首页> 外文期刊>Journal of dairy science >Real-Time PCR Quantification of Bovine Lactase mRNA: Localization in the Gastrointestinal Tract of Milk-Fed Calves
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Real-Time PCR Quantification of Bovine Lactase mRNA: Localization in the Gastrointestinal Tract of Milk-Fed Calves

机译:牛乳糖酶mRNA的实时PCR定量:牛奶喂养犊牛胃肠道中的定位。

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Lactase is a disaccharidase that is present in the brush-border membrane of the small intestine, hydro-lyzes lactose to glucose and galactose, and is therefore important in milk-fed animals. Assays based on quantitative real-time reverse transcription-polymerase chain reaction (RT-PCR) in the bovine species have not yet been described. Therefore, we have developed an RT-PCR assay for the quantification of lactase mRNA levels and have tested its suitability in the bovine gastrointestinal tract of seven 5-d-old milk-fed calves. Primers for RT-PCR amplification of bovine lactase mRNA were designed in the 100% identical regions of species (rats, rabbits, humans) from which lactase sequences were available. Lactase mRNA was expressed relative to mean levels of 4 housekeeping genes (glyceraldehyde-3-phosphate dehydrogenase, β-actin, ubiquitin, and 18S). The presence of lactase mRNA along the entire gastrointestinal tract was evaluated in samples that consisted of whole gut walls (mucosa plus submucosa). Furthermore, mRNA levels of lactase were measured in fractionized layers of jeju-nal and ileal mucosa (mainly containing villus tips or crypts) and ileal lamina propria (mainly containing Peyer's patches). Agarose gel electrophoresis of the lactase PCR product revealed a single band that corresponded to the single-amplified product as predicted by the melting curve analysis of the PCR. The amplified partial-bovine lactase sequence showed 87% similarity with human and rabbit sequences and 82% similarity with the rat sequence. Lactase mRNA was present in whole walls (consisting of mucosa and submucosa) of the entire small intestine, but was absent in esophagus, rumen, fundus, pylorus, and colon. Furthermore, lactase mRNA was detected in fractionized villus and crypt layers of jejunum and ileum, but levels were higher in the jejunum in villus than in crypt fractions. No lactase mRNA was detectable in the lamina propria fraction of the ileum containing mainly Peyer's patches. In conclusion, the developed RT-PCR method allows study of lactase mRNA levels.
机译:乳糖酶是存在于小肠刷状边界膜上的一种双糖酶,可将乳糖水解为葡萄糖和半乳糖,因此在喂奶的动物中很重要。尚未描述基于牛物种中实时定量逆转录聚合酶链反应(RT-PCR)的检测方法。因此,我们开发了一种定量定量乳糖酶mRNA水平的RT-PCR分析方法,并测试了其在7头5 d龄奶牛犊的牛胃肠道中的适用性。在可获得乳糖酶序列的物种(大鼠,兔子,人类)的100%相同区域中设计了用于牛乳糖酶mRNA的RT-PCR扩增的引物。相对于四个管家基因(甘油醛-3-磷酸脱氢酶,β-肌动蛋白,泛素和18S)的平均水平,表达了乳糖酶mRNA。在整个肠壁(粘膜和粘膜下层)组成的样品中评估了整个胃肠道中乳糖酶mRNA的存在。此外,在空肠和回肠粘膜(主要包含绒毛尖端或隐窝)和回肠固有层(主要包含Peyer's贴片)的分层中测量了乳糖酶的mRNA水平。乳糖酶PCR产物的琼脂糖凝胶电泳显示一条条带,该条带对应于PCR的解链曲线分析所预测的单扩增产物。扩增的部分牛乳糖酶序列与人和兔序列具有87%的相似性,与大鼠序列具有82%的相似性。乳糖酶mRNA存在于整个小肠的整个壁(由粘膜和粘膜下层组成)中,但在食道,瘤胃,眼底,幽门和结肠中不存在。此外,在空肠和回肠的分离的绒毛和隐窝层中检测到乳糖酶mRNA,但是绒毛中的空肠中的乳糖酶水平高于隐窝部分。在回肠的固有层部分中,主要包含派伊尔斑块的未检测到乳糖酶mRNA。总之,开发的RT-PCR方法可以研究乳糖酶mRNA的水平。

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