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Transcriptional profiling of sweetpotato (Ipomoea batatas) roots indicates down-regulation of lignin biosynthesis and up-regulation of starch biosynthesis at an early stage of storage root formation

Nurit Firon1*, Don LaBonte2, Arthur Villordon3, Yanir Kfir1, Julio Solis2, Evgenia Lapis1, Temima Schnitzer Perlman4, Adi Doron-Faigenboim1, Amots Hetzroni5, Leviah Althan1 and Lahan Adani Nadir1

Author Affiliations

1 Institute of Plant Sciences, The Volcani Center, Agricultural Research Organization, Bet Dagan 50250, Israel

2 LSU AgCenter School of Plant, Environmental, and Soil Sciences, 137 J.C. Miller Hall, Baton Rouge, LA 70803-2120, USA

3 LSU AgCenter Sweet Potato Research Station, Chase, LA 71324, USA

4 Medical Goldyne Savad Institute of Gene Therapy, Hadassah Medical Center, Jerusalem 91120, Israel

5 Agricultural Engineering, Sensing, Information and Mechanization Engineering, The Volcani Center, Agricultural Research Organization, Bet Dagan 50250, Israel

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BMC Genomics 2013, 14:460  doi:10.1186/1471-2164-14-460

Published: 9 July 2013



The number of fibrous roots that develop into storage roots determines sweetpotato yield. The aim of the present study was to identify the molecular mechanisms involved in the initiation of storage root formation, by performing a detailed transcriptomic analysis of initiating storage roots using next-generation sequencing platforms. A two-step approach was undertaken: (1) generating a database for the sweetpotato root transcriptome using 454-Roche sequencing of a cDNA library created from pooled samples of two root types: fibrous and initiating storage roots; (2) comparing the expression profiles of initiating storage roots and fibrous roots, using the Illumina Genome Analyzer to sequence cDNA libraries of the two root types and map the data onto the root transcriptome database.


Use of the 454-Roche platform generated a total of 524,607 reads, 85.6% of which were clustered into 55,296 contigs that matched 40,278 known genes. The reads, generated by the Illumina Genome Analyzer, were found to map to 31,284 contigs out of the 55,296 contigs serving as the database. A total of 8,353 contigs were found to exhibit differential expression between the two root types (at least 2.5-fold change). The Illumina-based differential expression results were validated for nine putative genes using quantitative real-time PCR. The differential expression profiles indicated down-regulation of classical root functions, such as transport, as well as down-regulation of lignin biosynthesis in initiating storage roots, and up-regulation of carbohydrate metabolism and starch biosynthesis. In addition, data indicated delicate control of regulators of meristematic tissue identity and maintenance, associated with the initiation of storage root formation.


This study adds a valuable resource of sweetpotato root transcript sequences to available data, facilitating the identification of genes of interest. This resource enabled us to identify genes that are involved in the earliest stage of storage root formation, highlighting the reduction in carbon flow toward phenylpropanoid biosynthesis and its delivery into carbohydrate metabolism and starch biosynthesis, as major events involved in storage root initiation. The novel transcripts related to storage root initiation identified in this study provide a starting point for further investigation into the molecular mechanisms underlying this process.

Fibrous root; Ipomoea batatas; Lignin biosynthesis; Starch biosynthesis; Storage-root initiation; Transcription profiling