کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
10971739 | 1106539 | 2007 | 17 صفحه PDF | دانلود رایگان |
عنوان انگلیسی مقاله ISI
Gene polymorphisms associated with reduced hepatic expression of porcine mannan-binding lectin C
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کلمات کلیدی
RT-PCRMBLb2mMASPβ2-microglobulin - β2-میکروگلوبولینInnate immunity - ایمنی ذاتیCollectin - جمع آوری شدهMannan-binding lectin - لکتین اتصال دهنده مانانReverse-transcriptase polymerase chain reaction - واکنش زنجیره ای پلیمراز معکوس ترانس کریتازMBL-associated serine protease - پروتئاز serine مرتبط با MBLPromoter - پروموترPolymorphism - پلی مورفیسمSingle-nucleotide polymorphism - پلی مورفیسم تک نوکلئوتیدیSNP - چندریختی تک-نوکلئوتید
موضوعات مرتبط
علوم زیستی و بیوفناوری
بیوشیمی، ژنتیک و زیست شناسی مولکولی
زیست شناسی تکاملی
پیش نمایش صفحه اول مقاله

چکیده انگلیسی
Previous studies showed that low expression of mannan-binding lectin C (MBL-C) in pigs was not due to single-nucleotide polymorphisms (SNPs) in the coding region of pig MBL2. In these studies, we compared the 5â² flanking regions of porcine MBL1 (1907 bp) and MBL2 (1880 bp) in normal and diseased pigs with low or high hepatic expression of MBL2. Hepatic expression of MBL-C was very low in all pigs submitted for postmortem diagnosis. In various European pig breeds, a G(-1081)A substitution was linked to very low hepatic MBL-C expression, and was more frequent in diseased pigs. A C(â251)T substitution with less influence on MBL-C expression was more common in various breeds but was not associated with disease. MBL2 polymorphisms were associated with some disease groups and with the presence of some etiologic agents. These findings indicate that some promoter polymorphisms impair MBL-C expression in pigs and may increase their susceptibility to disease.
ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Developmental & Comparative Immunology - Volume 31, Issue 8, 2007, Pages 830-846
Journal: Developmental & Comparative Immunology - Volume 31, Issue 8, 2007, Pages 830-846
نویسندگان
Brandon N. Lillie, Natalie D. Keirstead, E. James Squires, M. Anthony Hayes,