用聚合酶链反应鉴定新制备的布氏锥虫表达文库的编码序列。

International journal of biochemistry and molecular biology Pub Date : 2013-07-29 Print Date: 2013-01-01
Uthman Okalang, Ann Nanteza, Enock Matovu, George W Lubega
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引用次数: 0

摘要

非洲动物锥虫病(AAT)也被称为那加纳病,是撒哈拉以南非洲大部分地区家畜中的一种毁灭性疾病,造成牛奶和肉类生产以及牵引力的损失。然而,目前还没有针对AAT的商业疫苗。这些寄生虫还对一些正在使用的药物产生了耐药性。此外,发展中国家尚未充分探索使用负担得起的计算机辅助湿工作台方法寻找针对这种疾病的疫苗和(或)新药物靶点。因此,本研究探索了利用PCR技术筛选新鲜制备的布氏锥虫血流表达文库的编码序列,然后进行生物信息学分析,明确这些蛋白质对寄生虫生存的功能和重要性。从29个纯化克隆中鉴定出11个蛋白质编码序列。推测的逆转录转座子热点蛋白4 (rhsp4)是唯一具有完整注释DNA序列的蛋白。所有其他的都是假设性的,或者有部分或不合格的注释。rhsp4和丙酮酸脱氢酶E1组分α亚基(PDE1α)参与有氧呼吸,而琥珀酰co A-3酮酸辅酶A转移酶线粒体前体(SKTMP)参与酮体分解代谢。半胱氨酸-合成酶(CBS)和α -1,3-甘露糖基转移酶(αMT)分别参与了半胱氨酸的生物合成和囊泡转运。所遇到的假设蛋白质的功能既没有实验确定也没有预测。我们假设CBS和PDE1α都是很好的药物靶点。总的来说,在大约8个月的时间里,大约需要300个板来对整个布氏锥虫基因组进行PCR筛选。因此,在发展中国家资源有限的条件下,这种方法在寻找新的药物靶点方面是适用的和负担得起的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Identification of coding sequences from a freshly prepared Trypanosoma brucei brucei expression library by polymerase chain reaction.

Animal African trypanosomiasis (AAT) also known as Nagana is a devastating disease among domestic animals in large parts of Sub-Saharan Africa causing loses in milk and meat production as well as traction power. However, there is currently no commercial vaccine against AAT. The parasites have also developed resistance to some of the drugs in use. Moreover, the use of affordable computer-aided wet bench methods in the search for vaccine and/or new drug targets against this disease have not yet been fully explored in developing countries. This study, therefore, explored the use of PCR to screen a freshly prepared bloodstream form Trypanosoma brucei brucei (T. b. brucei) expression library for coding sequences followed by bioinformatics analyses specifying the functions and importance of these proteins to parasite survival. Eleven protein coding sequences were identified from twenty nine purified clones. The putative retro transposon hot spot protein 4 (RHSP 4) was the only protein with a fully annotated DNA sequence. All the others were hypothetical or had partial or unqualified annotations. RHSP 4 and pyruvate dehydrogenase E1 component, alpha sub-unit (PDE1α) are involved in aerobic respiration whereas succinyl-Co A-3-ketoacid-coenzyme A transferase mitochondrial precursor (SKTMP) is predicted to be involved in ketone body catabolism. Cystathionine beta-synthase (CBS) and alpha-1,3-mannosyltransferase (αMT) have been predicted in cysteine biosynthesis and vesicular transport respectively. The functions of the hypothetical proteins encountered have neither been experimentally determined nor predicted. We hypothesize that both CBS and PDE1α are good drug targets. Overall, about 300 plates are required to PCR screen the entire Trypanosoma brucei genome in approximately eight months. This method is therefore, applicable and affordable in the search for new drug targets under conditions of limited resources among developing countries.

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