Skip to main content
Log in

Stamen specification and anther development in rice

  • Special Topic/Review/Developmental Genetics
  • Published:
Chinese Science Bulletin

Abstract

Male reproductive development is a complex biological process which includes the formation of the stamen with differentiated anther tissues, in which microspores/pollens are generated, then anther dehiscence and subsequently pollination. Stamen specification and anther development involve a number of extraordinary events such as meristem transition, cell division and differentiation, cell to cell communication, etc., which need the cooperative interaction of sporophytic and gametophytic genes. The advent of various tools for rice functional gene identification, such as complete genome sequence, genome-wide microarrays, collections of mutants, has greatly facilitated our understanding of mechanisms of rice stamen specification and anther development. Male sterile lines are critical for hybrid rice breeding, therefore understanding these processes will not only contribute greatly to the basic knowledge of crop developmental biology, but also to the development of new varieties for hybrid rice breeding in the future.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Similar content being viewed by others

References

  1. Scott R J, Spielman M, Dickinson H G. Stamen structure and function. Plant Cell, 2004, 16(Suppl): S46–S60

    Article  Google Scholar 

  2. Ma H. Molecular genetic analyses of microsporogenesis and microgametogenesis in flowering plants. Annu Rev Plant Biol, 2005, 56: 393–434

    Article  Google Scholar 

  3. Singh M B, Bhalla P L. Control of male germ-cell development in flowering plants. Bioessays, 2007, 29: 1124–1132

    Article  Google Scholar 

  4. Wilson Z A, Zhang D B. From Arabidopsis to rice: Pathways in pollen development. J Exp Bot, 2009, 60: 1479–1492; doi:10.1093/jxb/erp095

    Article  Google Scholar 

  5. Mercier R, Grelon M. Meiosis in plants: Ten years of gene discovery. Cytogenet Genome Res, 2008, 120: 281–290

    Article  Google Scholar 

  6. Coen E S, Meyerowitz E M. The war of the whorls: genetic interactions controlling flower development. Nature, 1991, 353: 31–37

    Article  Google Scholar 

  7. Ma H. The unfolding drama of flower development: Recent results from genetic and molecular analyses. Genes Dev, 1994, 8: 745–756

    Article  Google Scholar 

  8. Goldberg R B, Sanders P M, Beals T P. A novel cell-ablation strategy for studying plant development. Philos Trans R Soc London B Biol Sci, 1995, 350: 5–17

    Article  Google Scholar 

  9. Ma H, dePamphilis C. The ABCs of floral evolution. Cell, 2000, 101: 5–8

    Article  Google Scholar 

  10. Shimamoto K, Kyozuka J. Rice as a model for comparative genomics of plants. Annu Rev Plant Biol, 2002, 53: 399–419

    Article  Google Scholar 

  11. Weigel D, Jrgens G. Stem cells that make stems. Nature, 2002, 415: 751–754

    Google Scholar 

  12. Bortiri E, Hake S. Flowering and determinacy in maize. J Exp Bot, 2007, 58: 909–916

    Article  Google Scholar 

  13. Jung K H, An G, Ronald P C. Towards a better bowl of rice: assigning function to tens of thousands of rice genes. Nat Rev Genet, 2008, 9: 91–101

    Article  Google Scholar 

  14. IRGSP. The map-based sequence of the rice genome. Nature, 2005, 436: 793–800

    Article  Google Scholar 

  15. Clark L, Zhang W, Wendel J. A phylogeny of the Grass family (Poaceae) based on ndhF sequence data. Syst Bot, 1995, 20: 436–360

    Article  Google Scholar 

  16. Linder H, Rudall P. Evolutionary history of poales. Annu Rev Ecol Evol Syst, 2005, 36: 107–124

    Article  Google Scholar 

  17. Grass Phylogeny Working Group. Phylogeny and subfamilial classification of the grasses (Poaceae). Ann Mo Bot Gard, 2001, 88: 373–457

    Article  Google Scholar 

  18. Kellogg E A. Evolutionary history of the grasses. Plant Physiol, 2001, 125: 1198–1205

    Article  Google Scholar 

  19. Rudall P J, Stuppy W, Jennifer C, et al. Evolution of reproductive structures in grasses (Poaceae) inferred by sister-group comparison with their putative closest living relatives, Ecdeiocoleaceae. Am J Bot, 2005, 92: 1432–1443

