Suppr超能文献

功能型 MYB 转录因子基因 HtMYB2 与菊芋花色苷生物合成相关。

Functional MYB transcription factor gene HtMYB2 is associated with anthocyanin biosynthesis in Helianthus tuberosus L.

机构信息

Academy of Agriculture and Forestry Sciences, Qinghai University, Xining, 810016, China.

Qinghai Province Key Laboratory of Vegetable Genetics and Physiology, Xining, 810016, China.

出版信息

BMC Plant Biol. 2020 Jun 1;20(1):247. doi: 10.1186/s12870-020-02463-8.

Abstract

BACKGROUND

Tuber color is an important trait for Helianthus tuberosus L. (Jerusalem artichoke). Usually, purple tubers with high anthocyanin content are more nutritious than white tuber. But, the molecular mechanism underlying it is unknown.

RESULTS

In the current study, high-throughput RNA-sequencing was used to compare the transcriptomes between plants with tubers with red or white epidermis. Compared with the white-skinned tubers of cultivar QY3, anthocyanin biosynthesis structural genes had greater expression in the red-skinned tubers of cultivar QY1, indicating that the anthocyanin biosynthesis pathway was activated in 'QY1'; quantitative PCR confirmed this difference in expression. HtMYB2 (Unigene44371_All) was the only MYB transcription factor, homologous to the MYB transcription factor regulating anthocyanin biosynthesis, expressed in the red tuber epidermis of 'QY1'. The anthocyanin concentration in the root, stem, leaf, flower, and tuber epidermis of 'QY1' was higher than in 'QY3', especially tuber epidermis. Correspondingly, HtMYB2 had greater expression in these tissues of 'QY1' than in 'QY3'. The expression of HtMYB2 was associated with anthocyanin accumulation in the different tissues. Overexpression of HtMYB2 activated the anthocyanin biosynthesis pathway, accumulating the pigment in leaves of transgenic tobacco, supporting the model that HtMYB2 regulated anthocyanin biosynthesis. Further experiments found that HtMYB2 had the same coding sequence and genomic sequence in 'QY1' and 'QY3', but that there were several single nucleotide polymorphisms and one insertion-deletion (indel) mutation of 21 nucleotides in the promoter region between the two alleles. The deletion of three nucleotides "AAA" made the promoter of 'QY1' predicted to contain one more possible promoter region. A specific primer, based on the indel, could differentiate between cultivars with red or white tuber epidermis. The genetic variation in HtMYB2 was associated with the tuber skin color in a natural population.

CONCLUSIONS

RNA-seq can successfully isolate the candidate gene (HTMYB2) controlling anthocyanin biosynthesis in purple epidermis of Jerusalem artichoke tuber. HTMYB2 can regulate anthocyanin biosynthesis in plants and is closely related to the formation of purple phenotype in tubers. This study should be useful in understanding the genetic mechanism underlying different tuber skin colors and in breeding new H. tuberosus cultivars with different tuber skin colors.

摘要

背景

块茎颜色是菊芋(洋姜)的一个重要特征。通常,含高花青素的紫色块茎比白色块茎更有营养。但是,其背后的分子机制尚不清楚。

结果

在本研究中,使用高通量 RNA 测序比较了表皮为红色或白色的块茎植物之间的转录组。与品种 QY3 的白皮块茎相比,品种 QY1 的红皮块茎中花色苷生物合成结构基因的表达更大,表明花色苷生物合成途径在“QY1”中被激活;定量 PCR 证实了这种表达差异。HtMYB2(Unigene44371_All)是唯一的 MYB 转录因子,与调控花色苷生物合成的 MYB 转录因子同源,在“QY1”的红皮块茎表皮中表达。“QY1”的根、茎、叶、花和块茎表皮中的花色苷浓度均高于“QY3”,尤其是块茎表皮。相应地,“QY1”中这些组织的 HtMYB2 表达高于“QY3”。HtMYB2 的表达与不同组织中的花色苷积累有关。HtMYB2 的过表达激活了花色苷生物合成途径,在转基因烟草叶片中积累色素,支持 HtMYB2 调节花色苷生物合成的模型。进一步的实验发现,“QY1”和“QY3”中的 HtMYB2 具有相同的编码序列和基因组序列,但在两个等位基因之间的启动子区域存在几个单核苷酸多态性和一个 21 个核苷酸的插入缺失(indel)突变。三个核苷酸“AAA”的缺失使“QY1”的启动子预测含有一个额外的可能启动子区域。基于插入缺失的特定引物可区分表皮为红色或白色的品种。自然群体中 HtMYB2 的遗传变异与块茎皮色有关。

结论

RNA-seq 可以成功分离控制菊芋块茎紫色表皮花色苷生物合成的候选基因(HTMYB2)。HTMYB2 可以调节植物中的花色苷生物合成,与块茎中紫色表型的形成密切相关。本研究有助于了解不同块茎皮色的遗传机制,并培育具有不同块茎皮色的新型菊芋品种。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验