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Volumn 5, Issue 5, 1995, Pages 628-639

MADS-box genes in plant ontogeny and phylogeny: Haeckel's 'biogenetic law' revisited

Author keywords

[No Author keywords available]

Indexed keywords

DEVELOPMENTAL GENETICS; EVOLUTION; HOMEOBOX; MULTIGENE FAMILY; ONTOGENY; PHYLOGENY; PLANT; PRIORITY JOURNAL; REVIEW;

EID: 0029113636     PISSN: 0959437X     EISSN: None     Source Type: Journal    
DOI: 10.1016/0959-437X(95)80032-8     Document Type: Article
Times cited : (127)

References (97)
  • 1
    • 0026847624 scopus 로고
    • Ontogeny and phylogeny — revisited and reunited
    • (1992) Bioessays , vol.14 , pp. 275-279
    • Gould1
  • 5
    • 0028003107 scopus 로고
    • The molecular architects of body design
    • (February)
    • (1994) Sci Am , vol.270 , pp. 36-42
    • McGinnis1    Kuziora2
  • 7
    • 0028934434 scopus 로고
    • The MADS-box family of transcription factors
    • of special interest, The most recent and comprehensive review of the MADS-box gene family.
    • (1995) Eur J Biochem , vol.229 , pp. 1-13
    • Shore1    Sharrocks2
  • 9
    • 0028917564 scopus 로고
    • Requirement of MADS domain transcription factor D-MEF2 for muscle formation in Drosophila
    • of outstanding interest, The function of the single MEF2 gene from Drosophila was determined by generating a loss-of-function mutant. In mutant embryos, somatic, cardiac and visceral muscle cells did not differentiate, but myoblasts were normally specified. This demonstrates that different muscle cell types share a common myogenic differentiation program controlled by MEF2. Though it is known even to us that flies are not plants, these results are mentioned in this review because they illustrate beautifully that the ‘synteny of functions’ is not restricted to the plant lineage. Although insects and vertebrates separated 〉500 million years ago, they still share structurally and functionally highly related MEF2-type MADS-box genes, with the remarkable difference that mammals have at least four genes, whereas Drosophila has just one, which is reminiscent of the four clusters of mammalian Hox genes in contrast to the single cluster of insects.
    • (1995) Science , vol.267 , pp. 688-693
    • Lilly1    Zhao2    Ranganayakulu3    Paterson4    Schulz5    Olson6
  • 11
    • 0026417225 scopus 로고
    • The war of the whorls: genetic interactions controlling flower development
    • (1991) Nature , vol.353 , pp. 31-37
    • Coen1    Meyerowitz2
  • 13
    • 12044252185 scopus 로고
    • The unfolding drama of flower development: recent results from genetic and molecular analyses
    • (1994) Genes Dev , vol.8 , pp. 745-756
    • Ma1
  • 14
    • 0027768566 scopus 로고
    • Molecular biology of flower development in Antirrhinum majus (snapdragon)
    • (1993) Gene , vol.135 , pp. 239-243
    • Saedler1    Huijser2
  • 15
    • 0028711166 scopus 로고
    • Genetic analyses of signalling in flower development using Arabidopsis
    • (1994) Plant Mol Biol , vol.26 , pp. 1357-1377
    • Okada1    Shimura2
  • 17
    • 0002834884 scopus 로고
    • The Genetics of Flower Development
    • of special interest, Could be read as a ‘MADS-box genes for beginners’ article and as a first introduction to the complex genetics of flower development.
    • (1994) Scientific American , vol.271 , pp. 40-47
    • Meyerowitz1
  • 18
    • 0028142020 scopus 로고
    • The ABCs of floral homeotic genes
    • of special interest, Describes the ABC model of homeotic flower organ—identity gene function.
