Acta Agron Sin ›› 2012, Vol. 38 ›› Issue (11): 2034-2041.doi: 10.3724/SP.J.1006.2012.02034
• CROP GENETICS & BREEDING · GERMPLASM RESOURCES · MOLECULAR GENETICS • Previous Articles Next Articles
QIAO Lin-Yi1,**,ZHANG Lei1,**,ZHANG Wen-Ping1,ZHAO Guang-Yao2,WANG Xi1,*,JIA Ji-Zeng2,*
| [1]Vanneste S, Friml J. Auxin: a trigger for change in plant development. Cell, 2009, 136: 1005–1016[2]Dharmasiri N, Dharmasiri S, Estelle M. The F-box protein TIR1 is an auxin receptor. Nature, 2005, 435: 441–445[3]Kepinski S, Leyser O. The Arabidopsis F-box protein TIR1 is an auxin receptor. Nature, 2005, 435: 446-451[4]Jurado S, Abraham Z, Manzano C, Lopez-Torrejon G, Pacios L F, Del Pozo J C. The Arabidopsis cell cycle F box protein SKP2A binds to auxin. Plant Cell, 2010, 22: 3891–3904[5]Renate D, Hartwig L, Bianka S. ABP1, an auxin receptor for fast responses at the plasma membrane. Plant Signaling & Behavior, 2010, 5: 1–3[6]Hertel R, Thomson K S, Russo V E A. In-vitro auxin binding to particulate cell fractions from corn coleoptiles. Planta, 1972, 107: 325–340[7]Tillmann U, Viola G, Kayser B, Siemeister G, Hesse T, Palme K, Lobler M, Klambt D. cDNA clones of the auxin-binding protein from corn coleoptiles (Zea mays L.): isolation and characterization by immunological methods. EMBO J, 1989, 8: 2463–2467[8]David K M, Couch D, Braun N, Brown S, Grosclaude J, Perrot-Rechenmann C. The auxin-binding protein 1 is essential for the control of cell cycle. Plant J, 2007, 50: 197–206[9]Braun N, Wyrzykowska J, Muller P, David K, Couch D, Perrot-Rechenmann C, Fleming A J. Conditional repression of AUXIN BINDING PROTEIN1 reveals that it coordinates cell division and cell expansion during postembryonic shoot development in Arabidopsis and tobacco. Plant Cell, 2008, 20: 2746–2762[10]Perrot-Rechenmann C. Cellular responses to auxin: division versus expansion. Cold Spring Harbor Perspective in Biology, 2010, 2: a001446[11]Xu T, Wen M, Nagawa S, Fu Y, Chen J G, Wu M J, Perrot-Rechenmann C, Friml J, Jones A M, Yang Z. Cell surface- and rho GTPase-based auxin signaling controls cellular interdigitation in Arabidopsis. Cell, 2010, 143: 99–110[12]Robert S, Kleine-Vehn J, Barbez E, Sauer M, Paciorek T, Baster P, Vanneste S, Zhang J, Simon S, ?ovanová M, Hayashi K, Dhonukshe P, Yang Z B, Bednarek S Y, Jones A M, Luschnig C, Aniento F, Za?ímalová E, Friml J. ABP1 mediates auxin inhibition of clathrin-dependent endocytosis in Arabidopsis. Cell, 2010, 143: 111–121[13]Paciorek T, Zaz?malova E, Ruthardt N, Petrasek J, Stierhof Y D, Kleine-Vehn J, Morris D A, Emans N, Jurgens G, Geldner N, Friml J. Auxin inhibits endocytosis and promotes its own ef?ux from cells. Nature, 2005, 435: 1251–1256[14]Choi S Y. Molecular cloning and expression of the hot pepper ERabp1 gene encoding auxin-binding protein. Plant Mol Biol, 1996, 32: 995–997[15]Huang Y(黄妤), Liu F(刘峰), Guo Q-Q(郭清泉), Zhang X-W(张学文). Cloning and expression of auxin-binding proteins 1 gene in ramie [Boehmeria nivea (Linn.) Gaud.]