Data from: Generation and analysis of blueberry transcriptome sequences from leaves, developing fruit, and flower buds from cold acclimation through deacclimation
Principal Investigator(s): View help for Principal Investigator(s) US Department of Agriculture; National Agricultural Library
Version: View help for Version V1
| Name | File Type | Size | Last Modified |
|---|---|---|---|
|
|
application/vnd.openxmlformats-officedocument.wordprocessingml.document | 35.3 KB | 06/26/2026 07:47:PM |
|
|
application/vnd.openxmlformats-officedocument.spreadsheetml.sheet | 103.2 KB | 06/26/2026 11:43:AM |
|
|
application/json | 28 KB | 06/26/2026 11:43:AM |
|
|
text/html | 14.4 KB | 06/26/2026 11:43:AM |
Project Citation:
Project Description
Results: Efforts to sequence the transcriptome of the commercial highbush blueberry (Vaccinium corymbosum) cultivar Bluecrop and use the sequences to identify genes associated with cold acclimation and fruit development and develop SSR markers for mapping studies are presented here. Transcriptome sequences were generated from blueberry fruit at different stages of development, flower buds at different stages of cold acclimation, and leaves by next-generation Roche 454 sequencing. Over 600,000 reads were assembled into approximately 15,000 contigs and 124,000 singletons. The assembled sequences were annotated and functionally mapped to Gene Ontology (GO) terms. Frequency of the most abundant sequences in each of the libraries was compared across all libraries to identify genes that are potentially differentially expressed during cold acclimation and fruit development. Real-time PCR was performed to confirm their differential expression patterns. Overall, 14 out of 17 of the genes examined had differential expression patterns similar to what was predicted from their reads alone. The assembled sequences were also mined for SSRs. From these sequences, 15,886 blueberry EST-SSR loci were identified. Primers were designed from 7,705 of the SSR-containing sequences with adequate flanking sequence. One hundred primer pairs were tested for amplification and polymorphism among parents of two blueberry populations currently being used for genetic linkage map construction. The tetraploid mapping population was based on a cross between the highbush cultivars Draper and Jewel (V. darrowii is also in the background of ‘Jewel’). The diploid mapping population was based on a cross between an F1 hybrid of V. darrowii and diploid V. corymbosum and another diploid V. corymbosum. The overall amplification rate of the SSR primers was 68% and the polymorphism rate was 43%.
Conclusions: These results indicate that this large collection of 454 ESTs will be a valuable resource for identifying genes that are potentially differentially expressed and play important roles in flower bud development, cold acclimation, chilling unit accumulation, and fruit development in blueberry and related species. In addition, the ESTs have already proved useful for the development of SSR and EST-PCR markers, and are currently being used for construction of genetic linkage maps in blueberry.
Resources in this dataset:
Resource Title: 12870_2011_1018_MOESM1_ESM. File Name: 12870_2011_1018_MOESM1_ESM.XLSXResource Description: Additional file 1: Most highly abundant sequences from each of the libraries along with their number of reads/frequency of reads and predicted expression patterns across the bud time points and the fruit development stages. Approximately 30 most highly abundant sequences from each of the libraries along with their number of reads/ frequency of reads and predicted expression patterns across the bud time points (0, 397, 789, and 1333 chill hours) and fruit development stages (green, white, pink, and blue/ripe). Data supplement retrieved from https://static-content.springer.com/esm/art:10.1186/1471-2229-12-46/MediaObjects/12870_2011_1018_MOESM1_ESM.XLSX
Resource Title: 12870_2011_1018_MOESM1_ESM.
File Name: 12870_2011_1018_MOESM1_ESM.XLSX
Resource Description: Additional file 1: Most highly abundant sequences from each of the libraries along with their number of reads/frequency of reads and predicted expression patterns across the bud time points and the fruit development stages. Approximately 30 most highly abundant sequences from each of the libraries along with their number of reads/ frequency of reads and predicted expression patterns across the bud time points (0, 397, 789, and 1333 chill hours) and fruit development stages (green, white, pink, and blue/ripe).
Data supplement retrieved from https://static-content.springer.com/esm/art:10.1186/1471-2229-12-46/MediaObjects/12870_2011_1018_MOESM1_ESM.XLSX
Resource Title: Supplement S3 . File Name: 11032_2013_3_MOESM3_ESM.docxResource Description: Supplement S3 Alignment of FAD3A protein sequence of PI 85671 and Williams 82, and Weblogo image showing the conservation of the amino acid region surrounding the residue N110 Data supplement retrieved from https://static-content.springer.com/esm/art:10.1186/1471-2229-12-46/MediaObjects/12870_2011_1018_MOESM2_ESM.DOCX
Resource Title: Supplement S3 .
File Name: 11032_2013_3_MOESM3_ESM.docx
Resource Description: Supplement S3 Alignment of FAD3A protein sequence of PI 85671 and Williams 82, and Weblogo image showing the conservation of the amino acid region surrounding the residue N110
Data supplement retrieved from https://static-content.springer.com/esm/art:10.1186/1471-2229-12-46/MediaObjects/12870_2011_1018_MOESM2_ESM.DOCX
Scope of Project
Related Publications
Published Versions
Found a serious problem with the data, such as disclosure risk or copyrighted content? Let us know.
This material is distributed exactly as received from the data depositor. ICPSR has not reviewed, checked, or processed this material. For additional information about the study, please contact the investigator(s) directly. If you have questions about the accessibility of materials distributed by ICPSR or require further assistance, please visit ICPSR's Accessibility Center.