    Article  Google Scholar 

  20. Zanis M J. Grass spilelet genetics and duplicate gene comparisons. Int J Plant Sci, 2007, 168: 93–110

    Article  Google Scholar 

  21. Rudall P J, Bateman R M. Evolution of zygomorphy in monocot flowers: iterative patterns and developmental constraints. New Phytologist, 2004, 162: 25–44

    Article  Google Scholar 

  22. Matsui T, Omasa K, Horie T. Mechanism of anther dehiscence in rice (Oryza sativa L.). Ann Bot, 1999, 84: 501–506

    Article  Google Scholar 

  23. Ikeda K, Nagasawa N, Nagato Y. Developmental course of inflorescence and spikelet in rice. Breeding Sci, 2004, 54: 147–156

    Article  Google Scholar 

  24. Itoh J, Nonomura K, Ikeda K, et al. Rice plant development: from zygote to spikelet. Plant Cell Physiol, 2005, 46: 23–47

    Article  Google Scholar 

  25. Feng J H, Lu Y G, Liu X D, et al. Pollen development and its stages in rice (Oryza sativa L.). Chinese J Rice Sci, 2001, 15: 21–28

    Google Scholar 

  26. Li N, Zhang D S, Liu H S, et al. The rice Tapetum Degeneration Retardation gene is required for tapetum degradation and anther development. Plant Cell, 2006, 18: 2999–3014

    Article  Google Scholar 

  27. Sanders P M, Bui A Q, Weterings K, et al. Anther developmental defects in Arabidopsis thaliana male-sterile mutants. Sex. Plant Reprod, 1999, 11: 297–322

    Article  Google Scholar 

  28. Clark S E, Schiefelbein J W. Expanding insights into the role of cell proliferation in plant development. Trends Cell Biol, 1997, 7: 454–458

    Article  Google Scholar 

  29. Jeong S, Trotochaud A, Clark S. The Arabidopsis CLAVATA2 gene encodes a receptor-like protein required for the stability of the CLAVATA1 receptor-like kinase. Plant Cell, 1999, 11: 1925–1933

    Article  Google Scholar 

  30. Fletcher J C, Brand U, Running M P, et al. Signaling of cell fate decisions by CLAVATA3 in Arabidopsis shoot meristems. Science, 1999, 283: 1911–1914

    Article  Google Scholar 

  31. Clark S E, Running M P, Meyerowitz E M. CLAVATA1, a regulator of meristem and flower development in Arabidopsis. Development, 1993, 119: 397–418

    Google Scholar 

  32. Clark S, Running M, Meyerowitz E. CLAVATA3 is a specific regulator of shoot and floral meristem development affecting the same processes as CLAVATA1. Development, 1995, 121: 2057–2067

    Google Scholar 

  33. Kayes J M, Clark S E. CLAVATA2, a regulator of meristem and organ development in Arabidopsis. Development, 1998, 125: 3843–3851

    Google Scholar 

  34. Muller R, Bleckmann A, Simon R. The receptor kinase CORYNE of Arabidopsis transmits the stem cell-limiting signal CLAVATA3 independently of CLAVATA1. Plant Cell, 2008, 20: 934–946

    Article  Google Scholar 

  35. Barton M, Poethig R. Formation of the shoot apical meristem in Arabidopsis thaliana: An analysis of development in the wild type and shoot meristemless mutant. Development, 1993, 119: 823–831

    Google Scholar 

  36. Clark S E, Jacobsen S E, Levin J Z, et al. The CLAVATA and SHOOT MERISTEMLESS loci competitively regulate meristem activity in Arabidopsis. Development, 1996, 122: 1567–1575

    Google Scholar 

  37. Endrizzi K, Moussian B, Haecker A, et al. The SHOOT MERISTEMLESS gene is required for maintenance of undifferentiated cells in Arabidopsis shoot and floral meristems and acts at a different regulatory level than the meristem genes WUSCHEL and ZWILLE. Plant J, 1996, 10: 967–979

    Article  Google Scholar 

  38. Laux T, Mayer K F, Berger J, et al. The WUSCHEL gene is required for shoot and floral meristem integrity in Arabidopsis. Development, 1996, 122: 87–96

    Google Scholar 

  39. Brand U, Fletcher J, Hobe M, et al. Dependence of stem cell fate in Arabidopsis on a feedback loop regulated by CLV3 activity. Science, 2000, 289: 617–619

