Skip to main content
Log in

Genetic regulation of maize flower development and sex determination

  • Review
  • Published:
Planta Aims and scope Submit manuscript

Abstract

Main conclusion

The determining process of pistil fate are central to maize sex determination, mainly regulated by a genetic network in which the sex-determining genes SILKLESS 1 , TASSEL SEED 1 , TASSEL SEED 2 and the paramutagenic locus Required to maintain repression 6 play pivotal roles.

Maize silks, which emerge from the ear shoot and derived from the pistil, are the functional stigmas of female flowers and play a pivotal role in pollination. Previous studies on sex-related mutants have revealed that sex-determining genes and phytohormones play an important role in the regulation of flower organogenesis. The processes determining pistil fate are central to flower development, where a silk identified gene SILKLESS 1 (SK1) is required to protect pistil primordia from a cell death signal produced by two commonly known genes, TASSEL SEED 1 (TS1) and TASSEL SEED 2 (TS2). In this review, maize flower developmental process is presented together with a focus on important sex-determining mutants and hormonal signaling affecting pistil development. The role of sex-determining genes, microRNAs, phytohormones, and the paramutagenic locus Required to maintain repression 6 (Rmr6), in forming a regulatory network that determines pistil fate, is discussed. Cloning SK1 and clarifying its function were crucial in understanding the regulation network of sex determination. The signaling mechanisms of phytohormones in sex determination are also an important research focus.

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.

Fig. 1
Fig. 2
Fig. 3
Fig. 4

Similar content being viewed by others

References

  • Acosta IF, Laparra H, Romero SP, Schmelz E, Hamberg M, Mottinger JP, Moreno MA, Dellaporta SL (2009) tasselseed1 is a lipoxygenase affecting jasmonic acid signaling in sex determination of maize. Science 323:262–265

    Article  CAS  PubMed  Google Scholar 

  • Ambrose BA, Lerner DR, Ciceri P, Padilla CM, Yanofsky MF, Schmidt RJ (2000) Molecular and genetic analyses of the silky1 gene reveal conservation in floral organ specification between eudicots and monocots. Mol Cell 5:569–579

    Article  CAS  PubMed  Google Scholar 

  • Balibrea Lara ME, Gonzalez Garcia MC, Fatima T, Ehness R, Lee TK, Proels R, Tanner W, Roitsch T (2004) Extracellular invertase is an essential component of cytokinin-mediated delay of senescence. Plant Cell 16:1276–1287

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Banks JN (2008) MicroRNA, sex determination and floral meristem determinacy in maize. Genome Biol 91:204

    Article  CAS  Google Scholar 

  • Bartlett ME, Williams SK, Taylor Z, DeBlasio S, Goldshmidt A, Hall DH, Schmidt RJ, Jackson DP, Whipple CJ (2015) The maize PI/GLO ortholog Zmm16/sterile tassel silky ear1 interacts with the zygomorphy and sex determination pathways in flower development. Plant Cell 27:3081–3098

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Bensen RJ, Johal GS, Crane VC, Tossberg JT, Schnable PS, Meeley RB, Briggs SP (1995) Cloning and characterization of the maize an1 gene. Plant Cell 7:75–84

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Bolduc N, Yilmaz A, Mejia-Guerra MK, Morohashi K, O’Connor D, Grotewold E, Hake S (2012) Unraveling the KNOTTED1 regulatory network in maize meristems. Genes Dev 26:1685–1690

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Bommert P, Lunde C, Nardmann J, Vollbrecht E, Running M, Jackson D, Hake S, Werr W (2005a) thick tassel dwarf1 encodes a putative maize ortholog of the Arabidopsis CLAVATA1 leucine-rich repeat receptor-like kinase. Development 132:1235–1245

    Article  CAS  PubMed  Google Scholar 

  • Bommert P, Satoh-Nagasawa N, Jackson D, Hiran HY (2005b) Genetics and evolution of inflorescence and flower development in grasses. Plant Cell Physiol 46:69–78

    Article  CAS  PubMed  Google Scholar 

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

    Article  CAS  PubMed  Google Scholar 

  • Bortiri E, Chuck G, Vollbrecht E, Rocheford T, Martienssen R, Hake S (2006) ramosa2 encodes a LATERAL ORGAN BOUNDARY domain protein that determines the fate of stem cells in branch meristems of maize. Plant Cell 18:574–585

