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W. Verelst, H. Saedler, T. Münster (2007a)
MIKC* MADS‐protein complexes bind motifs enriched in the proximal region of late pollen‐specific Arabidopsis promoters, 143
L. Yin, Y. Verhertbruggen, A. Oikawa, C. Manisseri, B. Knierim, L. Prak (2011)
The cooperative activities of CSLD2, CSLD3, and CSLD5 are required for normal Arabidopsis development, 4
B.J. Adamczyk, D.E. Fernandez (2009)
MIKC* MADS domain heterodimers are required for pollen maturation and tube growth in Arabidopsis, 149
S.J. Clough, A.F. Bent (1998)
Floral dip: a simplified method for Agrobacterium‐mediated transformation of Arabidopsis thaliana, 16
M.D. Lazzaro, J.M. Donohue, F.M. Soodavar (2003)
Disruption of cellulose synthesis by isoxaben causes tip swelling and disorganizes cortical microtubules in elongating conifer pollen tubes, 220
C.M. Kim, S.H. Park, B.I. Je, S.H. Park, S.J. Park, H.L. Piao (2007)
OsCSLD1, a cellulose synthase‐like D1 gene, is required for root hair morphogenesis in rice, 143
S.C. Fang, D.E. Fernandez (2002)
Effect of regulated overexpression of the MADS domain factor AGL15 on flower senescence and fruit maturation, 130
B. Favery, E. Ryan, J. Foreman, P. Linstead, K. Boudonck, M. Steer (2001)
KOJAK encodes a cellulose synthase‐like protein required for root hair cell morphogenesis in Arabidopsis, 15
D. Meng, Z. Gu, W. Li, A. Wang, H. Yuan, Q. Yang (2014)
Apple MdABCF assists in the transportation of S‐RNase into pollen tubes, 78
D. Winter, B. Vinegar, H. Nahal, R. Ammar, G.V. Wilson, N.J. Provart (2007)
An “Electronic Fluorescent Pictograph” browser for exploring and analyzing large‐scale biological data sets, 2
S. Gepstein, G. Sabehi, M.J. Carp, T. Hajouj, M.F. Nesher, I. Yariv (2003)
Large‐scale identification of leaf senescence‐associated genes, 36
W. Wang, L. Wang, C. Chen, G. Xiong, X.Y. Tan, K.Z. Yang (2011)
Arabidopsis CSLD1 and CSLD4 are required for cellulose deposition and normal growth of pollen tubes, 62
R. Wang, M. Ming, J. Li, D. Shi, X. Qiao, L. Li (2017)
Genome‐wide identification of the MADS‐box transcription factor family in pear (Pyrus bretschneideri) reveals evolution and functional divergence, 5
S. Folter, J. Busscher, L. Colombo, A. Losa, G.C. Angenent (2004)
Transcript profiling of transcription factor genes during silique development in Arabidopsis, 56
L.C. Boavida, B. Shuai, H.J. Yu, G.C. Pagnussat, V. Sundaresan, S. McCormick (2009)
A collection of Ds insertional mutants associated with defects in male gametophyte development and function in Arabidopsis thaliana, 181
X. Qi, S. Hu, H. Zhou, X. Liu, L. Wang, B. Zhao (2018)
A MADS‐box transcription factor of ‘Kuerlexiangli’ (Pyrus sinkiangensis Yu) PsJOINTLESS gene functions in floral organ abscission, 642
Y. Mizuta, T. Higashiyama (2014)
Antisense gene inhibition by phosphorothioate antisense oligonucleotide in Arabidopsis pollen tubes, 78
C.M. Yoo, L. Quan, E.B. Blancaflor (2012)
Divergence and redundancy in CSLD2 and CSLD3 function during Arabidopsis thaliana root hair and female gametophyte development, 3
J. Yang, G. Bak, T. Burgin, W.J. Barnes, H.B. Mayes, M.J. Peña (2020)
Biochemical and genetic analysis identify CSLD3 as a beta‐1,4‐glucan synthase that functions during plant cell wall synthesis, 32
A.J. Bernal, C.M. Yoo, M. Mutwil, J.K. Jensen, G. Hou, C. Blaukopf (2008)
Functional analysis of the cellulose synthase‐like genes CSLD1, CSLD2, and CSLD4 in tip‐growing Arabidopsis cells, 148
V.A. Huynh‐Thu, A. Irrthum, L. Wehenkel, P. Geurts (2010)
Inferring regulatory networks from expression data using tree‐based methods, 5
D. Twell, J. Yamaguchi, S. McCormick (1990)
Pollen‐specific gene expression in transgenic plants: coordinate regulation of two different tomato gene promoters during microsporogenesis, 109
J.Z. Wu, Y. Lin, X.L. Zhang, D.W. Pang, J. Zhao (2008)
IAA stimulates pollen tube growth and mediates the modification of its wall composition and structure in Torenia fournieri, 59
B. Zhang, Y. Gao, L. Zhang, Y. Zhou (2021)
The plant cell wall: biosynthesis, construction, and functions, 63
Y. Chebli, M. Kaneda, R. Zerzour, A. Geitmann (2012)
The cell wall of the Arabidopsis pollen tube—spatial distribution, recycling, and network formation of polysaccharides, 160
A.K. Broz, P.A. Bedinger (2021)
Pollen–pistil interactions as reproductive barriers, 72
J. Wu, Z. Wang, Z. Shi, S. Zhang, R. Ming, S. Zhu (2013)
The genome of the pear (Pyrus bretschneideri Rehd.), 23
H. Thomas (2013)
Senescence, ageing and death of the whole plant, 197
Y. Gao, H. Zhou, J. Chen, X. Jiang, S. Tao, J. Wu (2015)
Mitochondrial dysfunction mediated by cytoplasmic acidification results in pollen tube growth cessation in Pyrus pyrifolia, 153
A. Moutinho, P.J. Hussey, A.J. Trewavas, R. Malhó (2001)