    Article  Google Scholar 

  40. Schoof H, Lenhard M, Haecker A, et al. The stem cell population of Arabidopsis shoot meristems is maintained by a regulatory loop between the CLAVATA and WUSCHEL genes. Cell, 2000, 100: 635–644

    Article  Google Scholar 

  41. Muller R, Borghi L, Kwiatkowska D, et al. Dynamic and compensatory responses of Arabidopsis shoot and floral meristems to CLV3 signaling. Plant Cell, 2006, 18: 1188–1198

    Article  Google Scholar 

  42. Taguchi-Shiobara F, Yuan Z, Hake S, et al. The fasciated ear2 gene encodes a leucine-rich repeat receptor-like protein that regulates shoot meristem proliferation in maize. Genes Dev, 2001, 15: 2755–2766

    Article  Google Scholar 

  43. Bommert P, Lunde C, Nardmann J, et al. thick tassel dwarf1 encodes a putative maize ortholog of the Arabidopsis CLAVATA1 leucinerich repeat receptor-like kinase. Development, 2005, 132: 1235–1245

    Article  Google Scholar 

  44. Suzaki T, Sato M, Ashikari M, et al. The gene FLORAL ORGAN NUMBER1 regulates floral meristem size in rice and encodes a leucine-rich repeat receptor kinase orthologous to Arabidopsis CLAVATA1. Development, 2004, 131: 5649–5657

    Article  Google Scholar 

  45. Kim C, Jeong D, An G. Molecular cloning and characterization of OsLRK1 encoding a putative receptor-like protein kinase from Oryza sativa. Plant Sci, 2000, 152: 17–26

    Article  Google Scholar 

  46. Chu H, Qian Q, Liang W Q, et al. The Floral Organ Number4 gene encoding a putative ortholog of Arabidopsis CLAVATA3 regulates apical meristem size in rice. Plant Physiol, 2006, 142: 1039–1052

    Article  Google Scholar 

  47. Suzaki T, Toriba T, Fujimoto M, et al. Conservation and diversification of meristem maintenance mechanism in Oryza sativa: Function of the FLORAL ORGAN NUMBER2 gene. Plant Cell Physiol, 2006, 47: 1591–1602

    Article  Google Scholar 

  48. Chu H, Zhang D. The shoot apical meristem size regulated by FON4 in rice. Plant Signal Behav, 2007, 2: e1–e2

    Google Scholar 

  49. Fornara F, Marziani G, Mizzi L, et al. MADS-box genes controlling flower development in rice. Plant Biol, 2003, 1: 16–22

    Article  Google Scholar 

  50. Theissen G, Becker A. The ABCs of flower development in Arabidopsis and rice. Prog Bot, 2004, 65: 193–215

    Google Scholar 

  51. Kater M M, Dreni L, Colombo L. Functional conservation of MADS-box factors controlling floral organ identity in rice and Arabidopsis. J Exp Bot, 2006, 57: 3433–3444

    Article  Google Scholar 

  52. Hirano H Y, Hirai A, Sano Y, et al., eds. Rice biology in the genomics era. Ser: Biotechnology in Agriculture and Forestry. Berlin Heidelberg: Springer, 2008

  53. Pelaz S, Ditta G S, Baumann E, et al. B and C floral organ identity functions require SEPALLATA MADS-box genes. Nature, 2000, 405: 200–203

    Article  Google Scholar 

  54. Ditta G, Pinyopich A, Robles P, et al. The SEP4 gene of Arabidopsis thaliana functions in floral organ and meristem identity. Curr Biol, 2004, 14: 1935–1940

    Article  Google Scholar 

  55. Lohmann J U, Weigel D. Building beauty: the genetic control of floral patterning. Dev Cell, 2002, 2: 135–142

    Article  Google Scholar 

  56. Jack T. Molecular and genetic mechanisms of floral control. Plant Cell, 2004, 16: S1–S17

    Article  Google Scholar 

  57. Moon Y H, Jung J Y, Kang H G, et al. Identification of a rice APETALA3 homologue by yeast two-hybrid screening. Plant Mol Biol, 1999, 40: 167–177

    Article  Google Scholar 

  58. Nagasawa N, Miyoshi M, Sano Y, et al. SUPERWOMAN1 and DROOPING LEAF genes control floral organ identity in rice. Development, 2003, 130: 705–718

