Wei Zunzheng, Sun Zhenzhen, Cui Binbin, Zhang Qixiang, Xiong Min, Wang Xian, Zhou Di
Beijing Key Laboratory of Ornamental Plants Germplasm Innovation & Molecular Breeding, National Engineering Research Center for Floriculture and College of Landscape Architecture, Beijing Forestry University, Beijing, China.
Key Laboratory of Biology and Genetic Improvement of Horticultural Crops (North China), Ministry of Agriculture, Key Laboratory of Urban Agriculture (North), Ministry of Agriculture, Beijing Vegetable Research Center, Beijing Academy of Agriculture and Forestry Sciences, Beijing, China.
PeerJ. 2016 Sep 1;4:e2378. doi: 10.7717/peerj.2378. eCollection 2016.
Colored calla lily is the short name for the species or hybrids in section Aestivae of genus Zantedeschia. It is currently one of the most popular flower plants in the world due to its beautiful flower spathe and long postharvest life. However, little genomic information and few molecular markers are available for its genetic improvement. Here, de novo transcriptome sequencing was performed to produce large transcript sequences for Z. rehmannii cv. 'Rehmannii' using an Illumina HiSeq 2000 instrument. More than 59.9 million cDNA sequence reads were obtained and assembled into 39,298 unigenes with an average length of 1,038 bp. Among these, 21,077 unigenes showed significant similarity to protein sequences in the non-redundant protein database (Nr) and in the Swiss-Prot, Gene Ontology (GO), Cluster of Orthologous Group (COG) and Kyoto Encyclopedia of Genes and Genomes (KEGG) databases. Moreover, a total of 117 unique transcripts were then defined that might regulate the flower spathe development of colored calla lily. Additionally, 9,933 simple sequence repeats (SSRs) and 7,162 single nucleotide polymorphisms (SNPs) were identified as putative molecular markers. High-quality primers for 200 SSR loci were designed and selected, of which 58 amplified reproducible amplicons were polymorphic among 21 accessions of colored calla lily. The sequence information and molecular markers in the present study will provide valuable resources for genetic diversity analysis, germplasm characterization and marker-assisted selection in the genus Zantedeschia.
彩色马蹄莲是马蹄莲属夏花组物种或杂交种的简称。因其美丽的佛焰苞和较长的采后寿命,它目前是世界上最受欢迎的花卉植物之一。然而,可用于其遗传改良的基因组信息很少,分子标记也很少。在此,利用Illumina HiSeq 2000仪器对彩色马蹄莲品种‘Rehmannii’进行了从头转录组测序,以产生大量转录序列。获得了超过5990万个cDNA序列读数,并组装成39298个单基因,平均长度为1038 bp。其中,21077个单基因与非冗余蛋白质数据库(Nr)、Swiss-Prot、基因本体(GO)、直系同源簇(COG)和京都基因与基因组百科全书(KEGG)数据库中的蛋白质序列具有显著相似性。此外,总共定义了117个可能调控彩色马蹄莲花佛焰苞发育的独特转录本。另外,鉴定出9933个简单序列重复(SSR)和7162个单核苷酸多态性(SNP)作为潜在分子标记。设计并选择了200个SSR位点的高质量引物,其中58个扩增出的可重复扩增子在21份彩色马蹄莲种质中具有多态性。本研究中的序列信息和分子标记将为马蹄莲属的遗传多样性分析、种质鉴定和标记辅助选择提供有价值的资源。