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Cacharrón J, Saedler H, Theißen G (1999) Expression of MADS-box genes ZMM8 and ZMM14 during inflorescence development of Zea mays discriminates between the upper and the lower floret of each spikelet. Dev Genes Evol 209:411–420

    Article  Google Scholar 

  • Calderon-Urrea A, Dellaporta SL (1999) Cell death and cell protection genes determine the fate of pistils in maize. Development 126:435–441

    CAS  PubMed  Google Scholar 

  • Cheng PC, Greyson RI, Walden DB (1983) Organ initiation and the development of unisexual flowers in the tassel and ear of Zea mays. Am J Bot 70:450–462

    Article  Google Scholar 

  • Cheng H, Song S, Xiao L, Soo HM, Cheng Z, Xie D, Peng J (2009) Gibberellin acts through jasmonate to control the expression of MYB21, MYB24, and MYB57 to promote stamen filament growth in Arabidopsis. PLoS Genet 5:e1000440

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Chuck G (2010) Molecular mechanisms of sex determination in monoecious and dioecious plants. Adv Bot Res 54:53–83

    Article  CAS  Google Scholar 

  • Chuck G, Meeley R, Hake S (1998) The control of maize spikelet meristem fate by the APETALA2-like gene indeterminate spikelet1. Genes Dev 12:1145–1154

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Chuck G, Muszynski M, Kellogg E, Hake S, Schmidt RJ (2002) The control of spikelet meristem identity by the branched silkless1 gene in maize. Science 298:1238–1241

    Article  CAS  PubMed  Google Scholar 

  • Chuck G, Meeley R, Irish E, Sakai H, Hake S (2007) The maize tasselseed4 microRNA controls sex determination and meristem cell fate by targeting Tasselseed6/indeterminate spikelet1. Nat Genet 3912:1517–1521

    Article  CAS  Google Scholar 

  • Chuck G, Meeley R, Hake S (2008) Floral meristem initiation and meristem cell fate are regulated by the maize AP2 genes ids1 and sid1. Development 135:3013–3019

    Article  CAS  PubMed  Google Scholar 

  • Coen ES, Meyerowitz EM (1991) The war of the whorls: genetic interactions controlling flower development. Nature 353:31–37

    Article  CAS  PubMed  Google Scholar 

  • Colombo L, Marziani G, Masiero S, Wittich PE, Schmidt RJ, Gorla MS, Pe ME (1998) BRANCHED SILKLESS mediates the transition from spikelet to floral meristem during Zea mays ear development. Plant J 16:355–363

    Article  CAS  Google Scholar 

  • Daher A, Adam H, Chabrillange N, Collin M, Mohamed N, Tregear JW, Aberlenc-Bertossi F, Rogers HJ (2010) Cell cycle arrest characterizes the transition from a bisexual floral bud to a unisexual flower in Phoenix dactylifera. Ann Bot 106:255–266

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Danilevskaya ON, Meng X, Selinger DA, Deschamps S, Hermon P, Vansant G, Gupta R, Ananiev EV, Muszynski MG (2008) Involvement of the MADS-Box gene ZMM4 in floral induction and inflorescence development in maize. Plant Physiol 147:2054–2069

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Dellaporta SL, Calderon-Urrea A (1993) Sex determination in flowering plants. Plant Cell 5:1241–1251

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Dellaporta SL, Calderon-Urrea A (1994) The sex determination process in maize. Science 266:1501–1505

    Article  CAS  PubMed  Google Scholar 

  • DeLong A, Calderon-Urrea A, Dellaporta SL (1993) Sex determination gene TASSEL SEED2 of maize encodes a short-chain alcohol dehydrogenase required for stage specific floral organ abortion. Cell 74:757–768

    Article  CAS  PubMed  Google Scholar 

  • Emerson RA (1920) Heritable characters of maize. II. Pistillate flowered maize plants. J Hered 11:65–76

    Google Scholar 

  • Emerson RA (1932) The present status of maize genetics. Congress Genetics 1:141–152