    Article  Google Scholar 

  59. Chung Y Y, Kim S R, Kang H G, et al. Characterization of two rice MADS box genes homologous to GLOBOSA. Plant Sci, 1995, 109: 45–56

    Article  Google Scholar 

  60. Lee S, Jeon J S, An K, et al. Alteration of floral organ identity in rice through ectopic expression of OsMADS16. Planta, 2003, 217: 904–911

    Article  Google Scholar 

  61. Yamaguchi T, Lee DY, Miyao A, et al. Functional diversification of the two C-class MADS box genes OSMADS3 and OSMADS58 in Oryza sativa. Plant Cell, 2006, 18: 15–28

    Article  Google Scholar 

  62. Kang H G, Jeon J S, Lee S, et al. Identification of class B and class C floral organ identity genes from rice plants. Plant Mol Biol, 1998, 38: 1021–1029

    Article  Google Scholar 

  63. Prasad K, Vijayraghavan U. Double-stranded RNA interference of a rice PI/GLO paralog, OsMADS2, uncovers its second-whorl-specific function in floral organ patterning. Genetics, 2003, 165: 2301–2305

    Google Scholar 

  64. Yadav S R, Prasad K, Vijayraghavan U. Divergent regulatory OsMADS2 functions control size, shape and differentiation of the highly derived rice floret second-whorl organ. Genetics, 2007, 176: 283–294

    Article  Google Scholar 

  65. Yoshida H, Itoh J, Ohmori S, et al. Superwoman1-cleistogamy, a hopeful allele for gene containment in GM rice. Plant Biotechnol J, 2007, 5: 835–846

    Article  Google Scholar 

  66. Yao S G, Ohmori S, Kimizu M, et al. Unequal genetic redundancy of rice PISTILLATA orthologs, OsMADS2 and OsMADS4, in lodicule and stamen development. Plant Cell Physiol, 2008, 49: 853–857

    Article  Google Scholar 

  67. Yanofsky M F, Ma H, Bowman J L, et al. The protein encoded by the Arabidopsis homeotic gene Agamous resembles transcription factors. Nature, 1990, 346: 35–39

    Article  Google Scholar 

  68. Kang H G, Noh Y S, Chung Y Y, et al. Phenotypic alterations of petal and sepal by ectopic expression of a rice MADS box gene in tobacco. Plant Mol Biol, 1995, 29: 1–10

    Article  Google Scholar 

  69. Lopez-Dee Z P, Wittich P, Enrico Pe M, et al. OsMADS13, a novel rice MADS-box gene expressed during ovule development. Dev Genet, 1999, 25: 237–244

    Article  Google Scholar 

  70. Lee S, Kim J, Son J S, et al. Systematic reverse genetic screening of T-DNA tagged genes in rice for functional genomic analyses: MADS-box genes as a test case. Plant Cell Physiol, 2003, 44: 1403–1411

    Article  Google Scholar 

  71. Kang S G, Hannapel D J. Nucleotide sequences of novel potato (Solanum tuberosum L.) MADS-box cDNAs and their expression in vegetative organs. Gene, 1995, 166: 329–330

    Article  Google Scholar 

  72. Kyozuka J, Kobayashi T, Morita M, et al. Spatially and temporally regulated expression of rice MADS box genes with similarity to Arabidopsis class A, B and C genes. Plant Cell Physiol, 2000, 41: 710–718

    Google Scholar 

  73. Kyozuka J, Shimamoto K. Ectopic expression of OsMADS3, a rice ortholog of AGAMOUS, caused a homeotic transformation of lodicules to stamens in transgenic rice plants. Plant Cell Physiol, 2002, 43: 130–135

    Article  Google Scholar 

  74. Dreni L, Jacchia S, Fornara F, et al. The D-lineage MADS-box gene OsMADS13 controls ovule identity in rice. Plant J, 2007, 52: 690–699

    Article  Google Scholar 

  75. Nagasawa N, Miyoshi M, Sano Y, et al. SUPERWOMAN1 and DROOPING LEAF genes control floral organ identity in rice. Development, 2003, 130: 705–718

    Article  Google Scholar 

  76. Yamaguchi T, Nagasawa N, Kawasaki S, et al. The YABBY gene DROOPING LEAF regulates carpel specification and midrib development in Oryza sativa. Plant Cell, 2004, 16: 500–509

