College of Agronomy, Northwest A&F University, Yangling, 712100, Shaanxi, China.
School of Stomatology, Wuhan University, Wuhan, 430072, Hubei, China.
BMC Genomics. 2018 Oct 3;19(1):726. doi: 10.1186/s12864-018-5113-z.
MADS-box genes encode transcription factors that are known to be involved in several aspects of plant growth and development, especially in floral organ specification. To date, the comprehensive analysis of potato MADS-box gene family is still lacking after the completion of potato genome sequencing. A genome-wide characterization, classification, and expression analysis of MADS-box transcription factor gene family was performed in this study.
A total of 153 MADS-box genes were identified and categorized into MIKC subfamily (MIKC and MIKC) and M-type subfamily (Mα, Mβ, and Mγ) based on their phylogenetic relationships to the Arabidopsis and rice MADS-box genes. The potato M-type subfamily had 114 members, which is almost three times of the MIKC members (39), indicating that M-type MADS-box genes have a higher duplication rate and/or a lower loss rate during potato genome evolution. Potato MADS-box genes were present on all 12 potato chromosomes with substantial clustering that mainly contributed by the M-type members. Chromosomal localization of potato MADS-box genes revealed that MADS-box genes, mostly MIKC, were located on the duplicated segments of the potato genome whereas tandem duplications mainly contributed to the M-type gene expansion. The potato MIKC subfamily could be further classified into 11 subgroups and the TT16-like, AGL17-like, and FLC-like subgroups found in Arabidopsis were absent in potato. Moreover, the expressions of potato MADS-box genes in various tissues were analyzed by using RNA-seq data and verified by quantitative real-time PCR, revealing that the MIKC genes were mainly expressed in flower organs and several of them were highly expressed in stolon and tubers. StMADS1 and StMADS13 were up-regulated in the StSP6A-overexpression plants and down-regulated in the StSP6A-RNAi plant, and their expression in leaves and/or young tubers were associated with high level expression of StSP6A.
Our study identifies the family members of potato MADS-box genes and investigate the evolution history and functional divergence of MADS-box gene family. Moreover, we analyze the MIKC expression patterns and screen for genes involved in tuberization. Finally, the StMADS1 and StMADS13 are most likely to be downstream target of StSP6A and involved in tuber development.
MADS-box 基因编码转录因子,已知其参与植物生长和发育的多个方面,特别是花器官的特化。迄今为止,在完成马铃薯基因组测序后,对马铃薯 MADS-box 基因家族的全面分析仍然缺乏。本研究对 MADS-box 转录因子基因家族进行了全基因组特征分析、分类和表达分析。
共鉴定出 153 个 MADS-box 基因,并根据与拟南芥和水稻 MADS-box 基因的系统发育关系,将其分为 MIKC 亚家族(MIKC 和 MIKC)和 M 型亚家族(Mα、Mβ 和 Mγ)。马铃薯 M 型亚家族有 114 个成员,几乎是 MIKC 成员(39 个)的三倍,表明 M 型 MADS-box 基因在马铃薯基因组进化过程中具有更高的复制率和/或更低的丢失率。马铃薯 MADS-box 基因存在于马铃薯的 12 条染色体上,主要由 M 型成员聚类。马铃薯 MADS-box 基因的染色体定位表明,MADS-box 基因,主要是 MIKC,位于马铃薯基因组的重复片段上,而串联重复主要导致 M 型基因的扩张。马铃薯 MIKC 亚家族可进一步分为 11 个亚群,在拟南芥中发现的 TT16 样、AGL17 样和 FLC 样亚群在马铃薯中不存在。此外,通过 RNA-seq 数据和定量实时 PCR 验证分析了马铃薯 MADS-box 基因在各种组织中的表达情况,结果表明 MIKC 基因主要在花器官中表达,其中一些在匍匐茎和块茎中高表达。StMADS1 和 StMADS13 在 StSP6A 过表达植株中上调,在 StSP6A-RNAi 植株中下调,它们在叶片和/或幼块茎中的表达与 StSP6A 的高水平表达相关。
本研究鉴定了马铃薯 MADS-box 基因的家族成员,并研究了 MADS-box 基因家族的进化历史和功能分化。此外,我们分析了 MIKC 的表达模式,并筛选了与块茎形成有关的基因。最后,StMADS1 和 StMADS13 很可能是 StSP6A 的下游靶标,并参与块茎发育。