Design and Specificity Test of Specific Primers for Neuroglobin Gene Expression Modulation in Brain Tissue of Rattus norvegicus using qRT-PCR

IF 7.6 1区 生物学 Q1 BIOLOGY
Bintang Fadhil Ramadhan, Muhammad Farikh, Muhammad Naufal Arrafi, Nagra Aulia Valofi, Walidatul Awaliyah, Jessi Rizkanauli Simangungsong, Dini Herisanti, S. Farma
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Abstract

. Neuroglobin (Ngb) is a newly discovered globin that is found in large numbers in neurons. Brain cells are very sensitive to lack of oxygen and can begin to die within five minutes after the oxygen supply is cut off. Hypoxic conditions of brain tissue are ischemic in the area of the bleeding center This study aims to design and test the specificity of the Neuroglobin Rattus norvegicus mRNA gene in silico as a nucleotide capable of reading neuroglobin gene expression. The neuroglobin gene sequence was obtained using a "nucleotide" search menu provided by NCBI GenBank and designed using Geneious Prime bioinformatics software. The neuroglobin gene sequence used in this study was Rattus norvegicus mRNA with accession number NM_033359.3|:1-1,773. Synthesized primary pairs are optimized using PCR gradients. PCR products were analyzed by electrophoresis using 1.5% agarose gel, 100 V for 27 minutes. The results obtained one forward primer for Rattus norvegicus neuroglobin (Ngb) which has a length of 20 bases with the order of 5' AGTCTTAGCCTCTCCCCCAG -3' and reverse primer has a length of 20 bases with the order of 5' GTCTACAGAACCACGGCACAcx-3' product size 803 bp. The difference Tm in this pair of primers is 0.9 0C. The gradient PCR results showed the thickest and clearest DNA bands were at 57.7°C. Primers with the best primary criteria for neuroglobin genes were obtained with an amplicon size of 803 bp and an aneealing temperature of 57.7 °C. The design results meet the requirements of good criteria so that the primary candidate design results can be used for the PCR process.
利用 qRT-PCR 技术设计和测试用于调节鼠脑组织中神经球蛋白基因表达的特异性引物
.神经球蛋白(Ngb)是一种新发现的球蛋白,大量存在于神经元中。脑细胞对缺氧非常敏感,在氧气供应被切断后五分钟内就会开始死亡。脑组织缺氧会导致出血中枢区域缺血。本研究旨在设计和测试神经球蛋白鼠 mRNA 基因的特异性,将其作为能够读取神经球蛋白基因表达的核苷酸。神经球蛋白基因序列是通过 NCBI GenBank 提供的 "核苷酸 "搜索菜单获得的,并使用 Geneious Prime 生物信息学软件进行设计。本研究中使用的神经球蛋白基因序列为诺瓦克鼠 mRNA,登录号为 NM_033359.3|:1-1,773。利用 PCR 梯度对合成的主配对进行优化。PCR 产物经 1.5% 琼脂糖凝胶电泳分析,100 V,27 分钟。结果发现,鼠神经球蛋白(Ngb)的正向引物长度为 20 个碱基,顺序为 5' AGTCTTAGCCTCTCCCCCAG -3',反向引物长度为 20 个碱基,顺序为 5' GTCTACAGAACCACGGCACAcx-3' 产物大小为 803 bp。这对引物的 Tm 相差 0.9 摄氏度。梯度 PCR 结果显示,57.7℃ 时的 DNA 条带最粗最清晰。得到的神经球蛋白基因引物具有最佳的初选标准,其扩增片段大小为 803 bp,起始温度为 57.7 ℃。设计结果符合良好标准的要求,因此主要候选设计结果可用于 PCR 过程。
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来源期刊
BioScience
BioScience 生物-生物学
CiteScore
14.10
自引率
2.00%
发文量
109
审稿时长
3 months
期刊介绍: BioScience is a monthly journal that has been in publication since 1964. It provides readers with authoritative and current overviews of biological research. The journal is peer-reviewed and heavily cited, making it a reliable source for researchers, educators, and students. In addition to research articles, BioScience also covers topics such as biology education, public policy, history, and the fundamental principles of the biological sciences. This makes the content accessible to a wide range of readers. The journal includes professionally written feature articles that explore the latest advancements in biology. It also features discussions on professional issues, book reviews, news about the American Institute of Biological Sciences (AIBS), and columns on policy (Washington Watch) and education (Eye on Education).
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