Literature DB >> 19386809

Expression level of ABERRANT PANICLE ORGANIZATION1 determines rice inflorescence form through control of cell proliferation in the meristem.

Kyoko Ikeda-Kawakatsu1, Naoko Yasuno, Tetsuo Oikawa, Shigeru Iida, Yasuo Nagato, Masahiko Maekawa, Junko Kyozuka.   

Abstract

Two types of branches, rachis branches (i.e. nonfloral) and spikelets (i.e. floral), are produced during rice (Oryza sativa) inflorescence development. We previously reported that the ABERRANT PANICLE ORGANIZATION1 (APO1) gene, encoding an F-box-containing protein orthologous to Arabidopsis (Arabidopsis thaliana) UNUSUAL FLORAL ORGANS, suppresses precocious conversion of rachis branch meristems to spikelets to ensure generation of certain number of spikelets. Here, we identified four dominant mutants producing an increased number of spikelets and found that they are gain-of-function alleles of APO1. The APO1 expression levels are elevated in all four mutants, suggesting that an increase of APO1 activity caused the delay in the program shift to spikelet formation. In agreement with this result, ectopic overexpression of APO1 accentuated the APO1 gain-of-function phenotypes. In the apo1-D dominant alleles, the inflorescence meristem starts to increase in size more vigorously than the wild type when switching to the reproductive development phase. This alteration in growth rate is opposite to what is observed with the apo1 mutants that have a smaller inflorescence meristem. The difference in meristem size is caused by different rates of cell proliferation. Collectively, these results suggest that the level of APO1 activity regulates the inflorescence form through control of cell proliferation in the meristem.

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Year:  2009        PMID: 19386809      PMCID: PMC2689948          DOI: 10.1104/pp.109.136739

Source DB:  PubMed          Journal:  Plant Physiol        ISSN: 0032-0889            Impact factor:   8.340


  56 in total

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Journal:  Nature       Date:  2000-04-20       Impact factor: 49.962

2.  Genomic identification of direct target genes of LEAFY.

Authors:  Dilusha A William; Yanhui Su; Michael R Smith; Meina Lu; Don A Baldwin; Doris Wagner
Journal:  Proc Natl Acad Sci U S A       Date:  2004-01-21       Impact factor: 11.205

3.  An active DNA transposon nDart causing leaf variegation and mutable dwarfism and its related elements in rice.

Authors:  Kazuo Tsugane; Masahiko Maekawa; Kyoko Takagi; Hiroyuki Takahara; Qian Qian; Chang-Ho Eun; Shigeru Iida
Journal:  Plant J       Date:  2006-01       Impact factor: 6.417

4.  Direct control of shoot meristem activity by a cytokinin-activating enzyme.

Authors:  Takashi Kurakawa; Nanae Ueda; Masahiko Maekawa; Kaoru Kobayashi; Mikiko Kojima; Yasuo Nagato; Hitoshi Sakakibara; Junko Kyozuka
Journal:  Nature       Date:  2007-02-08       Impact factor: 49.962

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Authors:  D L Hartl; H Ochman
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6.  The floral organ number4 gene encoding a putative ortholog of Arabidopsis CLAVATA3 regulates apical meristem size in rice.

Authors:  Huangwei Chu; Qian Qian; Wanqi Liang; Changsong Yin; Hexin Tan; Xuan Yao; Zheng Yuan; Jun Yang; Hai Huang; Da Luo; Hong Ma; Dabing Zhang
Journal:  Plant Physiol       Date:  2006-09-29       Impact factor: 8.340

7.  Architecture of floral branch systems in maize and related grasses.

Authors:  Erik Vollbrecht; Patricia S Springer; Lindee Goh; Edward S Buckler; Robert Martienssen
Journal:  Nature       Date:  2005-07-24       Impact factor: 49.962

8.  Partial conservation of LFY function between rice and Arabidopsis.

Authors:  Atsushi Chujo; Ze Zhang; Hirohisa Kishino; Ko Shimamoto; Junko Kyozuka
Journal:  Plant Cell Physiol       Date:  2003-12       Impact factor: 4.927

9.  Shoot meristem size is dependent on inbred background and presence of the maize homeobox gene, knotted1.

Authors:  E Vollbrecht; L Reiser; S Hake
Journal:  Development       Date:  2000-07       Impact factor: 6.868

10.  Loss-of-function mutations in the maize homeobox gene, knotted1, are defective in shoot meristem maintenance.

Authors:  R A Kerstetter; D Laudencia-Chingcuanco; L G Smith; S Hake
Journal:  Development       Date:  1997-08       Impact factor: 6.868