    Google Scholar 

  • Emerson RA, Emerson SE (1922) Genetic interrelations of two andromonoecious types of maize. Genetics 7:203–227

    CAS  PubMed  PubMed Central  Google Scholar 

  • Eveland AL, Jackson DP (2012) Sugars, signalling, and plant development. J Exp Bot 63:3367–3377

    Article  CAS  PubMed  Google Scholar 

  • Eveland AL, Goldshmidt A, Pautler M, Morohashi K, Liseron-Monfils C, Lewis MW, Kumari S, Hiraga S, Yang F, Unger-Wallace E, Olson A, Hake S, Vollbrecht E, Grotewold E, Ware D, Jackson D (2014) Regulatory modules controlling maize inflorescence architecture. Genome Res 24:431–443

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Favaro R, Pinyopich A, Battaglia R, Kooiker M, Borghi L, Ditta G, Yanofsky MF, Kater MM, Colombo L (2003) MADS-box protein complexes control carpel and ovule development in Arabidopsis. Plant Cell 15:2603–2611

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Ferreyra MLF, Emiliani J, Rodriguez EJ, Campos-Bermudez VA, Grotewold E, Casati P (2015) The identification of maize and Arabidopsis type I FLAVONE SYNTHASEs links flavones with hormones and biotic interactions. Plant Physiol 169:1090–1107

    Article  CAS  Google Scholar 

  • Fischer A, Baum N, Saedler H, TheiBlen G (1995) Chromosomal mapping of the MADS-box multigene family in Zea mays reveals dispersed distribution of allelic genes as well as transposed copies. Nucleic Acids Res 2311:1901–1911

    Article  Google Scholar 

  • Fraser AC (1933) Heritable characters of maize. XLIV-silky earss. J Hered 24:41–46

    Google Scholar 

  • Fujioka S, Yamane H, Spray CR, Gaskin P, Mac Millan J, Phinney BO, Takahashi N (1988) Qualitative and quantitative analyses of gibberellins in vegetative shoots of normal, dwarf-1, dwarf-2, dwarf-3, and dwarf-5 seedlings of Zea mays L. Plant Physiol 88:1367–1372

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Gallavotti A, Yan Y, Schmidt RJ, Jackson D (2008) The relationship between auxin transport and maize branching. Plant Physiol 147:1913–1923

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Gallavotti A, Long JA, Stanfield S, Yang X, Jackson D, Vollbrecht E, Schmidt RJ (2010) The control of axillary meristem fate in the maize ramosa pathway. Development 137:2849–2856

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Galli M, Liu Q, Moss BL, Malcomber S, Li W, Gaines C, Federici S, Roshkovan J, Meeley R, Nemhauser JL, Gallavotti A (2015) Auxin signaling modules regulate maize inflorescence architecture. Proc Natl Acad Sci USA 112:13372–13377

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Hake S, Ross-Ibarra J (2015) Genetic, evolutionary and plant breeding insights from the domestication of maize. Elife 4:e05861

    Article  CAS  PubMed Central  Google Scholar 

  • Hartwig T, Chuck G, Fujiokac S, Klempiena A, Weizbauera R, Potlurid DP, Choee S, Johalf G, Schulz B (2011) Brassinosteroid control of sex determination in maize. Proc Natl Acad Sci USA 108:19814–19819

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Hartwig T, Corvalan C, Best NB, Budka JS, Jia-Ying Z, Choe S, Schulz B (2012) Propiconazole is a specific and accessible Brassinosteroid (BR biosynthesis inhibitor for Arabidopsis and maize). PLoS One 7:e36625

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Heuer S, Hansen S, Bantin J, Brettschneider R, Kranz E, Lörz H, Dresselhaus T (2001) The maize MADS-box gene ZmMADS3 affects node number and spikelet development and is co-expressed with ZmMADS1 during flower development, in egg cells, and early embryogenesis. Plant Physiol 127:33–45

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Hirose N, Takei K, Kuroha T, Kamada-Nobusada T, Hayashi H, Sakakibara H (2008) Regulation of cytokinin biosynthesis, compartmentalization and translocation. J Exp Bot 591:75–83

    Google Scholar 

  • Hollick JB, Kermicle JL, Parkinson SE (2005) Rmr6 maintains meiotic inheritance of paramutant states in Zea mays. Genetics 171:725–740