    • (1994) Cell , vol.78 , pp. 203-209
    • Weigel1    Meyerowitz2
  • 19
    • 0000007393 scopus 로고
    • On the life strategies of plants and animals
    • (1985) Trends Genet , vol.1 , pp. 165-169
    • Walbot1
  • 20
    • 0027471974 scopus 로고
    • Complementary floral homeotic phenotypes result from opposite orientations of a transposon at the plena locus of Antirrhinum
    • (1993) Cell , vol.72 , pp. 85-95
    • Bradley1    Carpenter2    Sommer3    Hartley4    Coen5
  • 23
    • 0028346564 scopus 로고
    • Ectopic expression of a single homeotic gene, the Petunia gene green petal, is sufficient to convert sepals to petaloid organs
    • (1994) EMBO J , vol.13 , pp. 1443-1449
    • Halfter1    Ali2    Stockhaus3    Ren4    Chua5
  • 24
    • 0028273861 scopus 로고
    • Arabidopsis homeotic gene APETALA3 ectopic expression: transcriptional and posttranscriptional regulation determine floral organ identity
    • (1994) Cell , vol.76 , pp. 703-716
    • Jack1    Fox2    Meyerowitz3
  • 29
    • 0027689302 scopus 로고
    • Molecular cloning and expression patterns of three alleles of the Deficiens-homologous gene St-Deficiens from Solanum tuberosum
    • (1993) Plant J , vol.4 , pp. 771-780
    • Garcia-Maroto1    Salamini2    Rohde3
  • 30
    • 0027316184 scopus 로고
    • NTGLO: a tobacco homologue of the GLOBOSA floral homeotic gene of Antirrhinum majus: cDNA sequence and expression pattern
    • (1993) Mol Gen Genet , vol.239 , pp. 310-312
    • Hansen1    Estruch2    Sommer3    Spena4
  • 31
    • 0028675707 scopus 로고
    • Comparison of MADS box gene expression in developing male and female flowers of the dioecious plant white campion
    • of special interest, From the dioecious plant Silene latifolia, the authors have isolated cDNAs of putative orthologs of MADS-box genes well characterized in the hermaphroditic model plants Antirrhinum majus and Arabidopsis thaliana and have studied the expression of these genes. Unfortunately, the authors have to conclude from their data that the studied MADS-box genes are not directly involved in sex determination in Silene. However, they do report the interesting finding that two of their genes, SLM4 and SLM5, are expressed in inflorescence meristems as well as flower meristems, whereas the presumed orthologs from Antirrhinum and Arabidopsis, SQUAMOSA and APETALA1, respectively, are not expressed in inflorescence meristems. As Silene has a determinate dichasial inflorescence, whereas Antirrhinum and Arabidopsis have an indeterminate apical inflorescence meristem, the different expression of the SQUAMOSA-like genes may reflect differences in [[Truncated]]
    • (1994) Plant Cell , vol.6 , pp. 1775-1787
    • Hardenack1    Ye2    Saedler3    Grant4
  • 32
    • 0027743044 scopus 로고
    • Conversion of perianth into reproductive organs by ectopic expression of the tobacco floral homeotic gene NAG1
    • (1993) Plant Physiol , vol.103 , pp. 1041-1046
    • Kempin1    Mandel2    Yanofsky3
  • 33
    • 0028956983 scopus 로고
    • Molecular basis of the cauliflower phenotype in Arabidopsis
    • of special interest, Isolation of the CAULIFLOWER gene from Arabidopsis thaliana reveals that it is a MADS-box gene closely related in sequence to APETALA1. Analysis of the cultivated garden variety of cauliflower (Brassica oleracea var. botrytis) showed that its putative CAULIFLOWER gene ortholog is not functional, suggesting a molecular basis for an interesting domestication process based on one of the oldest recognized flower abnormalities.
    • (1995) Science , vol.267 , pp. 522-525
    • Kempin1    Savidge2    Yanofsky3
  • 41
    • 0343558070 scopus 로고
    • Divergence in the role of MADS box genes in the determination of floral organ identity
    • (1993) Bioessays , vol.15 , pp. 691-693
    • Xue1    Ingram2
  • 43
    • 0029067947 scopus 로고
    • Chromosomal mapping of the MADS-box multigene family in Zea mays reveals dispersed distribution of allelic genes as well as transposed copies
    • of special interest, Determination of chromosomal map positions of MADs-box genes in recombinant inbred lines of maize revealed that these genes are strongly dispersed throughout the maize genome, a finding which is very likely representative of plant MADS-box genes in general. Moreover, a family of MADS-box containing elements was detected whose members resemble transposable elements in some aspects. Members of that family are present in some maize lines at certain chromosomal position, but are absent there in other lines.
    • (1995) Nucleic Acids Res , vol.23 , pp. 1901-1911
    • Fischer1    Baum2    Saedler3    Theiβen4
  • 44
    • 0029048799 scopus 로고
    • Restriction fragment length polymorphism-coupled domain-directed differential display: a highly efficient technique for expression analysis of multigene families
    • of special interest, MADS-box gene expression in the male and female inflorescences of Zea mays was used as a model system to establish an efficient technique for expression analysis of multigene families. Hopefully, the method will facilitate developmental, as well as evolutionary, studies on different gene families and in diverse organisms.
