Effect of in vitro Incubation Time and Drying on Genomic DNA Extracted from Bovine Ear Tissue Samples

Tejas Gohil, Sandeep Kumar Donthula, Bhumika Parmar, Hardik Poojara, Pankaj Limbachiya, A. Sudhakar
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Abstract

Background: Use of ear punch samples as a competent source of nucleic acids from bovines, gained momentum around two decades ago, as their collection is quite easy and can be transported with minimal quantities of preservatives at ambient conditions. However, the auricular cartilage makes them more resistant to lysis, resulting in poor genomic DNA yields. The objective of the current study was to investigate whether drying can enhance the gDNA yields from ear tissue samples as a few past experiments gave an unanticipated good gDNA yields from completely dried tissue samples. Methods: Upon receipt, ear tissue samples of the cattle and buffaloes were kept at room temperature for different time intervals (in vitro incubation) and then dried at various temperatures prior to gDNA extraction, with commercially available gDNA extraction kits from two manufacturers (MN and QIAGEN). The extracted gDNA samples were assessed with spectrophotometry, flourometry and agarose gel electrophoresis for concentration, purity and integrity. Result: gDNA yields were gradually increasing in parallel to in vitro incubation time till 250 days and after that there was a decline. Further, gDNA yields were significantly higher for ear tissue samples that were not dried prior to extraction, which did not comply with the past experimental observations. Fluorometry-based quantifications revealed that drying of ear tissue samples at greater than 50°C temperatures reduced double-stranded DNA, however up to 50°C the gDNA yield increased, indicating the tissue samples can be safely transported up to 50°C in the TSUs.
体外培养时间和干燥对牛耳组织样本基因组DNA提取的影响
背景:大约在二十年前,利用耳孔样本作为牛核酸的有效来源获得了势头,因为它们的收集非常容易,并且可以在环境条件下用少量防腐剂运输。然而,耳廓软骨使它们更不易溶解,导致基因组DNA产量低。当前研究的目的是研究干燥是否可以提高耳组织样本的gDNA产量,因为过去的一些实验给出了完全干燥组织样本的意外良好的gDNA产量。方法:牛和水牛耳组织样本收到后,在室温下保存不同时间间隔(体外培养),然后在不同温度下干燥,然后使用两家制造商(MN和QIAGEN)的市购gDNA提取试剂盒提取gDNA。用分光光度法、荧光法和琼脂糖凝胶电泳对提取的dna样品进行浓度、纯度和完整性评估。结果:gDNA产率随体外培养时间的增加而逐渐增加,至250 d后呈下降趋势。此外,提取前未干燥的耳组织样品的gDNA产量显着更高,这与过去的实验观察不符。基于荧光定量分析的结果显示,在高于50°C的温度下干燥耳组织样品会减少双链DNA,但在高达50°C的温度下,gDNA产量增加,这表明组织样品可以在tsu中安全运输到50°C。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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