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黑花生和粉花生中花色苷合成的比较转录组分析。

Comparative transcriptome analysis of anthocyanin synthesis in black and pink peanut.

机构信息

College of Life Sciences, Shandong Normal University, Ji'nan, China.

Biotechnology Research Center, Shandong Academy of Agricultural Sciences, Ji'nan, China.

出版信息

Plant Signal Behav. 2020;15(2):1721044. doi: 10.1080/15592324.2020.1721044. Epub 2020 Feb 2.

DOI:10.1080/15592324.2020.1721044
PMID:32009540
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7053958/
Abstract

In recent years, black testa peanut ( L.) has been favored because of its nutritional value and health function. To explore the genetic basis of peanut testa color, high-throughput sequencing technology was used to sequence the transcriptome of black testa peanut 'ZH9' and pink testa peanut 'ZH8.' Over 18 million high-quality reads were assembled into 49,404-52,578 genes for these two cultivars using a combined assembly strategy. Totally, 4,122 differentially expressed genes (DEGs) were identified between ZH8 and ZH9, among which 1317 (32%) were up-regulated and 2805 (68%) were down-regulated. KEGG analysis showed that the pathways of anthocyanin biosynthesis, isoflavonoid biosynthesis, flavone and flavonol biosynthesis, and phenylpropanoid biosynthesis were in the top 20 differentially expressed genes enriched pathways. Further analysis showed that the formation of the black color of ZH9 testa was mainly due to the reduction of lignin biosynthesis and isoflavonoid biosynthesis, and as a result, more substrate flow to anthocyanin biosynthesis. The up-regulation of all genes associated with DFR, a key enzyme determining flavonoid synthesis or anthocyanin synthesis in the flavonoid metabolic pathway, is also a strategy for increasing dihydroflavonol, a substrate for anthocyanin and flavonol biosynthesis. In addition, we identified three up-regulated R2R3MYB transcription factors associated with anthocyanin biosynthesis in ZH9. Finally, we verified the expressions of 15 genes that encode key enzymes and transcription factors using quantitative real-time PCR (qRT-PCR).

摘要

近年来,黑皮花生(L.)因其营养价值和保健功能而受到青睐。为了探索花生种皮颜色的遗传基础,本研究利用高通量测序技术对黑皮花生品种‘ZH9’和粉皮花生品种‘ZH8’的转录组进行测序。采用组合组装策略,将这两个品种的超过 1800 万个高质量reads 组装成 49404-52578 个基因。共鉴定到 4122 个差异表达基因(DEGs),其中 ZH8 和 ZH9 之间有 1317 个(32%)上调,2805 个(68%)下调。KEGG 分析表明,花色苷生物合成、异黄酮生物合成、黄酮和黄酮醇生物合成、苯丙素生物合成途径是前 20 个差异表达基因富集途径。进一步分析表明,ZH9 种皮黑色的形成主要归因于木质素生物合成和异黄酮生物合成的减少,从而使更多的底物流向花色苷生物合成。类黄酮代谢途径中决定黄酮类合成或花色苷合成的关键酶 DFR 相关所有基因的上调也是增加二氢黄酮醇(花色苷和黄酮醇生物合成的底物)的策略。此外,我们在 ZH9 中鉴定到三个与花色苷生物合成相关的上调 R2R3MYB 转录因子。最后,我们使用实时荧光定量 PCR(qRT-PCR)验证了 15 个编码关键酶和转录因子的基因的表达。

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2
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