    • (1995) Proc Natl Acad Sci USA , vol.92 , pp. 5331-5335
    • Fischer1    Saedler2    Theiβen3
  • 45
    • 0027691860 scopus 로고
    • Nucleotide sequence of a flower-specific MADS box cDNA clone from orchid
    • (1993) Plant Mol Biol , vol.23 , pp. 901-904
    • Lu1    Wu2    Loh3    Yeong4    Goh5
  • 46
    • 84910881299 scopus 로고
    • “On the Origin of Species”: mythological and molecular biological ideas on the evolution of maize [in German]
    • B Parthier, Deutsche Akademie der Naturforscher Leopoldina e.V, Halle (Saale), Leopoldina (R.3)
    • (1994) Jahrbuch 1993 , vol.39 , pp. 261-275
    • Saedler1    Theiβen2
  • 49
    • 0028960139 scopus 로고
    • Structural characterization, chromosomal localization and phylogenetic evaluation of two pairs of AGAMOUS-like MADS-box genes from maize
    • of special interest, The first two genomic structures of MADS-box genes from a mono-cotyledonous plant are presented and are shown to be highly similar to some AGAMOUS-like genes from dicots. Phylogenetic evaluation of the sequences of these and the cDNAs of two other genes and chromosomal mapping both suggest that two pairs of genes have been identified that were created during duplication of chromosomal segments or complete chromosomes. These data make it seem likely that many MADS-box genes of diploid dicots are orthologous to pairs of paralogs from maize, probably because of the ‘tetraploid’ genome constitution of maize.
    • (1995) Gene , vol.156 , pp. 155-166
    • Theiβen1    Strater2    Fischer3    Saedler4
  • 51
    • 0029109360 scopus 로고
    • Conifer homologues to genes that control floral development in angiosperms
    • of outstanding interest, The first documentation of the presence of MADS-box genes (DAL1–3) in a non-flowering seed plant, a plant bearing truly unisexual axes (Norway spruce, Picea abies). According to their MADS-box sequences, these genes belong to three different subfamilies that were previously known only in angiosperms (Table 1). Tandre show that the subfamily assignment is in agreement with phylogenetic tree reconstructions and the expression patterns of the genes, which supports our notion that the membership of a MADS-box gene to a certain subfamily can be determined quite reliably from the MADS-box sequence (G Theiβen, J Kim, H Saedler, unpublished data). Furthermore, the presented data demonstrate that at least three of the MADS-box gene subfamilies of plants had already been established in the last common ancestor of conifers and angiosperms, suggesting that the control systems for reproductive development in conifers and [[Truncated]]
    • (1995) Plant Mol Biol , vol.27 , pp. 69-78
    • Tandre1    Albert2    Sundas3    Engström4
  • 52
    • 0028306121 scopus 로고
    • Flower development and evolution: new answers and new questions
    • of special interest, A useful review suggesting that MADS-box genes are as interesting to evolutionary biologists as they are already to developmental biologists.
    • (1994) Proc Natl Acad Sci USA , vol.91 , pp. 5735-5737
    • Meyerowitz1
  • 53
    • 0025981848 scopus 로고
    • AGL1–AGL6, an Arabidopsis gene family with similarity to floral homeotic and transcription factor genes
    • (1991) Genes Dev , vol.5 , pp. 484-495
    • Ma1    Yanofsky2    Meyerowitz3
  • 54
    • 0028518740 scopus 로고
    • Spatially and temporally regulated expression of the MADS-box gene AGL2 in wild-type and mutant Arabidopsis flowers
    • of special interest, Describes the expression of AGL2, the prototype of a poorly defined subfamily of MADS-box genes. AGL2-like genes can be distinguished from the typical SQUAMOSA-like floral meristem-identity and A, B, and C-type flower organ-identity genes of the APETALA1, DEFICIENS/GLOBOSA and AGAMOUS-type by their sequence and expression pattern (Table 1). AGL2 is abundantly expressed throughout the floral meristem and in the primordia of all four types of floral organs. AGL2 expression is also high in developing ovules, embryos and seed coats. Except for plants transgenic for TM5 and FBP2 [27,38], no mutants of AGL2-like genes exist, so a detailed expression analysis is useful to get ideas about their function.
    • (1994) Plant Mol Biol , vol.26 , pp. 581-595
    • Flanagan1    Ma2
  • 55
    • 0028940289 scopus 로고
    • Molecular evolution of flower development: diversification of the plant MADS-box regulatory gene family
    • of special interest, Molecular analyses of plant MADS-box genes revealed appreciable differences in the substitution rates between different domains of these genes, with the MADS-box being the most highly conserved region. Furthermore, the phylogenetic analyses of Purugganan are in agreement with the subfamily structure described in this review (Table 1). The authors have also noted that the shared evolutionary history of members of a gene subfamily reflects the distinct functional roles these MADS-box genes play in flower development.
