scholarly journals The Roles of Floral Organ Genes in Regulating Rosaceae Fruit Development

2022 ◽  
Vol 12 ◽  
Author(s):  
Jia-Long Yao ◽  
Chunying Kang ◽  
Chao Gu ◽  
Andrew Peter Gleave

The function of floral organ identity genes, APETALA1/2/3, PISTILLATA, AGAMOUS, and SEPALLATA1/2/3, in flower development is highly conserved across angiosperms. Emerging evidence shows that these genes also play important roles in the development of the fruit that originates from floral organs following pollination and fertilization. However, their roles in fruit development may vary significantly between species depending on the floral organ types contributing to the fruit tissues. Fruits of the Rosaceae family develop from different floral organ types depending on the species, for example, peach fruit flesh develops from carpellary tissues, whereas apple and strawberry fruit flesh develop from extra-carpellary tissues, the hypanthium and receptacle, respectively. In this review, we summarize recent advances in understanding floral organ gene function in Rosaceae fruit development and analyze the similarities and diversities within this family as well as between Rosaceae and the model plant species Arabidopsis and tomato. We conclude by suggesting future research opportunities using genomics resources to rapidly dissect gene function in this family of perennial plants.

Genetics ◽  
2002 ◽  
Vol 160 (4) ◽  
pp. 1641-1650 ◽  
Author(s):  
Kenneth M Olsen ◽  
Andrew Womack ◽  
Ashley R Garrett ◽  
Jane I Suddith ◽  
Michael D Purugganan

AbstractThe floral developmental pathway in Arabidopsis thaliana is composed of several interacting regulatory genes, including the inflorescence architecture gene TERMINAL FLOWER1 (TFL1), the floral meristem identity genes LEAFY (LFY), APETALA1 (AP1), and CAULIFLOWER (CAL), and the floral organ identity genes APETALA3 (AP3) and PISTILLATA (PI). Molecular population genetic analyses of these different genes indicate that the coding regions of AP3 and PI, as well as AP1 and CAL, share similar levels and patterns of nucleotide diversity. In contrast, the coding regions of TFL1 and LFY display a significant reduction in nucleotide variation, suggesting that these sequences have been subjected to a recent adaptive sweep. Moreover, the promoter of TFL1, unlike its coding region, displays high levels of diversity organized into two distinct haplogroups that appear to be maintained by selection. These results suggest that patterns of molecular evoution differ among regulatory genes in this developmental pathway, with the earlier acting genes exhibiting evidence of adaptive evolution.


2011 ◽  
Vol 24 (12) ◽  
pp. 1502-1512 ◽  
Author(s):  
Yi-Ting Su ◽  
Jen-Chih Chen ◽  
Chan-Pin Lin

Floral symptoms caused by phytoplasma largely resemble floral reversion in other plants. Periwinkle leaf yellowing (PLY) phytoplasma and peanut witches'-broom (PnWB) phytoplasma caused different degrees of floral abnormalities on infected periwinkle plants. The PLY phytoplasma-infected plants exhibited floral discoloration, virescence, small flowers, and only occasionally full floral reversion. In contrast, PnWB phytoplasma frequently induced complete floral reversion and resulted in a witches'-broom symptom from the floral reversion. Although different degrees of floral symptoms were induced by these two phytoplasmas, the morphological disorders were similar to those of other plants carrying SEPALLATA mutations or gene silencing. Here, we compared expression levels of organ-identity-related genes and pigmentation genes during floral symptom development. Accumulation of phytoplasmas in malformed flowers and their closely surrounding leaves was also compared. In infected plants, transcript abundance of all examined organ identity genes and pigmentation genes was suppressed. Indeed, CrSEP3, a SEPALLALA3 ortholog, showed the greatest suppression among genes examined. Of the pigmentation genes, transcript reduction of chalcone synthase was most highly correlated with the loss in floral pigmentation. Floral symptom severities were associated with the accumulation of either phytoplasmas. Interestingly, both phytoplasmas accumulated to higher levels in malformed flowers than in their surrounding leaves. Many plant pathogens manipulate host plant development to their advantage. It is intriguing to see whether phytoplasmas alter floral development to increase their population.


2022 ◽  
Author(s):  
Jing You ◽  
Qiannan Duan ◽  
Jun Zhang ◽  
Wenqiang Shen ◽  
Yue Zhou ◽  
...  

Abstract The lemma and palea are floral organ structures unique to grasses, and their development affects grain size. However, information on the molecular mechanism of lemma development is limited. In this study, we investigated a rice spikelet mutant, degenerated lemma (del), which developed florets with a slightly degenerated or rod-like lemma. The results indicate that the mutation of the DEL gene interfered with lemma development. In addition, del also showed a significant reduction in grain length and width, seed setting rate, and 1000-grain weight, which led to a reduction in yield. The results indicate that the mutation of the DEL gene further affects rice grain yield. Map-based cloning shows a single-nucleotide substitution from T to A within Os01g0527600/DEL, causing an amino acid mutation of Leu-34 to His-34 in the del mutant. DEL is an allele of OsRDR6, encoding the RNA-dependent RNA polymerase 6, and is highly expressed in the spikelet. RT-qPCR results show that the expression of some floral organ identity genes was changed, which indicates that the DEL gene regulates lemma development by modulating the expression of these genes. The present results suggest that DEL plays an important role in lemma development and rice grain yield.


Development ◽  
1996 ◽  
Vol 122 (4) ◽  
pp. 1261-1269 ◽  
Author(s):  
M.P. Running ◽  
E.M. Meyerowitz

An open question in developmental biology is how groups of dividing cells can generate specific numbers of segments or organs. We describe the phenotypic effects of mutations in PERIANTHIA, a gene specifically required for floral organ patterning in Arabidopsis thaliana. Most wild-type Arabidopsis flowers have 4 sepals, 4 petals, 6 stamens, and 2 carpels. Flowers of perianthia mutant plants most commonly show a pentamerous pattern of 5 sepals, 5 petals 5 stamens, and 2 carpels. This pattern is characteristic of flowers in a number of plant families, but not in the family Brassicaceae, which includes Arabidopsis. Unlike previously described mutations affecting floral organ number, perianthia does not appear to affect apical or floral meristem sizes, nor is any other aspect of vegetative or floral development severely affected. Floral organs in perianthia arise in a regular, stereotypical pattern similar to that in distantly related species with pentamerous flowers. Genetic analysis shows that PERIANTHIA acts downstream of the floral meristem identity genes and independently of the floral meristem size and floral organ identity genes in establishing floral organ initiation patterns. Thus PERIANTHIA acts in a previously unidentified process required for organ patterning in Arabidopsis flowers.


1997 ◽  
Vol 9 (4) ◽  
pp. 559-570 ◽  
Author(s):  
A Samach ◽  
S E Kohalmi ◽  
P Motte ◽  
R Datla ◽  
G W Haughn

1997 ◽  
Vol 9 (4) ◽  
pp. 559
Author(s):  
Alon Samach ◽  
Susanne E. Kohalmi ◽  
Patrick Motte ◽  
Raju Datla ◽  
George W. Haughn

2006 ◽  
Vol 46 (1) ◽  
pp. 54-68 ◽  
Author(s):  
Yifeng Xu ◽  
Lai Lai Teo ◽  
Jing Zhou ◽  
Prakash P. Kumar ◽  
Hao Yu

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