Department of Electrical Engineering, I-Shou University, Kaohsiung, Taiwan.
The School of Chinese Medicine for Post-Baccalaureate, I-Shou University, Kaohsiung, Taiwan.
Biol Res. 2019 Apr 24;52(1):25. doi: 10.1186/s40659-019-0233-8.
The morphological diversity of flower organs is closely related to functional divergence within the MADS-box gene family. Bryophytes and seedless vascular plants have MADS-box genes but do not have ABCDE or AGAMOUS-LIKE6 (AGL6) genes. ABCDE and AGL6 genes belong to the subgroup of MADS-box genes. Previous works suggest that the B gene was the first ABCDE and AGL6 genes to emerge in plant but there are no mentions about the probable origin time of ACDE and AGL6 genes. Here, we collected ABCDE and AGL6 gene 381 protein sequences and 361 coding sequences from gymnosperms and angiosperms and reconstructed a complete Bayesian phylogeny of these genes. In this study, we want to clarify the probable origin time of ABCDE and AGL6 genes is a great help for understanding the role of the formation of the flower, which can decipher the forming order of MADS-box genes in the future.
These genes appeared to have been under purifying selection and their evolutionary rates are not significantly different from each other. Using the Bayesian evolutionary analysis by sampling trees (BEAST) tool, we estimated that: the mutation rate of the ABCDE and AGL6 genes was 2.617 × 10 substitutions/site/million years, and that B genes originated 339 million years ago (MYA), CD genes originated 322 MYA, and A genes shared the most recent common ancestor with E/AGL6 296 MYA, respectively.
The phylogeny of ABCDE and AGL6 genes subfamilies differed. The APETALA1 (AP1 or A gene) subfamily clustered into one group. The APETALA3/PISTILLATA (AP3/PI or B genes) subfamily clustered into two groups: the AP3 and PI clades. The AGAMOUS/SHATTERPROOF/SEEDSTICK (AG/SHP/STK or CD genes) subfamily clustered into a single group. The SEPALLATA (SEP or E gene) subfamily in angiosperms clustered into two groups: the SEP1/2/4 and SEP3 clades. The AGL6 subfamily clustered into a single group. Moreover, ABCDE and AGL6 genes appeared in the following order: AP3/PI → AG/SHP/STK → AGL6/SEP/AP1. In this study, we collected candidate sequences from gymnosperms and angiosperms. This study highlights important events in the evolutionary history of the ABCDE and AGL6 gene families and clarifies their evolutionary path.
花器官的形态多样性与 MADS 框基因家族的功能分化密切相关。苔藓植物和无种子维管植物具有 MADS 框基因,但没有 ABCDE 或 AGAMOUS-LIKE6(AGL6)基因。ABCDE 和 AGL6 基因属于 MADS 框基因的亚组。先前的研究表明,B 基因是植物中最早出现的 ABCDE 和 AGL6 基因,但没有提到 ACDE 和 AGL6 基因的可能起源时间。在这里,我们从裸子植物和被子植物中收集了 381 个 ABCDE 和 AGL6 基因的蛋白质序列和 361 个编码序列,并重建了这些基因的完整贝叶斯系统发育。在这项研究中,我们希望澄清 ABCDE 和 AGL6 基因的可能起源时间对理解花的形成有很大帮助,这有助于我们在未来破译 MADS 框基因的形成顺序。
这些基因似乎受到了纯化选择的影响,它们的进化速率彼此之间没有显著差异。使用贝叶斯进化分析采样树(BEAST)工具,我们估计:ABCDE 和 AGL6 基因的突变率为 2.617×10 个替换/位点/百万年,B 基因起源于 3.39 亿年前(MYA),CD 基因起源于 3.22 MYA,A 基因与 E/AGL6 的最近共同祖先可追溯到 2.96 MYA。
ABCDE 和 AGL6 基因亚家族的系统发育不同。APETALA1(AP1 或 A 基因)亚家族聚为一组。APETALA3/PISTILLATA(AP3/PI 或 B 基因)亚家族聚为两组:AP3 和 PI 分支。AGAMOUS/SHATTERPROOF/SEEDSTICK(AG/SHP/STK 或 CD 基因)亚家族聚为一组。被子植物的 SEPALLATA(SEP 或 E 基因)亚家族聚为两组:SEP1/2/4 和 SEP3 分支。AGL6 亚家族聚为一组。此外,ABCDE 和 AGL6 基因的出现顺序为:AP3/PI→AG/SHP/STK→AGL6/SEP/AP1。在本研究中,我们从裸子植物和被子植物中收集了候选序列。本研究强调了 ABCDE 和 AGL6 基因家族进化历史中的重要事件,并阐明了它们的进化途径。