cAMP acts as a second messenger in pollen tube growth and reorientation, 98
D.M. Updegraff (1969)
Semimicro determination of cellulose in biological materials, 32
T. Arioli, L. Peng, A.S. Betzner, J. Burn, W. Wittke, W. Herth (1998)
Molecular analysis of cellulose biosynthesis in Arabidopsis, 279
G. Daras, D. Templalexis, F. Avgeri, D. Tsitsekian, K. Karamanou, S. Rigas (2021)
Updating insights into the catalytic domain properties of plant cellulose synthase (CesA) and cellulose synthase‐like (Csl) proteins, 26
M.S. Doblin, L. De Melis, E. Newbigin, A. Bacic, S.M. Read (2001)
Pollen tubes of Nicotiana alata express two genes from different beta‐glucan synthase families, 125
K.J. Livak, T.D. Schmittgen (2001)
Analysis of relative gene expression data using real‐time quantitative PCR and the 2(−Delta Delta C(T)) method, 25
W. Verelst, D. Twell, S. Folter, R. Immink, H. Saedler, T. Münster (2007b)
MADS‐complexes regulate transcriptome dynamics during pollen maturation, 8
V. Davì, H. Tanimoto, D. Ershov, A. Haupt, H. De Belly, R. Le Borgne (2018)
Mechanosensation dynamically coordinates polar growth and cell wall assembly to promote cell survival, 45
S.P. Hazen, J.S. Scott‐Craig, J.D. Walton (2002)
Cellulose synthase‐like genes of rice, 128
M. Tadege, C. Kuhlemeier (1997)
Aerobic fermentation during tobacco pollen development, 35
T.A. Richmond, C.R. Somerville (2000)
The cellulose synthase superfamily, 124
C. Chen, H. Chen, Y. Zhang, H.R. Thomas, M.H. Frank, Y. He (2020)
TBtools: an integrative toolkit developed for interactive analyses of big biological data, 13
S. Kaur, K.S. Dhugga, R. Beech, J. Singh (2017)
Genome‐wide analysis of the cellulose synthase‐like (Csl) gene family in bread wheat (Triticum aestivum L.), 17
L. Parenicová, S. Folter, M. Kieffer, D.S. Horner, C. Favalli, J. Busscher (2003)
Molecular and phylogenetic analyses of the complete MADS‐box transcription factor family in Arabidopsis: new openings to the MADS world, 15
J. Guo, Z. Yang (2020)
Exocytosis and endocytosis: coordinating and fine‐tuning the polar tip growth domain in pollen tubes, 71
J. Chen, P. Wang, B. Graaf, H. Zhang, H. Jiao, C. Tang (2018)
Phosphatidic acid counteracts S‐RNase signaling in pollen by stabilizing the actin cytoskeleton, 30
N.G. Taylor (2008)
Cellulose biosynthesis and deposition in higher plants, 178
H. Zhou, H. Yin, J. Chen, X. Liu, Y. Gao, J. Wu (2016)
Gene‐expression profile of developing pollen tube of Pyrus bretschneideri, 20
M. Bosch, P.K. Hepler (2005)
Pectin methylesterases and pectin dynamics in pollen tubes, 17
C. Wang, G. Xu, X. Jiang, G. Chen, J. Wu, H. Wu (2009)
S‐RNase triggers mitochondrial alteration and DNA degradation in the incompatible pollen tube of Pyrus pyrifolia in vitro, 57
C. Ferguson, T.T. Teeri, M. Siika‐Aho, S.M. Read, A. Bacic (1998)
Location of cellulose and callose in pollen tubes and grains of Nicotiana tabacum, 206
C. Tang, X. Zhu, X. Qiao, H. Gao, Q. Li, P. Wang (2020)
Characterization of the pectin methyl‐esterase gene family and its function in controlling pollen tube growth in pear (Pyrus bretschneideri), 112
C. Ellis, I. Karafyllidis, C. Wasternack, J.G. Turner (2002)
The Arabidopsis mutant cev1 links cell wall signaling to jasmonate and ethylene responses, 14
M.W. Steer, J.M. Steer (1989)
Pollen tube tip growth, 111
S. Robatzek, I.E. Somssich (2002)
Targets of AtWRKY6 regulation during plant senescence and pathogen defense, 16
A. Geitmann, M. Steer (2006)
The pollen tube: a cellular and molecular perspective
Cellulose, a key component of the cell wall, plays an important role in maintaining the growth of pollen tubes. However, the molecular mechanism of cellulose participating in the cessation of pear pollen tube growth remains unclear. Here, we reported that at 15 h post‐cultured (HPC), the slow‐growth pear pollen tubes showed thickened cell walls and cellulose accumulation in the inner wall. Transcriptome data and quantitative real‐time PCR analysis showed that PbrCSLD5, a cellulose synthesis‐like gene, was highly expressed in the 15 HPC pear pollen tubes. Knockdown of PbrCSLD5 caused a decrease in cellulose content in pear pollen tubes. Moreover, PbrCSLD5 overexpression in Arabidopsis resulted in the accumulation of cellulose and disruption of normal pollen tube growth. Transcription factor PbrMADS52 was found to bind to the promoter of PbrCSLD5 and enhanced its expression. Our results suggested that the PbrMADS52–PbrCSLD5 signaling pathway led to increased cellulose content in the pear pollen tube cell wall, thereby inhibiting pollen tube growth. These results provided new insights into the regulation of pollen tube growth.
Physiologia Plantarum – Wiley
Published: May 1, 2022
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