    Article  Google Scholar 

  77. Chung Y Y, Kim S R, Finkel D, et al. Early flowering and reduced apical dominance result from ectopic expression of a rice MADS box gene. Plant Mol Biol, 1994, 26: 657–665

    Article  Google Scholar 

  78. Greco R, Stagi L, Colombo L, et al. MADS box genes expressed in developing inflorescences of rice and sorghum. Mol Gen Genet, 1997, 253: 615–623

    Article  Google Scholar 

  79. Kang H G, An G. Isolation and characterization of a rice MADS box gene belonging to the AGL2 gene family. Mol Cells, 1997, 7: 45–51

    Google Scholar 

  80. Kang H G, Jang S, Chung J E, et al. Characterization of two rice MADS box genes that control flowering time. Mol Cells, 1997, 7: 559–566

    Google Scholar 

  81. Malcomber S T, Kellogg E A. Heterogeneous expression patterns and separate roles of the SEPALLATA gene LEAFY HULL STERILE1 in grasses. Plant Cell, 2004, 16, 1692–1706

    Article  Google Scholar 

  82. Pelucchi N, Fornara F, Favalli C, et al. Comparative analysis of MADS-box genes expressed during flower development. Sexual Plant Reproduction, 2002, 15: 113–122

    Article  Google Scholar 

  83. Jeon J S, Jang S, Lee S, et al. leafy hull sterile1 is a homeotic mutation in a rice MADS box gene affecting rice flower development. Plant Cell, 2000, 12: 871–884

    Article  Google Scholar 

  84. Lim J, Moon Y H, An G, et al. Two rice MADS domain proteins interact with OsMADS1. Plant Mol Biol, 2000, 44: 513–527

    Article  Google Scholar 

  85. Prasad K, Sriram P, Kumar C S, et al. Ectopic expression of rice OsMADS1 reveals a role in specifying the lemma and palea, grass floral organs analogous to sepals. Dev Genes Evol, 2001, 211: 281–290

    Article  Google Scholar 

  86. Agrawal G K, Abe K, Yamazaki M, et al. Conservation of the E-function for floral organ identity in rice revealed by the analysis of tissue culture-induced loss-of-function mutants of the OsMADS1 gene. Plant Mol Biol, 2005, 59: 125–135

    Article  Google Scholar 

  87. Prasad K, Parameswaran S, Vijayraghavan U. OsMADS1, a rice MADS-box factor, controls differentiation of specific cell types in the lemma and palea and is an early-acting regulator of inner floral organs. Plant J, 2005, 43: 915–928

    Article  Google Scholar 

  88. Chen Z X, Wu J G, Ding W N, et al. Morphogenesis and molecular basis on naked seed rice, a novel homeotic mutation of OsMADS1 regulating transcript level of AP3 homologue in rice. Planta, 2006, 223: 882–890

    Article  Google Scholar 

  89. Khush G S, Librojo A J. Naked seed rice (NSR) is allelic to op and lhs. Rice Genet News, 1985, 2: 71

    Google Scholar 

  90. Ikeda K, Nagasawa N, Nagato Y. ABERRANT PANICLE ORGANIZATION 1 temporally regulates meristem identity in rice. Dev Biol, 2005, 282: 349–360

    Article  Google Scholar 

  91. Ikeda K, Ito M, Nagasawa N, et al. Rice ABERRANT PANICLE ORGANIZATION 1, encoding an F-box protein, regulates meristem fate. Plant J, 2007, 51: 1030–1040

    Article  Google Scholar 

  92. Luo H, Li Y, Yang Z, et al. Fine mapping of a pistilloid-stamen (PS) gene on the short arm of chromosome 1 in rice. Genome, 2006, 49: 1016–1022

    Article  Google Scholar 

  93. Endo M, Tsuchiya T, Saito H, et al. Identification and molecular characterization of novel anther-specific genes in Oryza sativa L. by using cDNA microarray. Genes Genet Syst, 2004, 79: 213–226

    Article  Google Scholar 

  94. Lan L, Chen W, Lai Y, et al. Monitoring of gene expression profiles and isolation of candidate genes involved in pollination and fertilization in rice (Oryza sativa L.) with a 10K cDNA microarray. Plant Mol Biol, 2004, 54: 471–487

    Article  Google Scholar 

  95. Yamaguchi T, Nakayama K, Hayashi T, et al. cDNA microarray analysis of rice anther genes under chilling stress at the microsporogenesis stage revealed two genes with DNA transposon Castaway in the 5’-flanking region. Biosci Biotechnol Biochem, 2004, 68: 1315–1323