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Hua Z (1998) Recent advances in mechanisms of sex differentiation in maize (Zea mays). J Agric Biotechnol 6:293–299

    Google Scholar 

  • Huang S, Cerny RE, Youlin Q, Bhat D, Aydt CM, Hanson DD, Malloy KP, Ness LA (2003) Transgenic studies on the involvement of cytokinin and gibberellin in male development. Plant Physiol 131:1270–1282

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Huq E (2006) Degradation of negative regulators: a common theme in hormone and light signaling networks? Trends Plant Sci 11:4

    Article  CAS  PubMed  Google Scholar 

  • Irish EE (1996) Regulation of sex determination in maize. BioEssays 18:363–369

    Article  Google Scholar 

  • Irish EE (1997) Class II tassel seed mutations provide evidence for multiple types of inflorescence meristems in maize (Poaceae). Am J Bot 84:1502–1515

    Article  CAS  PubMed  Google Scholar 

  • Irish EE, Langdale JA, Nelson TM (1994) Interactions between tassel seed genes and other sex determining genes in maize. Dev Genet 152:155–171

    Article  Google Scholar 

  • Jones DF (1925) Heritable characters in maize. XXIII. Silkless. J Hered 16:339–341

    Google Scholar 

  • Jones DF (1931) Dioecious maize. Science 73:432

    Article  CAS  PubMed  Google Scholar 

  • Jones DF (1934) Unisexual maize plants and their bearing on sex differentiation in other plants and in animals. Genetics 19:552–567

    CAS  PubMed  PubMed Central  Google Scholar 

  • Kempton JH (1934) Heritable characters in maize. XLVII-branched silkless. J Hered 251:29–32

    Google Scholar 

  • Kerstetter RA, Laudencia-Chingcuanco D, Smith LG, Hake S (1997) Loss-of-function mutations in the maize homeobox gene, knotted1, are defective in shoot meristem maintenance. Development 12416:3045–3054

    Google Scholar 

  • Kieffer M, Neve J, Kepinski S (2010) Defining auxin response contexts in plant development. Curr Opin Plant Biol 13:12–20

    Article  CAS  PubMed  Google Scholar 

  • Kim JC, Laparra H, Calderón-Urrea A, Mottinger JP, Moreno MA, Della-porta SL (2007) Cell cycle arrest of stamen initials in maize sex determination. Genetics 177:2547–2551

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Kobayashi K, Maekawa M, Miyao A, Hirochika H, Kyozuka J (2010) PANICLE PHYTOMER2 (PAP2), encoding a SEPALLATA subfamily MADS-box protein, positively controls spikelet meristem identity in rice. Nat Rev Genet 511:47–57

    Google Scholar 

  • Krizek BA, Fletcher JC (2005) Molecular mechanisms of flower development: an armchair guide. Nat Rev Genet 6:688–698

    Article  CAS  PubMed  Google Scholar 

  • Laudencia-Chingcuanco D, Hake S (2002) The indeterminate floral apex1 gene regulates meristem determinacy and identity in the maize inflorescence. Development 129:2629–2638

    CAS  PubMed  Google Scholar 

  • Lawit SJ, Wych HM, Deping X, Kundu S, Tomes DT (2010) Maize DELLA proteins dwarf plant8 and dwarf plant9 as modulators of plant development. Plant Cell Physiol 5111:1854–1868

    Article  CAS  Google Scholar 

  • Le Roux LG, Kellogg EA (1999) Floral development and the formation of unisexual spikelets in the Andropogoneae (Poaceae). Am J Bot 86:354–366

    Article  PubMed  Google Scholar 

  • Lenhard M, Bohnert A, Jurgens G, Laux T (2001) Termination of stem cell maintenance in Arabidopsis floral meristems by interactions between WUSCHEL and AGAMOUS. Cell 105:805–814

    Article  CAS  PubMed  Google Scholar 

  • Li N, Liu Y, Zhong M, Jiang M, Li H (2014) Thinking out of the box: MADS-box genes and maize spikelet development. Afr J Biotechnol 13:4673–4769

