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Comparative transcriptome analysis of latex from rubber tree clone CATAS8-79 and PR107

机译:橡胶树克隆CATAS8-79和PR107的乳胶比较转录组分析

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摘要

Rubber tree (Hevea brasiliensis Muell. Arg.) is the primary commercial source of natural rubber in the world. Latex regeneration and duration of latex flow after tapping are the two factors that determine the rubber yield of a rubber tree, and exhibit a huge variation between rubber tree clones CATAS8-79 and PR107. In the present paper, with the purpose of globally characterizing latex transcriptome, RNAs were extracted from CATAS8-79 and PR107 at first tapping and sequenced with Illumina paired-end sequencing technology individually. After excluding low-quality reads as empty adapters, 26 million clean reads were generated in both pools. Using SOAPdenove software, 296,736 and 308,262 contigs ranging from 100 bp to more than 3000 bp were assembled in CATAS8-79 and PR107 (NCBI accession numbers: GSE59981). Based on paired-end and gap-filling, 53,571 and 57,806 unigenes were generated in CATAS8-79 and PR107 individually. With the help of unigenes from two pools, it is possible to identify the longer sequence derived from the same transcript as reference transcriptome. Thus, 51,829 all-unigenes were finally integrated using paired-end joining with an average length of 640 bp and a N50 of 526 bp.
机译:橡胶树(Hevea brasiliensis Muell。Arg。)是世界上天然橡胶的主要商业来源。出胶后胶乳的再生和胶乳流动的持续时间是决定橡胶树橡胶产量的两个因素,并且在橡胶树克隆CATAS8-79和PR107之间表现出巨大的差异。在本文中,为了全局表征乳胶转录组,首先从CATAS8-79和PR107中提取RNA,并分别使用Illumina的双末端测序技术进行测序。将低质量的读取排除为空适配器后,两个池中均产生了2600万次干净读取。使用SOAPdenove软件,在CATAS8-79和PR107(NCBI登录号:GSE59981)中组装了从100bp到3000bp以上的296736和308262contig重叠群。基于配对末端和缺口填充,在CATAS8-79和PR107中分别生成了53,571和57,806个单基因。借助来自两个库的单基因,可以鉴定出源自同一转录本的较长序列作为参考转录组。因此,最终通过配对末端连接整合了51,829个全单基因,平均长度为640bp,N50为526bp。

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