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پژوهش های علوم دامی، جلد ۳۴، شماره ۲، صفحات ۳۱-۴۴

عنوان فارسی مطالعه جامع ژن‌های غیرکدکننده بلند مرتبط با سندرم آسیت طیور
چکیده فارسی مقاله اهداف: سندرم آسیت ، عارضه‌ای است که معمولا، در جوجه‌های گوشتی در حال رشد در تمام نقاط دنیا رخ می-دهد واین بیماری یکی از علل مهم تلفات در بسیاری از گله‌ها می‌باشد. درسبب‌شناسی این عارضه درپرندگان حساس نسبت به پرندگان مقاوم، علاوه بر فاکتور‌های محیطی، پروفایل بیان متفاوت ژن‌ها احتمالا، در حین یا قبل از بروز بیماری دخیل می‌باشد. همچنین، عامل این تفاوت بیان ژن، ممکن است تحت تاثیر RNAهای غیرکدکننده طویل باشد. لذا هدف از تحقیق حاضر، شناسایی و کشف ژن‌های غیرکدکننده بلند طولانی موثر برسندرم آسیت در جوجه‌های گوشتی بود.
مواد و روش‌ها: بدین منظور، از شش مجموعه داده متعلق به چهاربافت (کبد، کلیه، قلب و سرخرگ ششی) استفاده شد. جهت شناسایی ژن‌های غیرکدکننده بلند طولانی از انواع نرم‌افزارها (CPC2, CNIT PLEK, FEELNC, PLIT) و انواع بلاستها بر علیه پایگاه داده های مختلف NR و Refseq و همچنین، سایر ابزارهای شناسایی رونوشت‌ها استفاده شد. برای انجام متاآنالیز ازنرم‌افزار meta-RNAseq و روش فیشر استفاده شد.
یافته‌ها: بررسی نتایج این تحقیق نشان داد که 188 رونوشت lncRNA به عنوان RNA غیرکدکننده بلند طولانی جدید در بافت‌های مورد بررسی کشف و شناسایی شدند. از این تعداد، 166 lncRNA در فاصله 50±هزار بازنوکلئوتیدی با 689 تعداد ژن همجوار بودند. آنالیز همبیانی نشان داد که بین 13عدد lncRNA وتعداد 17 ژن همجوار همبستگی بالای 90/0 وجود داشت. از این 17تعداد ژن همجوار،6 تعداد ژن کدکننده شناخته شده بودند. بررسی سطح معنی‌داری بین گروه پرندگان سالم و آسیتی نشان داد که در بافت سرخرگ ششی بیان 4 ژن به صورت معنی داری متفاوت بود که این 4 ژن همجوار کدکننده با3 تا lncRNA ارتباط بیانی داشتند. بعبارت دیگر، یک lncRNA دو ژن همجوار را کنترل می‌کرد. درمتاآنالیز نیز تعداد 9 ژن lncRNA بین پرندگان سالم و آسیتی بطور معنی داری دارای بیان افتراقی بود که بررسی های بیشتر آنها نشان دهنده ارتباطات آنها با سندروم آسیت بود.
نتیجه گیری: نتایج این تحقیق به روشنی نشان داد که lncRNA ها نقش مهمی در بروز بیماری آسیت ایفا می-کنند و با مدیریت ژنتیکی گله‌های مرغان تجاری می‌توان بروز این عارضه در مرغداری‌ها را کم و ضررهای اقتصادی را کنترل کرد.
واژه‌های کلیدی: آسیت، متاآنالیز، RNAهای غیرکدکننده بلند طولانی، فیشر
کلیدواژه‌های فارسی مقاله آسیت، متاآنالیز، RNAهای غیرکدکننده بلند طولانی، فیشر،

عنوان انگلیسی A comprehensive study of long noncoding genes associated with ascites syndrome in poultry
چکیده انگلیسی مقاله Objectives Objectives: Ascites syndrome occurs in growing broilers in all parts of the world and is a major cause of losses in many flocks. In addition to genetic and non-genetic factors, differential expression of genes in susceptible chickens compared to resistant chickens during or before onset of the disease is likely involved. This difference in gene expression can be influenced by long non-coding RNAs. Therefore, the aim of this research was to identify and discover long non-coding genes effective in ascites syndrome in four tissues of broilers.Ascites.
Materials and methods: Six data sets in four tissues (liver, kidney, heart and pulmonary artery) were used for this research. Hisat2 software was used to align the reads with chicken reference genome and Sting Tie software package was used to assemble the transcripts. To identify long non-coding genes, we used various software (CPC2, CNIT PLEK, FEELNC, PLIT) and BLAST methods. meta-RNAseq software and Fisher's method were used to perform meta-analysis.
Results: Examination of the results of this research revealed that 188 lncRNAs were detected in the examined tissues and identified as new long non-coding RNAs. Of these, 160 lncRNAs were located within 50,000 contiguous 689 genes. Coexpression analysis showed that there was a correlation of 0.9 between 13 lncRNAs and 17 neighboring genes. Of these 17 neighboring genes, 6 coding genes were known. Examination of the level of significance between the healthy group and the ascites group in the examined tissues showed that in the pulmonary artery tissue the expression of 4 genes was significantly different and these 4 adjacent coding genes with 3 lncRNAs, i.e. H. an lncRNA that controls two adjacent genes. In the meta-analysis, 9 lncRNA genes were differentially expressed between healthy chickens and ascites chickens.
Conclusion: The results of this research showed that lncRNAs play an important role in the
occurrence of ascites disease and that genetic management can reduce the occurrence of this
complication in poultry farms and control economic losses.
Key words: Ascites, Fisher, Long non-coding RNAs, Meta-analysis

