantly altered expression in the latent celiac group but not altered significantly in CD group. These genes are CXCL1, IL15RA, IL2RB, MAPK11, and TGM2. They are involved in the TNF signaling pathway and in inflammatory cytokines. It was noticed that in celiac disease there is a significant alteration in PRODH expression in the intestines, and the addition of PRODH enzyme to glutamine has a similar effect on the intestinal gene expression as gluten does. ConclusionWe can conclude that Non-HLA genes are important in activating the immune system, increasing proline level, and developing the clinical features of celiac disease. Secondly,  Proline metabolism has an important role in tumor suppression and in augmenting tumor growth, which makes it an important therapeutic target in tumor therapy. Student thesisinfo:eu-repo/semantics/bachelorThesistexthttp://urn.kb.se/resolve?urn=urn:nbn:se:his:diva-16292application/pdfinfo:eu-repo/semantics/openAccess
collection NDLTD
language English
format Others
sources NDLTD
topic Bioinformatics and Systems Biology
Bioinformatik och systembiologi
spellingShingle Bioinformatics and Systems Biology
Bioinformatik och systembiologi
Tahseen Yahia Keelani, Ahlam
Genes involved in inflammation are within celiac disease risk loci show differential mRNA expression
description Celiac disease (CD) is a chronic autoimmune disease, caused by the consumption of gluten in genetically predisposed individuals. Celiac patients develop many clinical features include; weight loss, diarrhea, and Intestinal damage, and if left untreated, CD patient may face an increased risk of malignancies. Materials and methods403 patient were admitted to the study. These patients were divided into three groups; celiac cases, controls, and latent celiac cases. Gene expression analysis was performed for intestinal biopsies and blood samples (leukocytes) using a quantitative PCR technique. The second section of the study was studying the effect of PRODH enzyme on Drosophila Melanogaster intestines. To achieve that PRODH enzyme and different amino acids were added to the fly food.  One way ANOVA and Wilcoxon tests were applied to find out the significant genes. ResultsMost of the differentially expressed genes in celiac disease are involved in the inflammatory response. However, many genes have significantly altered expression in the latent celiac group but not altered significantly in CD group. These genes are CXCL1, IL15RA, IL2RB, MAPK11, and TGM2. They are involved in the TNF signaling pathway and in inflammatory cytokines. It was noticed that in celiac disease there is a significant alteration in PRODH expression in the intestines, and the addition of PRODH enzyme to glutamine has a similar effect on the intestinal gene expression as gluten does. ConclusionWe can conclude that Non-HLA genes are important in activating the immune system, increasing proline level, and developing the clinical features of celiac disease. Secondly,  Proline metabolism has an important role in tumor suppression and in augmenting tumor growth, which makes it an important therapeutic target in tumor therapy.
author Tahseen Yahia Keelani, Ahlam
author_facet Tahseen Yahia Keelani, Ahlam
author_sort Tahseen Yahia Keelani, Ahlam
title Genes involved in inflammation are within celiac disease risk loci show differential mRNA expression
title_short Genes involved in inflammation are within celiac disease risk loci show differential mRNA expression
title_full Genes involved in inflammation are within celiac disease risk loci show differential mRNA expression
title_fullStr Genes involved in inflammation are within celiac disease risk loci show differential mRNA expression
title_full_unstemmed Genes involved in inflammation are within celiac disease risk loci show differential mRNA expression
title_sort genes involved in inflammation are within celiac disease risk loci show differential mrna expression
publisher Högskolan i Skövde, Institutionen för biovetenskap
publishDate 2018
url http://urn.kb.se/resolve?urn=urn:nbn:se:his:diva-16292
work_keys_str_mv AT tahseenyahiakeelaniahlam genesinvolvedininflammationarewithinceliacdiseaserisklocishowdifferentialmrnaexpression
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