    Article  CAS  Google Scholar 

  • Lid SE, Meeley RB, Min Z, Nichols S, Olsen O (2004) Knock-out mutants of two members of the AGL2 subfamily of MADS-box genes expressed during maize kernel development. Plant Sci 167:575–582

    Article  CAS  Google Scholar 

  • Liu H, Qin C, Chen Z, Zuo T, Yang X, Zhou H, Xu M, Cao S, Shen Y, Lin H, He X, Zhang Y, Li L, Ding H, Thomas L, Zhang Z, Pan G (2014) Identification of miRNAs and their target genes in developing maize ears by combined small RNA and degradome sequencing. BMC Genom 15:25

    Article  CAS  Google Scholar 

  • Lohmann JU, Hong RL, Hobe M, Busch MA, Parcy F, Simon R, Weigel D (2001) A molecular link between stem cell regulation and floral patterning in Arabidopsis. Cell 105:793–803

    Article  CAS  PubMed  Google Scholar 

  • McSteen P, Laudencia-Chingcuanco D, Colasanti J (2000) A floret by any other name: control of meristem identity in maize. Trends Plant Sci 52:61–66

    Article  Google Scholar 

  • Mena M, Mandel MA, Lerner DR, Yanofsky MF, Schmidt RJ (1995) A characterization of the MADS-box gene family in maize. Plant J 8:845–854

    Article  CAS  PubMed  Google Scholar 

  • Mena M, Ambrose BA, Meeley RB, Briggs SP, Yanofsky MF, Schmidt RJ (1996) Diversification of C-function activity in maize flower development. Science 274:1537–1540

    Article  CAS  PubMed  Google Scholar 

  • Münster T, Wingen LU, Faigl W, Werth S, Saedler H, Theißen G (2001) Characterization of three GLOBOSA-like MADS-box genes from maize: evidence for ancient paralogy in one class of floral homeotic B-function genes of grasses. Gene 262:1–3

    Article  PubMed  Google Scholar 

  • Münster T, Deleu W, Wingen LU, Ouzunova M, Cacharrón J, Faigl W, Werth S, Kim JTT, Saedler H, Theissen G (2002) Maize MADS-box genes galore. Maydica 47:287–301

    Google Scholar 

  • Ng M, Yanofsky MF (2001a) Activation of the Arabidopsis B class homeotic genes by APETALA1. Plant Cell 13:739–753

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Ng M, Yanofsky MF (2001b) Function and evolution of the plant MADS-box gene family. Nat Rev Genet 2:186–195

    Article  CAS  PubMed  Google Scholar 

  • Nickerson NH (1959) Sustained treatment with gibberellin acid of five different kinds of maize. Ann Mo Bot Gard 471:19–37

    Article  Google Scholar 

  • Nickerson NH, Dale EE (1955) Tassel modifications in Zea mays. Ann Mo Bot Gard 42:195–212

    Article  Google Scholar 

  • Parenicová L, Folter S, Kieffer M, Horner DS, Favalli C, Busscher J, Cook HE, Ingram RM, Kater MM, Davies B, Angenent GC, Colombo L (2003) Molecular and phylogenetic analyses of the complete MADS-box transcription factor family in Arabidopsis: new openings to the MADS world. Plant Cell 15:1538–1551

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Parkinson SE, Gross SM, Hollick JB (2007) Maize sex determination and abaxial leaf fates are canalized by a factor that maintains repressed epigenetic states. Dev Biol 308:462–473

    Article  CAS  PubMed  Google Scholar 

  • Pelaz S, Ditta GS, Baumann E, Wisman E, Yanofsky MF (2000) B and C floral organ identity functions require SEPALLATA MADS-box genes. Nature 405:200–203

    Article  CAS  PubMed  Google Scholar 

  • Pelaz S, Gustafson-Brown C, Kohalmi SE, Crosby WL, Yanofsky MF (2001) APETALA1 and SEPALLATA3 interact to promote flower development. Plant J 26:385–394

    Article  CAS  PubMed  Google Scholar 

  • Phipps IF (1928) Heritable characters of maize XXXI. Tassel seed-4. J Hered 19:399–403

    Google Scholar 

  • Pineda RA, Brugière N, Vankova R, Malbeck J, Olson JM, Haines SC, Martin RC, Habben JE, Mok DWS, Mok MC (2008) Over-expression of a zeatin O-glucosylation gene in maize leads to growth retardation and tassel seed formation. J Exp Bot 5910:2673–2686

