1995
DOI: 10.1105/tpc.7.10.1569
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A novel class of MADS box genes is involved in ovule development in petunia.

Abstract: We isolated and characterized two ovule-specific MADS box cDNAs from petunia, designated floral binding protein (fbp) genes 7 and 11. The putative protein products of these genes have -90% of their overall amino acid sequence in common. In situ RNA hybridization experiments revealed that both genes are expressed in the center of the developing gynoecium before ovule primordia are visible. At later developmental stages, hybridization signals were observed only in the ovules, suggesting that these genes are invo… Show more

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Cited by 263 publications
(113 citation statements)
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“…Moreover, studies on gene expression patterns in flowers of model plants including Arabidopsis , Petunia , and Oryza also indicate that STK, FBP7, FBP11, AGL11, and OsMADS13 are restricted to placenta/ovules (Angenent et al, 1995; Rounsley et al, 1995; Pinyopich et al, 2003; Dreni et al, 2007; Yoo et al, 2010; Li et al, 2011), while DL, CRC, and YABBY only to ovary wall (Yamaguchi et al, 2004; Dreni et al, 2007; Li et al, 2011). This implies that placenta is a distinct floral organ equivalent to a secondary shoot and independent of carpel and it is recruited onto ovary wall later in angiosperms (Angenent et al, 1995; Roe et al, 1997; Skinner et al, 2004). These conclusions are plausible considering that ovules are borne on fertile shoots in gymnosperms that have no carpels (Bierhorst, 1971; Biswas and Johri, 1997), and that ovule formation has nothing to do with carpels in mutant angiosperm (Lersten and Don, 1966; Dave et al, 1981; Skinner et al, 2004).…”
Section: Discussionmentioning
confidence: 99%
“…Moreover, studies on gene expression patterns in flowers of model plants including Arabidopsis , Petunia , and Oryza also indicate that STK, FBP7, FBP11, AGL11, and OsMADS13 are restricted to placenta/ovules (Angenent et al, 1995; Rounsley et al, 1995; Pinyopich et al, 2003; Dreni et al, 2007; Yoo et al, 2010; Li et al, 2011), while DL, CRC, and YABBY only to ovary wall (Yamaguchi et al, 2004; Dreni et al, 2007; Li et al, 2011). This implies that placenta is a distinct floral organ equivalent to a secondary shoot and independent of carpel and it is recruited onto ovary wall later in angiosperms (Angenent et al, 1995; Roe et al, 1997; Skinner et al, 2004). These conclusions are plausible considering that ovules are borne on fertile shoots in gymnosperms that have no carpels (Bierhorst, 1971; Biswas and Johri, 1997), and that ovule formation has nothing to do with carpels in mutant angiosperm (Lersten and Don, 1966; Dave et al, 1981; Skinner et al, 2004).…”
Section: Discussionmentioning
confidence: 99%
“…OMADS4 is specifically expressed only in stamens and carpels, thus resembling the expression patterns of other class C genes [111, 115, 116]. OMADS2 is only expressed in carpels, in accordance with other class D genes [117, 118]. Despite the sequence similarity, the expression patterns of OMADS4 and OMADS2 are quite divergent when compared with those of PhalAG1 and PhalAG2 and may reflect a functional evolutionary divergence of the class C/D genes in Oncidium and Phalaenopsis , with a more redundant role in the latter species than in Oncidium [95].…”
Section: The Orchid Class C and D Mads-box Genesmentioning
confidence: 99%
“…In plants, one of the most significant features of the MADS-box gene family is its essential role in the ABCDE model of flowering [2]. Numerous studies have identified its vital function in the formation and growth of floral organs [3], anthesis time [4], ovule development [5] and the ripening of fruits and seeds [6]. MADS-box gene family members have also been reported to be involved in stress responses [7], including abiotic and biotic responses [8].…”
Section: Introductionmentioning
confidence: 99%