Department of Agricultural Biotechnology, Assam Agricultural University, Jorhat 785013, Assam, India.
Department of Agricultural Biotechnology, Assam Agricultural University, Jorhat 785013, Assam, India.
Gene. 2014 Mar 10;537(2):333-42. doi: 10.1016/j.gene.2014.01.010. Epub 2014 Jan 13.
The endogenous small non-coding functional microRNAs (miRNAs) are short in size, range from ~21 to 24 nucleotides in length, play a pivotal role in gene expression in plants and animals by silencing genes either by destructing or blocking of translation of homologous mRNA. Although various high-throughput, time consuming and expensive techniques like forward genetics and direct cloning are employed to detect miRNAs in plants but comparative genomics complemented with novel bioinformatic tools pave the way for efficient and cost-effective identification of miRNAs through homologous sequence search with previously known miRNAs. In this study, an attempt was made to identify and characterize conserved miRNAs in garlic expressed sequence tags (ESTs) through computational means. For identification of novel miRNAs in garlic, a total 3227 known mature miRNAs of plant kingdom Viridiplantae were searched for homology against 21,637 EST sequences resulting in identification of 6 potential miRNA candidates belonging to 6 different miRNA families. The psRNATarget server predicted 33 potential target genes and their probable functions for the six identified miRNA families in garlic. Most of the garlic miRNA target genes seem to encode transcription factors as well as genes involved in stress response, metabolism, plant growth and development. The results from the present study will shed more light on the understanding of molecular mechanisms of miRNA in garlic which may aid in the development of novel and precise techniques to understand some post-transcriptional gene silencing mechanism in response to stress tolerance.
内源性小非编码功能性 microRNAs(miRNAs)大小较短,长度约为 21 到 24 个核苷酸,通过破坏或阻止同源 mRNA 的翻译来沉默基因,在动植物基因表达中发挥关键作用。尽管采用了正向遗传学和直接克隆等各种高通量、耗时且昂贵的技术来检测植物中的 miRNAs,但比较基因组学与新的生物信息学工具相结合,为通过同源序列搜索以前已知的 miRNAs 来有效且经济高效地鉴定 miRNAs 铺平了道路。在这项研究中,尝试通过计算手段鉴定和表征大蒜表达序列标签(EST)中的保守 miRNAs。为了在大蒜中鉴定新的 miRNAs,在 21637 个 EST 序列中搜索了植物界 Viridiplantae 的总共 3227 个已知成熟 miRNAs 的同源性,鉴定出 6 个潜在的 miRNA 候选物,属于 6 个不同的 miRNA 家族。psRNATarget 服务器预测了 33 个潜在的靶基因及其在大蒜中六个鉴定 miRNA 家族中的可能功能。大蒜 miRNA 靶基因的大多数似乎编码转录因子以及参与应激反应、代谢、植物生长和发育的基因。本研究的结果将更深入地了解大蒜中 miRNA 的分子机制,这可能有助于开发新的和精确的技术来理解一些转录后基因沉默机制以响应胁迫耐受性。