    Article  Google Scholar 

  96. Jung K H, Han M J, Lee Y S, et al. Rice Undeveloped Tapetum1 is a major regulator of early tapetum development. Plant Cell, 2005, 17: 2705–2722

    Article  Google Scholar 

  97. Wang Z, Liang Y, Li C, et al. Microarray analysis of gene expression involved in anther development in rice (Oryza sativa L.). Plant Mol Biol, 2005, 58: 721–737

    Article  Google Scholar 

  98. Li M, Xu W, Yang W, et al. Genome-wide gene expression profiling reveals conserved and novel molecular functions of the stigma in rice. Plant Physiol, 2007, 144: 1797–1812

    Article  Google Scholar 

  99. Hirano K, Aya K, Hobo T, et al. Comprehensive transcriptome analysis of phytohormone biosynthesis and signaling genes in microspore/pollen and tapetum of rice. Plant Cell Physiol, 2008, 49: 1429–1450

    Article  Google Scholar 

  100. Hobo T, Suwabe K, Aya K, et al. Various spatiotemporal expression profiles of anther-expressed genes in rice. Plant Cell Physiol, 2008, 49: 1417–1428

    Article  Google Scholar 

  101. Suwabe K, Suzuki G, Takahashi H, et al. Separated transcriptomes of male gametophyte and tapetum in rice: Validity of a laser microdissection (LM) microarray. Plant Cell Physiol, 2008, 49: 1407–1416

    Article  Google Scholar 

  102. Huang S X, Wu H Q, Li Y R, et al. Competitive interaction between two functional S-haplotypes confer self-compatibility on tetraploid Chinese cherry (Prunus pseudocerasus Lindl. CV. Nanjing Chuisi). Plant Cell Rep, 2008, 27: 1075–1085

    Article  Google Scholar 

  103. Tan H X, Wen T Q, Zhang D B. Molecular mechanisms of pollen development in Oryza sativa (in Chinese). Chinese Bull Bot, 2007, 24: 330–339

    Google Scholar 

  104. Wang Y, Wang Y F, Zhang D B. Identification of the rice (Oryza sativa L.) mutant msp1-4 and expression analysis of its UDT1 and GAMYB genes. J Plant Physiol Mol Biol, 2006, 32: 527–534

    Google Scholar 

  105. Nonomura K, Miyoshi K, Eiguchi M, et al. The MSP1 gene is necessary to restrict the number of cells entering into male and female sporogenesis and to initiate anther wall formation in rice. Plant Cell, 2003, 15: 1728–1739

    Article  Google Scholar 

  106. Zhao X, de Palma J, Oane R, et al. OsTDL1A binds to the LRR domain of rice receptor kinase MSP1, and is required to limit sporocyte numbers. Plant J, 2008, 54: 375–387

    Article  Google Scholar 

  107. Nonomura K I, Nakano M, Murata K, et al. An insertional mutation in the rice PAIR2 gene, the ortholog of Arabidopsis ASY1, results in a defect in homologous chromosome pairing during meiosis. Mol Genet Genomics, 2004, 271: 121–129

    Article  Google Scholar 

  108. Nonomura K, Nakano M, Eiguchi M, et al. PAIR2 is essential for homologous chromosome synapsis in rice meiosis I. J Cell Sci, 2006, 119: 217–225

    Article  Google Scholar 

  109. Nonomura K, Nakano M, Fukuda T, et al. The novel gene HOMOLOGOUS PAIRING ABERRATION IN RICE MEIOSIS1 of rice encodes a putative coiled-coil protein required for homologous chromosome pairing in meiosis. Plant Cell, 2004, 16: 1008–1020

    Article  Google Scholar 

  110. Zhang L, Tao J, Wang S, et al. The rice OsRad21-4, an orthologue of yeast Rec8 protein, is required for efficient meiosis. Plant Mol Biol, 2006, 60: 533–554

    Article  Google Scholar 

  111. Nonomura K, Morohoshi A, Nakano M, et al. A germ cell specific gene of the ARGONAUTE family is essential for the progression of premeiotic mitosis and meiosis during sporogenesis in rice. Plant Cell, 2007, 19: 2583–2594

    Article  Google Scholar 

  112. Zhang D S, Liang W Q, Yuan Z, et al. Tapetum Degeneration Retardation is critical for aliphatic metabolism and gene regulation during rice pollen development. Mol Plant, 2008, 1: 599–610