    • (1995) Genetics , vol.140 , pp. 345-356
    • Purugganan1    Rounsley2    Schmidt3    Yanofsky4
  • 56
    • 0028083395 scopus 로고
    • Evolution of a plant homeotic multigene family: toward connecting molecular systematics and molecular developmental genetics
    • (1994) Syst Biol , vol.43 , pp. 307-328
    • Doyle1
  • 59
    • 0028927730 scopus 로고
    • The CONSTANS gene of Arabidopsis promotes flowering and encodes a protein showing similarities to zinc finger transcription factors
    • of special interest, The authors describe the cloning of one of the first late flowering genes. They suggest that CONSTANS might function by activating floral meristem-identity genes.
    • (1995) Cell , vol.80 , pp. 847-857
    • Putterill1    Robson2    Lee3    Simon4    Coupland5
  • 60
    • 0028500824 scopus 로고
    • Control of Arabidopsis flower and seed development by the homeotic gene APETALA2
    • of special interest, Reports the cloning and analysis of APETALA2, which promotes the establishment of the floral meristem as well as regulating floral organ development by suppressing AGAMOUS gene expression in the 1° and 2° whorls. In addition, APETALA2 is required for normal seed coat development and, moreover, is even expressed in vegetative organs. Despite its function in determination of floral meristem and organ identity, APETALA2 is not a MADS-box gene, but encodes a member of a new class of plant regulatory proteins.
    • (1994) Plant Cell , vol.6 , pp. 1211-1225
    • Jofuku1    Den Boer2    Van Montagu3    Okamuro4
  • 62
    • 0028363397 scopus 로고
    • Arabidopsis floral homeotic gene BELL (BEL1) controls ovule development through negative regulation of AGAMOUS gene (AG)
    • of special interest, Presents a characterization of BEL1, a purely cadastral gene that directs normal integument development of ovules by suppressing AGAMOUS expression in this structure. The paper exemplarily demonstrates that the ‘ABC’ model needs some supplementation and extension to remain compatible with the increasing knowledge about the complexity of flower development.
    • (1994) Proc Natl Acad Sci USA , vol.91 , pp. 5761-5765
    • Ray1    Robinson-Beers2    Ray3    Baker4    Lang5    Preuss6    Milligan7    Gasser8
  • 63
    • 0028934476 scopus 로고
    • LEUNIG regulates AGAMOUS expression in Arabidopsis flowers
    • of special interest, Reports the identification and characterization of a novel cadastral gene, LEUNIG, with a role in Arabidopsis flower development. The data presented suggest that a key role of LEUNIG is to negatively regulate AGAMOUS expression in the first two whorls of the Arabidopsis flower and thus functions as a class A cadastral gene in A and C boundary establishment according to the ABC model (see text).
    • (1995) Development , vol.121 , pp. 975-991
    • Liu1    Meyerowitz2
  • 65
    • 0028244804 scopus 로고
    • Fimbriata controls flower development by mediating between meristem and organ identity genes
    • of outstanding interest, Reports the cloning of the FIMBRIATA gene from Antirrhinum majus. The authors show that the gene occupies an intermediate position in a sequence of gene activation that starts with the floral meristem-identity genes and leads to expression of the organ-identity genes in specific whorls of the floral meristem. It is interesting to note that FIMBRIATA is not a MADS-box gene. Rather, it encodes a product with no detectable homology to other known proteins.
    • (1994) Cell , vol.78 , pp. 99-107
    • Simon1    Carpenter2    Doyle3    Coen4
  • 66
    • 0028340607 scopus 로고
    • Flower colour intensity depends on specialized cell shape controlled by a Myb-related transcription factor
    • of special interest, Cloning of the MIXTA gene from Antirrhinum reveals that it encodes a Myb-related protein that probably participates in the transcriptional control of cell shape in petals. MIXTA is a strong candidate for being a target of the homeotic B function factors DEFICIENS and GLOBOSA.
