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Identification of differentially expressed genes in the growth plate of broiler chickens with thiram-induced tibial dyschondroplasia

机译:锡兰诱导的胫骨软骨发育不良的肉鸡生长板中差异表达基因的鉴定

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摘要

Tibial dyschondroplasia (TD) is characterized by expansion of the proximal growth plates of the tibiotarsus that fail to form bone, lack blood vessels, and contain non-viable cells. Thiram (a carbamate pesticide), when fed to young broiler chicks, induces TD with high regularity and precision. We used this experimental model to understand the cause of the defects associated with TD by selecting and identifying the genes differentially expressed in the TD growth plate of broiler chickens. Broiler chicks at 7 days of age were randomly divided into two groups. After fasting overnight, they were fed with regular diet (control) or the same diet containing 100 mg/kg thiram for 96 h to induce TD (thiram-fed). mRNA was purified from the growth plates of control and thiram-fed broilers. Forward and reverse-subtracted cDNA libraries were generated by suppression subtractive hybridization technology. Ten selected genes from cDNA libraries were identified by real-time quantitative polymerase chain reaction. All were differentially expressed in TD growth plates (P<0.05 or P<0.01). The levels of collagen type X (Col X), pro-alpha-1 collagen type I (Col I α1), collagen type IX (Col IX), NADH dehydrogenase (NADH DH), cytochrome C oxidase subunit III (COX III), enolase 1, alpha (ENO1), carbonic anhydrase II (CA2) and heat shock protein 90 (Hsp90) mRNA transcripts were up-regulated, while the expression levels of Matrilin 3 (MATN3) and chondromodulin-I (ChM-I) were down-regulated. Col I and Hsp90 were detected by immunohistochemistry at different stages. Given that these genes are involved in matrix formation, endochondral ossification, developmental regulation, electron transport in the mitochondrial respiratory chain and vascularization, our findings may provide new insights into understanding the pathogenesis of TD.
机译:胫骨软骨发育不良(TD)的特征是胫骨tar骨的近端生长板扩张,无法形成骨骼,缺乏血管并包含无活力的细胞。当将Thiram(一种氨基甲酸酯杀虫剂)喂给雏鸡时,它能以高规律性和精确度诱导TD。我们通过选择和鉴定肉鸡TD生长板中差异表达的基因,使用该实验模型来了解与TD相关的缺陷的原因。将7日龄的小鸡随机分为两组。禁食过夜后,给他们喂以常规饮食(对照)或含有100 mg / kg锡拉姆的相同饮食,持续96小时以诱导TD(锡拉姆喂养)。从对照和硫胺素肉鸡的生长板中纯化mRNA。通过抑制消减杂交技术产生正向和反向扣除的cDNA文库。通过实时定量聚合酶链反应鉴定了从cDNA文库中选择的10个基因。均在TD生长平板中差异表达(P <0.05或P <0.01)。 X型胶原蛋白(Col X),pro-alpha-1 I型胶原蛋白(Col Iα1),IX型胶原蛋白(Col IX),NADH脱氢酶(NADH DH),细胞色素C氧化酶亚基III(COX III)的水平),烯醇酶1,α(ENO1),碳酸酐酶II(CA2)和热休克蛋白90(Hsp90)mRNA转录上调,而基质胶3(MATN3)和软骨调节蛋白I(ChM-1)的表达水平被下调了。通过免疫组织化学在不同阶段检测Col I和Hsp90。鉴于这些基因参与基质形成,软骨内骨化,发育调节,线粒体呼吸链中的电子运输和血管形成,我们的发现可能为理解TD的发病机理提供新的见解。

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    《Avian Pathology》 |2009年第2期|p.161-166|共6页
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    State Key Laboratory of Agricultural Microbiology, College of Veterinary Medicine, Huazhong Agricultural University, Wuhan, 430070, China;

    Shanxi Agricultural University, College of Animal Science and Technology, Taigu, Shanxi, 030801, China;

    Huazhong A;

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