. Acta Agron Sin (作物学报), 2008, 34(8): 1358–1365 (in Chinese with English abstract)[16]Devos K M, Gale M D. The use of random amplified polymorphic DNA marker in wheat. Theor Appl Genet, 1992, 84: 567–572[17]Gai J-Y(盖钧镒). Method for Experimental Statistics (试验统计方法). Beijing: China Agriculture Press, 2000. pp 90–91 (in Chinese)[18]Cechin A L, Sinigaglia M, Lemke N, Echeverrigaray S, Cabrera O G, Pereira G, Mombach J. Cupin: a candidate molecular structure for the Nep1-like protein family. London: BioMed Central Ltd., 2008 [2012-03-10]. http://www.biomedcentral.com/1471-2229/8/50[19]Wang B(王冰), Li J-Y(李家洋), Wang Y-H(王永红). Advances in understanding the roles of auxin involved in modulating plant architecture. Chin Bull Bot (植物学通报), 2006, 23(5): 443–458 (in Chinese with English abstract)[20]Friml J, Benkova E, Blilou I, Wisniewska J, Hamann T, Ljung K, Woody S, Sandberg G, Scheres B, Jurgens G, Palme K. AtPIN4 mediates sink-driven auxin gradients and root patterning in Arabidopsis. Cell, 2002, 108: 661–673[21]Benjamins R, Scheres B. Auxin: the looping star in plant development. Annu Rev Plant Biol, 2008, 59: 443–465[22]Li Y C, Korol A B, Fahim T, Nevo E. Microsatellites within genes: structure, function, and evolution. Mol Biol Evol, 2004, 21: 991–1007[23]Chapman M A, Pashley C H, Wenzler J, Hvala J, Tang S X, Knapp S J, Burkea J M. A genomic scan for selection reveals candidates for genes involved in the evolution of cultivated sunflower (Helianthus annuus). Plant Cell, 2008, 20: 2931–2945[24]Hao C-Y(郝晨阳), Dong Y-C(董玉琛), Wang L-F(王兰芬), You G-X(游光霞), Zhang H-N(张洪娜), Ge H-M(葛红梅), Jia J-Z(贾继增), Zhang X-Y(张学勇). Construction and genetic diversity analysis of common wheat core collection in China. Chin Sci Bull (科学通报), 2008, 53(8): 908–915 (in Chinese without English abstract)[25]Dong Y-C(董玉琛), Cao Y-S(曹永生), Zhang X-Y(张学勇), Liu S-C(刘三才), Wang L-F(王兰芬), You G-X(游光霞), Pang B-S(庞斌双), Li L-H(李立会), Jia J-Z(贾继增). Development of candidate core collections in Chinese common wheat germplasm. J Plant Gene Resour (植物遗传资源学报), 2003, 4(1): 1–8 (in Chinese with English abstract)[26]Vigouroux Y, Mitchell S, Matsuoka Y, Hamblin M, Kresovich S, Smith S, Jaqueth J, Smith O, Doebley J. An analysis of genetic diversity across the maize genome using microsatellites. Genetics, 2005, 169:1617–1630[27]Asano K, Yamasaki M, Takuno S, Miura K, Katagiri S, Ito K, Doi K, Wu J Z, Ebana K, Matsumoto T, Innan H, Kitano H, Ashikari M, Matsuoka M. Artificial selection for a green revolution gene during japonica rice domestication. Proc Natl Acad Sci USA, 2011, 108: 11034–11039[28]Effendi Y, Rietz S, Fischer U, Scherer G F E. The heterozygous abp1/ABP1 insertional mutant has defects in functions requiring polar auxin transport and in regulation of early auxin-regulated genes. Plant J, 2011, 65: 282–294 |
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