    Article  CAS  Google Scholar 

  • Pinyopich A, Ditta GS, Savidge B, Liljegren SJ, Baumann E, Wisman E, Yanofsky MF (2003) Assessing the redundancy of MADS-box genes during carpel and ovule development. Nature 424:85–88

    Article  CAS  PubMed  Google Scholar 

  • Rogers HJ (2006) Programmed cell death in floral organs: how and why do flowers die? Ann Bot 97:309–315

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Rood SB, Pharis RP, Major DJ (1980) Changes of endogenous gibberellin-like substances with sex reversal of the apical inflorescence of corn. Plant Physiol 66:793–796

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Sakakibara H (2006) Cytokinins: activity, biosynthesis, and translocation. Annu Rev Plant Biol 57:431–449

    Article  CAS  PubMed  Google Scholar 

  • Satoh-Nagasawa N, Nagasawa N, Malcomber S, Sakai H, Jackson D (2006) A trehalose metabolic enzyme controls inflorescence architecture in maize. Nature 441:227–230

    Article  CAS  PubMed  Google Scholar 

  • Schmidt RJ, Veit B, Mandel MA, Mena M, Hake S, Yanofsky MF (1993) Identification and molecular characterization of ZAG1, the maize homolog of the Arabidopsis floral homeotic gene AGAMOUS. Plant Cell 5:729–737

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Schreiber DN, Bantin J, Dresselhaus T (2004) The MADS box transcription factor ZmMADS2 is required for anther and pollen maturation in maize and accumulates in apoptotic bodies during anther dehiscence. Plant Physiol 134:1069–1079

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Sekimata K, Kimura T, Kaneko I, Nakano T, Yoneyama K (2001) A specific brassinosteroid biosynthesis inhibitor, Brz 2001: evaluation of its effects on Arabidopsis, cress, tobacco, and rice. Planta 213:716–721

    Article  CAS  PubMed  Google Scholar 

  • Song S, Qi T, Qia T, Huang H, Rena Q, Wua D, Changb C, Penga W, Liua Y, Pengb J, Xie D (2010) The jasmonate-ZIM domain proteins interact with the R2R3-MYB transcription factors MYB21 and MYB24 to affect jasmonate-regulated stamen development in Arabidopsis. Plant Cell 23:1000–1013

    Article  CAS  Google Scholar 

  • Spray CR, Kobayashi M, Suzki Y, Phinney BO, Gaskin P, Macmillan J (1996) The dwarf-1(d1) mutant of Zea mays blocks three steps in the gibberellin-biosynthetic pathway. Proc Natl Acad Sci USA 93:10515–10518

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Tanaka W, Pautler M, Jackson D, Hirano HY (2013) Grass meristems II: inflorescence architecture, flower development and meristem fate. Plant Cell Physiol 54:313–324

    Article  CAS  PubMed  Google Scholar 

  • Theißen G (2001) Development of floral organ identity: stories from the MADS house. Curr Opin Plant Biol 41:75–85

    Article  Google Scholar 

  • Theißen G, Saedler H (2001) Plant biology: floral quartets. Nature 409:469–471

    Article  PubMed  Google Scholar 

  • Theissen G, Strater T, Fischer A, Saedler H (1995) Structural characterization, chromosomal localization and phylogenetic evaluation of two pairs of AGAMOUS-like MADS-box genes from maize. Gene 156:155–166

    Article  CAS  PubMed  Google Scholar 

  • Theißen G, Becker A, Di Rosa A, Kanno A, Kim JT, Münster T, Winter K-U, Saedler H (2000) A short history of MADS-box genes in plants. Plant Mol Biol 42:115–149

    Article  PubMed  Google Scholar 

  • Thompson BE, Hake S (2009) Translational biology: from Arabidopsis flowers to grass inflorescence architecture. Plant Physiol 149:38–45

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Thompson BE, Bartling L, Whipple C, Hall DH, Sakai H, Schmidt R, Hakea S (2009) bearded-ear encodes a MADS box transcription factor critical for maize floral development. Plant Cell 21:2578–2590

