1999
DOI: 10.1242/dev.126.12.2715
|View full text |Cite
|
Sign up to set email alerts
|

The Arabidopsis FILAMENTOUS FLOWER gene is required for flower formation

Abstract: A screen for mutations affecting flower formation was carried out and several filamentous flower (fil) alleles were identified. In fil mutants, floral primordia occasionally give rise to pedicels lacking flowers at their ends. This defect is dramatically enhanced in fil rev double mutants, in which every floral primordium produces a flowerless pedicel. These data suggest that the FIL and REV genes are required for an early step of flower formation, possibly for the establishment of a flower-forming domain with… Show more

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
3
1
1

Citation Types

0
17
0
1

Year Published

2001
2001
2022
2022

Publication Types

Select...
5
3

Relationship

0
8

Authors

Journals

citations
Cited by 124 publications
(18 citation statements)
references
References 27 publications
0
17
0
1
Order By: Relevance
“…These YABBY genes were initially and extensively studied in Arabidopsis, and they were shown to play important roles in the specification of abaxial cell fates in lateral organs produced by apical and flower meristems in both distinct and redundant manners [8]. FIL is required for the normal formation and development of inflorescence and floral meristems; its mutation (fil) generates clusters of both filamentous structures and flowers with floral organs of altered number and shape [7,9,[13][14][15]. The fil yab3 double mutant showed obvious changes in vegetative phenotypes (such as cotyledons and leaves with linear forms, abnormal vasculature and leaf surface with abaxial character, and ectopic shoot apical meristem structures) and displayed severely radialized floral organs [6].…”
Section: Introductionmentioning
confidence: 99%
“…These YABBY genes were initially and extensively studied in Arabidopsis, and they were shown to play important roles in the specification of abaxial cell fates in lateral organs produced by apical and flower meristems in both distinct and redundant manners [8]. FIL is required for the normal formation and development of inflorescence and floral meristems; its mutation (fil) generates clusters of both filamentous structures and flowers with floral organs of altered number and shape [7,9,[13][14][15]. The fil yab3 double mutant showed obvious changes in vegetative phenotypes (such as cotyledons and leaves with linear forms, abnormal vasculature and leaf surface with abaxial character, and ectopic shoot apical meristem structures) and displayed severely radialized floral organs [6].…”
Section: Introductionmentioning
confidence: 99%
“…Grapevine VviFAS was found to share a collinearity relationship with tomato FAS genes, suggesting that they probably possess similar functions. (Chen et al, 1999;Monforte et al, 2014). The expression pattern of AtCRC was mostly restricted to carpels and nectaries, while CRC plays a critical role in carpel morphogenesis, floral determinacy, and nectary specification in Arabidopsis (Bowman and Smyth, 1999).…”
Section: Discussion Evolution and Structure Of The Vviyabs Family In ...mentioning
confidence: 99%
“…Among them, FIL, YAB2, YAB3, and YAB5 function redundantly to control the development of lateral organs (Siegfried et al, 1999;Yamada et al, 2011;Yang et al, 2018). In Arabidopsis, FIL is responsible for the flower formation and development (Chen et al, 1999;Sawa et al, 1999a, Sawa et al, 1999b. Similarly, the TOB1-related YAB genes in rice have conserved functions in flower development (Tanaka et al, 2017).…”
Section: Introductionmentioning
confidence: 99%
“…There were 509 cis-elements in 92 categories in the promoter of BpYAB3, of which the most numerous ones were DOFCOREZM (39), ROOTMOTIFTAPOX1 (33), CACTFTPPCA1 (30), CAATBOX1 (28), ARR1AT (20), GATABOX (18), MARTBOX (18), GT1CONSENSUS (17), etc. There were 469 cis-elements in 102 categories in the promoter of BpYAB4, of which the most numerous ones were GT1CONSENSUS (28), CACTFTPPCA1 (26), ARR1AT (25), CAATBOX1 (25), DOFCOREZM (24), ROOTMOTIFTAPOX1 (17), GTGANTG10 (16), GATABOX (15), etc. In the promoter of BpYAB5, there were 470 cis-elements in 94 categories, among which there were DOFCOREZM (48), POLLEN1LELAT52 (28), GT1CONSENSUS (23), ARR1AT (21), CAATBOX1 (19), CACTFTPPCA1 (19), ROOTMOTIFTAPOX1 (16), GATABOX (15), and so on.…”
Section: Analysis Of Cis-acting Elements In the Promoters Of Bpyab Genesmentioning
confidence: 99%
“…The CRC gene is essential for carpel polarity establishment and nectary specification in A. thaliana [14], while INO expresses in the outermost cell layer of the ovule and promotes outer integument growth [15]. The other four AtYAB genes have redundant functions in repressing the shoot apical meristem (SAM) and activating laminar development [16,17]; thus, YABBY is considered to be the candidate gene for the evolution of stem-to-leaf transformation [18]. Ectopic SAM and axillary meristems are formed in the fil yab3 mutant, and the stem cell activity-associated gene CLAVATA3 (CLV3) and WUSCHEL (WUS) are expanded in the fil yab3 double mutant [19].…”
Section: Introductionmentioning
confidence: 99%