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  55 in total

1.  OsSPL14 promotes panicle branching and higher grain productivity in rice.

Authors:  Kotaro Miura; Mayuko Ikeda; Atsushi Matsubara; Xian-Jun Song; Midori Ito; Kenji Asano; Makoto Matsuoka; Hidemi Kitano; Motoyuki Ashikari
Journal:  Nat Genet       Date:  2010-05-23       Impact factor: 38.330

2.  Role of rice PPS in late vegetative and reproductive growth.

Authors:  Nobuhiro Tanaka; Jun-Ichi Itoh; Yasuo Nagato
Journal:  Plant Signal Behav       Date:  2012-01

3.  Overexpression of microRNA OsmiR397 improves rice yield by increasing grain size and promoting panicle branching.

Authors:  Yu-Chan Zhang; Yang Yu; Cong-Ying Wang; Ze-Yuan Li; Qing Liu; Jie Xu; Jian-You Liao; Xiao-Jing Wang; Liang-Hu Qu; Fan Chen; Peiyong Xin; Cunyu Yan; Jinfang Chu; Hong-Qing Li; Yue-Qin Chen
Journal:  Nat Biotechnol       Date:  2013-07-21       Impact factor: 54.908

4.  NAL1 allele from a rice landrace greatly increases yield in modern indica cultivars.

Authors:  Daisuke Fujita; Kurniawan Rudi Trijatmiko; Analiza Grubanzo Tagle; Maria Veronica Sapasap; Yohei Koide; Kazuhiro Sasaki; Nikolaos Tsakirpaloglou; Ritchel Bueno Gannaban; Takeshi Nishimura; Seiji Yanagihara; Yoshimichi Fukuta; Tomokazu Koshiba; Inez Hortense Slamet-Loedin; Tsutomu Ishimaru; Nobuya Kobayashi
Journal:  Proc Natl Acad Sci U S A       Date:  2013-12-02       Impact factor: 11.205

5.  A gene controlling the number of primary rachis branches also controls the vascular bundle formation and hence is responsible to increase the harvest index and grain yield in rice.

Authors:  Tomio Terao; Kenji Nagata; Kazuko Morino; Tatsuro Hirose
Journal:  Theor Appl Genet       Date:  2009-11-22       Impact factor: 5.699

6.  Phyllotaxis: from classical knowledge to molecular genetics.

Authors:  Xiaofeng Yin
Journal:  J Plant Res       Date:  2021-02-07       Impact factor: 2.629

7.  TAWAWA1, a regulator of rice inflorescence architecture, functions through the suppression of meristem phase transition.

Authors:  Akiko Yoshida; Masafumi Sasao; Naoko Yasuno; Kyoko Takagi; Yasufumi Daimon; Ruihong Chen; Ryo Yamazaki; Hiroki Tokunaga; Yoshinori Kitaguchi; Yutaka Sato; Yoshiaki Nagamura; Tomokazu Ushijima; Toshihiro Kumamaru; Shigeru Iida; Masahiko Maekawa; Junko Kyozuka
Journal:  Proc Natl Acad Sci U S A       Date:  2012-12-24       Impact factor: 11.205

8.  Rice zinc finger protein DST enhances grain production through controlling Gn1a/OsCKX2 expression.

Authors:  Shuyu Li; Bingran Zhao; Dingyang Yuan; Meijuan Duan; Qian Qian; Li Tang; Bao Wang; Xiaoqiang Liu; Jie Zhang; Jun Wang; Jiaqiang Sun; Zhao Liu; Yu-Qi Feng; Longping Yuan; Chuanyou Li
Journal:  Proc Natl Acad Sci U S A       Date:  2013-02-04       Impact factor: 11.205

9.  OsmiR396d-regulated OsGRFs function in floral organogenesis in rice through binding to their targets OsJMJ706 and OsCR4.

Authors:  Huanhuan Liu; Siyi Guo; Yunyuan Xu; Chunhua Li; Zeyong Zhang; Dajian Zhang; Shujuan Xu; Cui Zhang; Kang Chong
Journal:  Plant Physiol       Date:  2014-03-04       Impact factor: 8.340

10.  PANICLE PHYTOMER2 (PAP2), encoding a SEPALLATA subfamily MADS-box protein, positively controls spikelet meristem identity in rice.

Authors:  Kaoru Kobayashi; Masahiko Maekawa; Akio Miyao; Hirohiko Hirochika; Junko Kyozuka
Journal:  Plant Cell Physiol       Date:  2009-11-19       Impact factor: 4.927

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