    • (1994) Nature , vol.369 , pp. 661-664
    • Noda1    Glover2    Linstead3    Martin4
  • 68
    • 0025861808 scopus 로고
    • Molecular characterization of two stamen specific genes, tap1 and fil1, that are expressed in the wild type, but not in the deficiens mutant of Antirrhinum majus
    • (1991) Mol Gen Genet , vol.229 , pp. 129-136
    • Nacken1    Huijser2    Beltran3    Saedler4    Sommer5
  • 70
    • 0028364530 scopus 로고
    • Function and regulation of the Arabidopsis floral homeotic gene PISTILLATA
    • of special interest, Cloning and analysis of PISTALLATA makes it seem likely that it is the ortholog of the Antirrhinum gene GLOBOSA, much as APETALA3 is the ortholog of the Antirrhinum gene DEFICIENS. Thus, though Antirrhinum and Arabidopsis belong to different subclasses of dicots and are thought to have been diverging since the Cretaceous period, they both possess very similar pairs of interacting B function floral homeotic genes, DEFICIENS/GLOBOSA and APETALA3/PISTILLATA, respectively, beautifully illustrating the ‘synteny of functions’ between distantly related dicots.
    • (1994) Genes Dev , vol.8 , pp. 1548-1560
    • Goto1    Meyerowitz2
  • 75
    • 0028997265 scopus 로고
    • Homeotic genes and the regulation and evolution of insect wing number
    • of outstanding interest, The authors have investigated the role of homeotic genes in pterygote evolution by examining their function in Drosophila wing development and their expression in a primitive apterygote. They suggest that wings first arose without homeotic gene involvement in an ancestor with a homeotic ‘groundplan’ similar to modern winged insects, and that wing formation then fell under the negative control of individual homeotic genes at different stages of pterygote phylogeny.
    • (1995) Nature , vol.375 , pp. 58-61
    • Carroll1    Weatherbee2    Langeland3
  • 76
    • 0028171848 scopus 로고
    • Evolution of homeotic gene regulation and function in flies and butterflies
    • of outstanding interest, The authors have examined homeotic gene expression and regulation in butterflies and flies. They show that the difference in larval limb number between these species results from striking changes in bithorax-complex gene regulation in the butterfly abdomen. Moreover, high expression of the Ultrabithorax gene in hindwing imaginal discs of butterflies shows that the wing-patterning genes regulated by Ultrabithorax have diverged in the course of butterfly and fly evolution. These results suggest that changes in the number, size and pattern of homologous structures are most likely to involve changes in the timing and spatial regulation of existing genes, which in some cases are homeotic genes and in others are their downstream targets.
    • (1994) Nature , vol.372 , pp. 458-461
    • Warren1    Nagy2    Selegue3    Gates4    Carroll5
  • 77
    • 0026673151 scopus 로고
    • bicalyx is a natural homeotic floral variant
    • (1992) Nature , vol.358 , pp. 671-673
    • Ford1    Gottlieb2
  • 78
    • 0028973842 scopus 로고
    • The origin and early diversification of angiosperms
    • of special interest, An up-to-date review of angiosperm evolution from a palaeobotanist's point of view, maintaining that the major diversification of flowering plants occurred between ∼130 and 90 million years ago.
    • (1995) Nature , vol.374 , pp. 27-33
    • Crane1    Friis2    Pedersen3
  • 83
    • 12044255284 scopus 로고
    • Linking phylogeny and genetics: Zea mays as a tool for phylogenetic studies
    • (1993) Syst Biol , vol.42 , pp. 415-439
    • Kellogg1    Birchler2
  • 85
    • 0023239424 scopus 로고
    • Homeo boxes in the study of development
    • (1987) Science , vol.236 , pp. 1245-1252
    • Gehring1
  • 86
    • 0024206625 scopus 로고
    • Isolation and properties of cDNA clones encoding SRF, a transcription factor that binds to the c-fos serum response element
    • (1988) Cell , vol.55 , pp. 989-1003
    • Norman1    Runswick2    Pollock3    Treisman4
  • 87
    • 0026059946 scopus 로고
    • Expression of genes encoding the transcription factor SRF during early development of Xenopus laevis. identification of a CArG box-binding activity as SRF
    • (1991) EMBO J , vol.10 , pp. 933-940
    • Mohun1    Chambers2    Towers3    Taylor4
  • 88
    • 0023243470 scopus 로고
    • Characterization of two genes, ARGRI and ARGRIII required for specific regulation of arginine metabolism in yeast
    • (1987) Mol Gen Genet , vol.207 , pp. 142-148
    • Dubois1    Bercy2    Messenguy3
  • 89
  • 91
    • 0027048688 scopus 로고
    • Muscle-specific expression of SRF-related genes in the early embryo of Xenopus laevis
    • (1992) EMBO J , vol.11 , pp. 4981-4991
    • Chambers1    Kotecha2    Towers3    Mohun4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.