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Veit B, Schmidt RJ, Hake S, Yanofsky MY (1993) Maize floral development: new genes and old mutants. Plant Cell 5:1205–1215

    Article  PubMed  PubMed Central  Google Scholar 

  • Vollbrecht E, Springer PS, Goh L, Buckler ES, Martienssen R (2005) Architecture of floral branch systems in maize and related grasses. Nature 436:1119–1126

    Article  CAS  PubMed  Google Scholar 

  • Wasternack C, Hause B (2013) Jasmonates: biosynthesis, perception, signal transduction and action in plant stress response, growth and development. An update to the 2007 review in Annals of Botany. Annals of Botany Weinberg: Oxford University Press, pp 1–38

  • Weige D, Meyerowitz EM (1994) The ABCs of floral homeotic gene. Cell 782:203–209

    Article  Google Scholar 

  • Whipple CJ, Ciceri P, Padilla CM, Ambrose BA, Bandong SL, Schmidt RJ (2004) Conservation of B-class floral homeotic gene function between maize and Arabidopsis. Development 13124:6083–6090

    Article  CAS  Google Scholar 

  • Winkler RG, Freeling M (1994) Physiological genetics of the dominant gibberellin-nonresponsive maize dwarfs, Dwarf8 and Dwarf9. Planta 193:341–348

    Article  CAS  Google Scholar 

  • Yamaguchi S, Kamiya Y (2000) Gibberellin biosynthesis: its regulation by endogenous and environmental signals. Plant Cell Physiol 41:251–257

    Article  CAS  PubMed  Google Scholar 

  • Yamasaki S, Fujii N, Takahashi H (2005) Hormonal regulation of sex expression in plants. Vitamins Hormones 72:79–110

    Article  CAS  PubMed  Google Scholar 

  • Yan Y, Borrego E, Kolomiets MV (2013) Jasmonate biosynthesis, perception and function in plant development and stress responses, chap 16. Lipid Metabolism. In Tech, Texas

  • Yang T, Li C (2012) Hormone regulation of sex determination in maize. Chin Bull Bot 471:65–73

    Google Scholar 

  • Young TE, Giesler-Lee J, Gallie DR (2004) Senescence-induced expression of cytokinin reverses pistil abortion during maize flower development. Plant J 38:910–922

    Article  CAS  PubMed  Google Scholar 

  • Yue R, Tie S, Sun T, Zhang L, Yang Y, Qi J, Yan S, Han X, Wang H, Shen C (2015) Genome-wide identification and expression profiling analysis of ZmPIN, ZmPILS, ZmLAX and ZmABCB auxin transporter gene families in maize (Zea mays L.) under various abiotic stresses. PLoS One 10:e0118751

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Zhang Z, Li H, Zhang D, Liu Y, Fu J, Shi Y, Song Y, Wang T, Li Y (2012) Characterization and expression analysis of six MADS-box genes in maize (Zea mays L.). J Plant Physiol 169:797–806

    Article  CAS  PubMed  Google Scholar 

  • Zhou X, Yan S, Sun C, Li S, Li J, Xu M, Liu X, Zhang S, Zhao Q, Li Y, Fan Y, Chen R, Wang L (2015) A maize jasmonate Zim-Domain protein, ZmJAZ14, associates with the JA, ABA, and GA signaling pathways in transgenic Arabidopsis. PLoS One 10:e0121824

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Zhu Y, Fu J, Zhang J, Liu T, Jia Z, Wang J, Jin Y, Lian Y, Wang M, Zheng J, Hou W, Wan J (2009) Genome-wide analysis of gene expression profiles during ear development of maize. Plant Mol Biol 70:63–77

    Article  CAS  PubMed  Google Scholar 

Download references

Acknowledgments

The author would like to acknowledge anonymous reviewers for helpful suggestions.

Author information

Authors and Affiliations

Authors

Corresponding authors

Correspondence to Qinglin Li or Baoshen Liu.

Rights and permissions

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Li, Q., Liu, B. Genetic regulation of maize flower development and sex determination. Planta 245, 1–14 (2017). https://doi.org/10.1007/s00425-016-2607-2

Download citation

  • Received:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s00425-016-2607-2

Keywords

Navigation