    Article  Google Scholar 

  113. Sorensen A M, Krober S, Unte U S, et al. The Arabidopsis ABORTED MICROSPORES (AMS) gene encodes a MYC class transcription factor. Plant J, 2003, 33: 413–423

    Article  Google Scholar 

  114. Wilson Z A, Morroll S M, Dawson J, et al. The Arabidopsis MALE STERILITY1 (MS1) gene is a transcriptional regulator of male gametogenesis, with homology to the PHD-finger family of transcription factors. Plant J, 2001, 28: 27–39

    Article  Google Scholar 

  115. Ito T, Shinozaki K. The MALE STERILITY1 gene of Arabidopsis, encoding a nuclear protein with a PHD-finger motif, is expressed in tapetal cells and is required for pollen maturation. Plant Cell Physiol, 2002, 43: 1285–1292

    Article  Google Scholar 

  116. Ito T, Nagata N, Yoshiba Y, et al. Arabidopsis MALE STERILITY1 encodes a PHD-Type transcription factor and regulates pollen and tapetum development. Plant Cell, 2007, 19: 3549–3562

    Article  Google Scholar 

  117. Yang C, Vizcay-Barrena G, Conner K, et al. MALE STERILITY1 is required for tapetal development and pollen wall biosynthesis. Plant Cell, 2007, 19: 3530–3548

    Article  Google Scholar 

  118. Kaneko M, Inukai Y, Ueguchi-Tanaka M, et al. Loss-of-function mutations of the rice GAMYB gene impair alpha-amylase expression in aleurone and flower development. Plant Cell, 2004, 16: 33–44

    Article  Google Scholar 

  119. Tsuji H, Aya K, Ueguchi-Tanaka M, et al. GAMYB controls different sets of genes and is differentially regulated by microRNA in aleurone cells and anthers. Plant J, 2006, 47: 427–444

    Article  Google Scholar 

  120. Wang A, Xia Q, Xie W, et al. The classical Ubisch bodies carry a sporophytically produced structural protein (RAFTIN) that is essential for pollen development. Proc Natl Acad Sci USA, 2003, 100: 14487–14492

    Article  Google Scholar 

  121. Winter H, Huber S C. Regulation of sucrose metabolism in higher plants: Localization and regulation of activity of key enzymes. Crit Rev Biochem Mol Biol, 2000, 35: 253–289

    Article  Google Scholar 

  122. Chen R, Zhao X, Shao Z, et al. Rice UDP-glucose pyrophosphorylase1 is essential for pollen callose deposition and its cosuppression results in a new type of thermosensitive genic male sterility. Plant Cell, 2007, 19: 847–861

    Article  Google Scholar 

  123. Mermall V, Post P L, Mooseker M S. Unconventional myosins in cell movement, membrane traffic, and signal transduction. Science, 1998, 279: 527–533

    Article  Google Scholar 

  124. Berg J S, Powell B C, Cheney R E. A millennial myosin census. Mol Biol Cell, 2001, 12: 780–794

    Google Scholar 

  125. Jiang S Y, Cai M, Ramachandran S. ORYZA SATIVA MYOSIN XI B controls pollen development by photoperiod-sensitive protein localizations. Dev Biol, 2007, 304: 579–592

    Article  Google Scholar 

  126. Han M J, Jung K H, Yi G, et al. Rice Immature Pollen 1 (RIP1) is a regulator of late pollen development. Plant Cell Physiol, 2006, 47: 1457–1472

    Article  Google Scholar 

  127. Jung K H, Han M J, Lee D Y, et al. Wax-deficient anther1 is involved in cuticle and wax production in rice anther walls and is required for pollen development. Plant Cell, 2006, 18: 3015–3032

    Article  Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to DaBing Zhang.

Additional information

Supported by the National Key Basic Research Development Program of China (Grant Nos. 2007CB108700, 2009CB941500), National Natural Science Foundation of China (Grant No. 30725022), and Shanghai Leading Academic Discipline Project (Grant No. B205)

About this article

Cite this article

Zhang, D., Wilson, Z.A. Stamen specification and anther development in rice. Chin. Sci. Bull. 54, 2342–2353 (2009). https://doi.org/10.1007/s11434-009-0348-3

Download citation

  • Received:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s11434-009-0348-3

Keywords

Navigation