FILAMENTOUS FLOWER, a meristem and organ identity gene of Arabidopsis, encodes a protein with a zinc finger and HMG-related domains.

Distinctive from that of the animal system, the basic plan of the plant body is the continuous formation of a structural unit, composed of a stem with a meristem at the top and lateral organs continuously forming at the meristem. Therefore, mechanisms controlling the formation, maintenance, and development of a meristem will be a key to understanding the body plan of higher plants. Genetic analyses of filamentous flower (fil) mutants have indicated that FIL is required for the maintenance and growth of inflorescence and floral meristems, and of floral organs of Arabidopsis thaliana. FIL encodes a protein carrying a zinc finger and a HMG box-like domain, which is known to work as a transcription regulator. As expected, the FIL protein was shown to have a nuclear location. In situ hybridization clearly demonstrated that FIL is expressed only at the abaxial side of primordia of leaves and floral organs. Transgenic plants, ectopically expressing FIL, formed filament-like leaves with randomly arranged cells at the leaf margin. Our results indicate that cells at the abaxial side of the lateral organs are responsible for the normal development of the organs as well as for maintaining the activity of meristems.

[1]  P. Masson,et al.  The PINHEAD/ZWILLE gene acts pleiotropically in Arabidopsis development and has overlapping functions with the ARGONAUTE1 gene. , 1999, Development.

[2]  K. Okada,et al.  FILAMENTOUS FLOWER Controls the Formation and Development of Arabidopsis Inflorescences and Floral Meristems , 1999, Plant Cell.

[3]  J. R. McConnell,et al.  Leaf polarity and meristem formation in Arabidopsis. , 1998, Development.

[4]  T. Nelson,et al.  Leafbladeless1 is required for dorsoventrality of lateral organs in maize. , 1998, Development.

[5]  K. Grasser HMG1 and HU proteins : architectural elements in plant chromatin , 1998 .

[6]  H. Takatsuji,et al.  Zinc-finger transcription factors in plants , 1998, Cellular and Molecular Life Sciences CMLS.

[7]  A. Hudson,et al.  The PHANTASTICA Gene Encodes a MYB Transcription Factor Involved in Growth and Dorsoventrality of Lateral Organs in Antirrhinum , 1998, Cell.

[8]  G. Jürgens,et al.  Role of the ZWILLE gene in the regulation of central shoot meristem cell fate during Arabidopsis embryogenesis , 1998, The EMBO journal.

[9]  D. Bouchez,et al.  AGO1 defines a novel locus of Arabidopsis controlling leaf development , 1998, The EMBO journal.

[10]  A. Lee Vascular Dementia , 2011, Chonnam medical journal.

[11]  S. Moose,et al.  A maize zinc-finger protein binds the prolamin box in zein gene promoters and interacts with the basic leucine zipper transcriptional activator Opaque2. , 1997, Proceedings of the National Academy of Sciences of the United States of America.

[12]  C. Dean,et al.  A Novel Zinc Finger Protein Is Encoded by the Arabidopsis LSD1 Gene and Functions as a Negative Regulator of Plant Cell Death , 1997, Cell.

[13]  R. Poethig,et al.  Phase change and the regulation of trichome distribution in Arabidopsis thaliana. , 1997, Development.

[14]  Takanori Hirano,et al.  Engineered GFP as a vital reporter in plants , 1996, Current Biology.

[15]  R. Reeves,et al.  High-mobility-group chromosomal proteins: architectural components that facilitate chromatin function. , 1996, Progress in nucleic acid research and molecular biology.

[16]  R. Foley,et al.  Interactions between distinct types of DNA binding proteins enhance binding to ocs element promoter sequences. , 1995, The Plant cell.

[17]  Detlef Weigel,et al.  A developmental switch sufficient for flower initiation in diverse plants , 1995, Nature.

[18]  A. Hudson,et al.  Phantastica: a gene required for dorsoventrality of leaves in Antirrhinum majus , 1995 .

[19]  A. Gronenborn,et al.  Molecular basis of human 46X,Y sex reversal revealed from the three-dimensional solution structure of the human SRY-DNA complex , 1995, Cell.

[20]  K. Grasser Plant chromosomal high mobility group (HMG) proteins. , 1995, The Plant journal : for cell and molecular biology.

[21]  M. Yanofsky,et al.  Molecular basis of the cauliflower phenotype in Arabidopsis , 1995, Science.

[22]  X. Deng,et al.  Light inactivation of arabidopsis photomorphogenic repressor COP1 involves a cell-specific regulation of its nucleocytoplasmic partitioning , 1994, Cell.

[23]  Elliot M. Meyerowitz,et al.  The ABCs of floral homeotic genes , 1994, Cell.

[24]  Elliot M. Meyerowitz,et al.  Control of flower development in Arabidopsis thaliana by APETALA1 and interacting genes , 1993 .

[25]  Cindy Gustafson-Brown,et al.  Molecular characterization of the Arabidopsis floral homeotic gene APETALA1 , 1992, Nature.

[26]  D. Weigel,et al.  LEAFY controls floral meristem identity in Arabidopsis , 1992, Cell.

[27]  J. Bowman,et al.  Negative regulation of the Arabidopsis homeotic gene AGAMOUS by the APETALA2 product , 1991, Cell.

[28]  D. A. Clayton,et al.  Similarity of human mitochondrial transcription factor 1 to high mobility group proteins. , 1991, Science.

[29]  K. Okada,et al.  Isolation and characterization of novel mutants of Arabidopsis thaliana defective in flower development , 1988 .

[30]  F. Nagy,et al.  Identification of DNA sequences required for activity of the cauliflower mosaic virus 35S promoter , 1985, Nature.

[31]  John E. Shelton People's Republic of China , 1973 .