Rawat D S, Lumb V, Sharma Y D, Pasha S T, Singh G
Division of Biochemistry & Biotechnology, National Institute of Communicable Diseases, Delhi.
J Commun Dis. 2007 Jun;39(2):119-28.
Malaria continues to be a major cause of mortality and morbidity in tropical countries and affecting around 100 countries of the world. As per WHO estimates, 300-500 million are being infected and 1-3 million deaths annually due to malaria. With the emerging knowledge about genome sequence of all the three counterparts involved in the disease of malaria, the parasite Plasmodium, vector Anopheles and host Homo sapien have helped the scientists to understand interactions between them. Simultaneous advancement in technology further improves the prospects to discover new targets for vaccines and drugs. Though the malaria vaccine is still far away in this situation there is need to develop a potent and affordable drug(s). Histones are the key protein of chromatin and play an important role in DNA packaging, replication and gene expression. They also show frequent post-translation modifications. The specific combinations of these posttranslational modifications are thought to alter chromatin structure by forming epigenetic bar codes that specify either transient or heritable patterns of genome function. Chromatin regulators and upstream pathways are therefore seen as promising targets for development of therapeutic drugs.
疟疾仍然是热带国家死亡和发病的主要原因,影响着世界上约100个国家。根据世界卫生组织的估计,每年有3亿至5亿人感染疟疾,100万至300万人死于疟疾。随着对参与疟疾疾病的所有三个相关部分(疟原虫、媒介按蚊和宿主智人)基因组序列的新认识,科学家们得以了解它们之间的相互作用。技术的同步进步进一步改善了发现疫苗和药物新靶点的前景。尽管在这种情况下疟疾疫苗仍遥不可及,但仍需要开发有效且价格合理的药物。组蛋白是染色质的关键蛋白质,在DNA包装、复制和基因表达中起重要作用。它们还经常发生翻译后修饰。这些翻译后修饰的特定组合被认为通过形成表观遗传条形码来改变染色质结构,这些条形码指定了基因组功能的瞬时或可遗传模式。因此,染色质调节剂和上游途径被视为开发治疗药物的有希望的靶点。