Functional conservation and divergence of five SEPALLATA-like genes from a basal eudicot tree, Platanus acerifolia

被引:27
作者
Zhang, Sisi [1 ]
Lu, Shunjiao [1 ,2 ]
Yi, Shuangshuang [1 ,2 ]
Han, Hongji [1 ]
Liu, Lei [1 ]
Zhang, Jiaqi [1 ]
Bao, Manzhu [1 ]
Liu, Guofeng [1 ]
机构
[1] Huazhong Agr Univ, Coll Hort & Forestry Sci, Key Lab Hort Plant Biol, Minist Educ, Wuhan 430070, Peoples R China
[2] Chinese Acad Trop Agr Sci CATAS, Trop Crops Genet Resources Inst, Key Lab Crop Gene Resources & Germplasm Enhanceme, Minist Agr, Danzhou 571737, Peoples R China
基金
中国国家自然科学基金;
关键词
Floral development; Landscape plant; London plane; MADS-box; Protein-protein interaction; SEP; MADS-BOX GENES; FLORAL HOMEOTIC GENES; ORGAN IDENTITY; FLOWER DEVELOPMENT; EXPRESSION; FRUIT; DIVERSIFICATION; PROTEINS; EVOLUTION; INFLORESCENCE;
D O I
10.1007/s00425-016-2617-0
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
Five SEP -like genes were cloned and identified from Platanus acerifolia through the analysis of expression profiles, protein-protein interaction patterns, and transgenic phenotypes, which suggested that they play conservative and diverse functions in floral initiation and development, fruit development, bud growth, and dormancy. SEPALLATA (SEP) genes have been well characterized in core eudicots and some monocots, and they play important and diverse roles in plant development, including flower meristem initiation, floral organ identity, and fruit development and ripening. However, the knowledge on the function and evolution of SEP-like genes in basal eudicot species is very limited. Here, we cloned and identified five SEP-like genes from London plane (Platanus acerifolia), a basal eudicot tree that is widely used for landscaping in cities. Sequence alignment and phylogenetic analysis indicated that three genes (PlacSEP1.1, PlacSEP1.2, and PlacSEP1.3) belong to the SEP1/2/4 clade, while the other two genes (PlacSEP3.1 and PlacSEP3.2) are grouped into the SEP3 clade. Quantitative real-time PCR (qRT-PCR) analysis showed that all PlacSEPs, except PlacSEP1.1 and PlacSEP1.2, were expressed during the male and female inflorescence initiation, and throughout the flower and fruit development process. PlacSEP1.2 gene expression was only detected clearly in female inflorescence at April. PlacSEP1.3 and PlacSEP3.1 were also expressed, although relatively weak, in vegetative buds of adult trees. No evident PlacSEPs transcripts were detected in various organs of juvenile trees. Overexpression of PlacSEPs in Arabidopsis and tobacco plants resulted in different phenotypic alterations. 35S:PlacSEP1.1, 35S:PlacSEP1.3, and 35S:PlacSEP3.2 transgenic Arabidopsis plants showed evident early flowering, with less rosette leaves but more cauline leaves, while 35S:PlacSEP1.2 and PlacSEP3.1 transgenic plants showed no visible phenotypic changes. 35S:PlacSEP1.1 and 35S:PlacSEP3.2 transgenic Arabidopsis plants also produced smaller and curled leaves. Overexpression of PlacSEP1.1 and PlacSEP3.1 in tobacco resulted in the early flowering and producing more lateral branches. Yeast two-hybrid analysis indicated that PlacSEPs proteins can form homo- or hetero-dimers with the Platanus APETALA1 (AP1)/FRUITFULL (FUL), B-, C-, and D-class MADS-box proteins in different interacting patterns and intensities. Our results suggest that the five PlacSEP genes may play important and divergent roles during floral initiation and development, as well as fruit development, by collaborating with FUL, B-, C-, and D-class MADS-box genes in London plane; PlacSEP1.3 and PlacSEP3.1 genes might also involve in vegetative bud growth and dormancy. The results provide valuable data for us to understand the functional evolution of SEP-like genes in basal eudicot species.
引用
收藏
页码:439 / 457
页数:19
相关论文
共 65 条
  • [1] Down-regulation of TM29, a tomato SEPALLATA homolog, causes parthenocarpic fruit development and floral reversion
    Ampomah-Dwamena, C
    Morris, BA
    Sutherland, P
    Veit, B
    Yao, JL
    [J]. PLANT PHYSIOLOGY, 2002, 130 (02) : 605 - 617
  • [2] A NOVEL CLASS OF MADS BOX GENES IS INVOLVED IN OVULE DEVELOPMENT IN PETUNIA
    ANGENENT, GC
    FRANKEN, J
    BUSSCHER, M
    VANDIJKEN, A
    VANWENT, JL
    DONS, HJM
    VANTUNEN, AJ
    [J]. PLANT CELL, 1995, 7 (10) : 1569 - 1582
  • [3] BOWMAN JL, 1991, DEVELOPMENT, V112, P1
  • [4] Byng JW, 2016, BOT J LINN SOC, V181, P1, DOI [10.1111/boj.12385, 10.1111/j.1095-8339.2009.00996.x]
  • [5] A new role of the Arabidopsis SEPALLATA3 gene revealed by its constitutive expression
    Castillejo, C
    Romera-Branchat, M
    Pelaz, S
    [J]. PLANT JOURNAL, 2005, 43 (04) : 586 - 596
  • [6] Floral organ identity: 20 years of ABCs
    Causier, Barry
    Schwarz-Sommer, Zsuzsanna
    Davies, Brendan
    [J]. SEMINARS IN CELL & DEVELOPMENTAL BIOLOGY, 2010, 21 (01) : 73 - 79
  • [7] Four Orchid (Oncidium Gower Ramsey) AP1/AGL9-like MADS Box Genes Show Novel Expression Patterns and Cause Different Effects on Floral Transition and Formation in Arabidopsis thaliana
    Chang, Yu-Yun
    Chiu, Yi-Feng
    Wu, Jia-Wei
    Yang, Chang-Hsien
    [J]. PLANT AND CELL PHYSIOLOGY, 2009, 50 (08) : 1425 - 1438
  • [8] Floral dip:: a simplified method for Agrobacterium-mediated transformation of Arabidopsis thaliana
    Clough, SJ
    Bent, AF
    [J]. PLANT JOURNAL, 1998, 16 (06) : 735 - 743
  • [9] THE WAR OF THE WHORLS - GENETIC INTERACTIONS CONTROLLING FLOWER DEVELOPMENT
    COEN, ES
    MEYEROWITZ, EM
    [J]. NATURE, 1991, 353 (6339) : 31 - 37
  • [10] SEP-class genes in Populus tremuloides and their likely role in reproductive survival of poplar trees
    Cseke, LJ
    Cseke, SB
    Ravinder, N
    Taylor, LC
    Shankar, A
    Sen, B
    Thakur, R
    Karnosky, DF
    Podila, GK
    [J]. GENE, 2005, 358 : 1 - 16