Objectives Objectives: Ascites syndrome occurs in growing broilers in all parts of the world and is a major cause of losses in many flocks. In addition to genetic and non-genetic factors, differential expression of genes in susceptible chickens compared to resistant chickens during or before onset of the disease is likely involved. This difference in gene expression can be influenced by long non-coding RNAs. Therefore, the aim of this research was to identify and discover long non-coding genes effective in ascites syndrome in four tissues of broilers.Ascites.
Materials and methods: Six data sets in four tissues (liver, kidney, heart and pulmonary artery) were used for this research. Hisat2 software was used to align the reads with chicken reference genome and Sting Tie software package was used to assemble the transcripts. To identify long non-coding genes, we used various software (CPC2, CNIT PLEK, FEELNC, PLIT) and BLAST methods. meta-RNAseq software and Fisher's method were used to perform meta-analysis.
Results: Examination of the results of this research revealed that 188 lncRNAs were detected in the examined tissues and identified as new long non-coding RNAs. Of these, 160 lncRNAs were located within 50,000 contiguous 689 genes. Coexpression analysis showed that there was a correlation of 0.9 between 13 lncRNAs and 17 neighboring genes. Of these 17 neighboring genes, 6 coding genes were known. Examination of the level of significance between the healthy group and the ascites group in the examined tissues showed that in the pulmonary artery tissue the expression of 4 genes was significantly different and these 4 adjacent coding genes with 3 lncRNAs, i.e. H. an lncRNA that controls two adjacent genes. In the meta-analysis, 9 lncRNA genes were differentially expressed between healthy chickens and ascites chickens.
Conclusion: The results of this research showed that lncRNAs play an important role in the
occurrence of ascites disease and that genetic management can reduce the occurrence of this
complication in poultry farms and control economic losses.
Key words: Ascites, Fisher, Long non-coding RNAs, Meta-analysis

Objectives Objectives: Ascites syndrome occurs in growing broilers in all parts of the world and is a major cause of losses in many flocks. In addition to genetic and non-genetic factors, differential expression of genes in susceptible chickens compared to resistant chickens during or before onset of the disease is likely involved. This difference in gene expression can be influenced by long non-coding RNAs. Therefore, the aim of this research was to identify and discover long non-coding genes effective in ascites syndrome in four tissues of broilers.Ascites.
Materials and methods: Six data sets in four tissues (liver, kidney, heart and pulmonary artery) were used for this research. Hisat2 software was used to align the reads with chicken reference genome and Sting Tie software package was used to assemble the transcripts. To identify long non-coding genes, we used various software (CPC2, CNIT PLEK, FEELNC, PLIT) and BLAST methods. meta-RNAseq software and Fisher's method were used to perform meta-analysis.
Results: Examination of the results of this research revealed that 188 lncRNAs were detected in the examined tissues and identified as new long non-coding RNAs. Of these, 160 lncRNAs were located within 50,000 contiguous 689 genes. Coexpression analysis showed that there was a correlation of 0.9 between 13 lncRNAs and 17 neighboring genes. Of these 17 neighboring genes, 6 coding genes were known. Examination of the level of significance between the healthy group and the ascites group in the examined tissues showed that in the pulmonary artery tissue the expression of 4 genes was significantly different and these 4 adjacent coding genes with 3 lncRNAs, i.e. H. an lncRNA that controls two adjacent genes. In the meta-analysis, 9 lncRNA genes were differentially expressed between healthy chickens and ascites chickens.
Conclusion: The results of this research showed that lncRNAs play an important role in the
occurrence of ascites disease and that genetic management can reduce the occurrence of this
complication in poultry farms and control economic losses.
Key words: Ascites, Fisher, Long non-coding RNAs, Meta-analysis
کلیدواژه‌های انگلیسی مقاله آسیت, متاآنالیز, RNAهای غیرکدکننده بلند طولانی, فیشر

نویسندگان مقاله مینا آقازاده |
گروه علوم دامی دانشکده کشاورزی دانشگاه تبریز

سید عباس رافت |
گروه علوم دامی دانشگاه تبریز

آرش جوانمرد |
گروه علوم دامی دانشگاه تبریز

کریم حسن پور |
گروه علوم دامی دانشکده کشاورزی دانشگاه تبریز


نشانی اینترنتی https://animalscience.tabrizu.ac.ir/article_18750_5403e59a924ba484fd0130f94a3e3fb2.pdf
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