Microtubule-Associated AIR9 Recognizes the Cortical Division Site at Preprophase and Cell-Plate Insertion

Current Biology

Volumn 16, Issue 19, 2006, Pages 1938-1943

  Buschmann, Henrik ^a   Chan, Jordi ^a   Sanchez Pulido, Luis ^b   Andrade Navarro, Miguel A ^c   Doonan, John H ^a   Lloyd, Clive W ^a  

^a JOHN INNES CENTRE   (United Kingdom)

^b CENTRO NACIONAL DE BIOTECNOLOGÍA   (Spain)

^c OTTAWA HOSPITAL RESEARCH INSTITUTE   (Canada)

Author keywords

CELLBIO

Indexed keywords

AIR9 PROTEIN, ARABIDOPSIS; ARABIDOPSIS PROTEIN; MICROTUBULE ASSOCIATED PROTEIN; MICROTUBULE PROTEIN;

AMINO ACID SEQUENCE; ARABIDOPSIS; ARTICLE; BIOLOGY; CELL WALL; CHEMISTRY; CYTOKINESIS; CYTOLOGY; DOWN REGULATION; GENETICS; METABOLISM; MICROTUBULE; MOLECULAR GENETICS; PHYSIOLOGY; PROTEIN TERTIARY STRUCTURE; PROTEOMICS; SEQUENCE ALIGNMENT; ULTRASTRUCTURE;

AMINO ACID SEQUENCE; ARABIDOPSIS; ARABIDOPSIS PROTEINS; CELL WALL; COMPUTATIONAL BIOLOGY; CYTOKINESIS; DOWN-REGULATION; MICROTUBULE PROTEINS; MICROTUBULE-ASSOCIATED PROTEINS; MICROTUBULES; MOLECULAR SEQUENCE DATA; PROTEIN STRUCTURE, TERTIARY; PROTEOMICS; SEQUENCE ALIGNMENT;

EMBRYOPHYTA; TRYPANOSOMATIDAE;

EID: 33749251814     PISSN: 09609822     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.cub.2006.08.028     Document Type: Article

References (24)

1. Jürgens G. Cytokinesis in higher plants. Annu. Rev. Plant Biol. 56 (2005) 281-299
2. Gunning B.E.S. The cytokinetic apparatus: Its development and spatial regulation. In: Lloyd C.W. (Ed). The Cytoskeleton in Plant Growth and Development (1982), Academic Press, New York 229-292
3. Mineyuki Y. The preprophase band of microtubules: Its function as a cytokinetic apparatus in higher plants. Int. Rev. Cytol. 187 (1999) 1-49
4. Mineyuki Y., and Gunning B.E.S. A role for preprophase bands of microtubules in maturation of new cell walls, and a general proposal on the function of preprophase band sites in cell division in higher plants. J. Cell Sci. 97 (1990) 527-537
5. Korolev A.V., Chan J., Naldrett M.J., Doonan J.H., and Lloyd C.W. Identification of a novel family of 70 kDa microtubule-associated proteins in Arabidopsis cells. Plant J. 42 (2005) 547-555
6. Neuteboom L.W., Ng J.M., Kuyper M., Clijdesdale O.R., Hooykaas P.J., and van der Zaal B.J. Isolation and characterization of cDNA clones corresponding with mRNAs that accumulate during auxin-induced lateral root formation. Plant Mol. Biol. 39 (1999) 273-287
7. Lalanne E., Michaelidis C., Moore J.M., Gagliano W., Johnson A., Patel R., Howden R., Vielle-Calzada J.P., Grossniklaus U., and Twell D. Analysis of transposon insertion mutants highlights the diversity of mechanisms underlying male progamic development in Arabidopsis. Genetics 167 (2004) 1975-1986
8. Altschul S.F., Madden T.L., Schaffer A.A., Zhang J., Zhang Z., Miller W., and Lipman D.J. Gapped BLAST and PSI-BLAST: A new generation of protein database search programs. Nucleic Acids Res. 25 (1997) 3389-3402
9. Eddy S.R. Profile hidden Markov models. Bioinformatics 14 (1998) 755-763
10. Bork P., Holm L., and Sander C. The immunoglobulin fold. Structural classification, sequence patterns and common core. J. Mol. Biol. 242 (1994) 309-320
11. Cutler S.R., and Ehrhardt D.W. Polarized cytokinesis in vacuolate cells of Arabidopsis. Proc. Natl. Acad. Sci. USA 99 (2002) 2812-2817
12. Yoneda A., and Hasezawa S. Origin of cortical microtubules organized at M/G1 interface: Recruitment of tubulin from phragmoplast to nascent microtubules. Eur. J. Cell Biol. 82 (2003) 461-471
13. Mathur J., Szabados L., Schaefer S., Grunenberg B., Lossow A., Jonas-Straube E., Schell J., Koncz C., and Koncz-Kalman Z. Gene identification with sequenced T-DNA tags generated by transformation of Arabidopsis cell suspension. Plant J. 13 (1998) 707-716
14. Clayton L., and Lloyd C.W. The relationship between the division plane and spindle geometry in Allium cells treated with CIPC and griseofulvin: An anti-tubulin study. Eur. J. Cell Biol. 34 (1984) 248-253
15. Cleary A. F-actin redistributions at the division site in living Tradescantia stomatal complexes as revealed by microinjection of rhodamine-phalloidin. Protoplasma 185 (1995) 152-165
16. Vanstraelen M., Van Damme D., De Rycke R., Mylle E., Inze D., and Geelen D. Cell cycle-dependent targeting of a kinesin at the plasma membrane demarcates the division site in plant cells. Curr. Biol. 16 (2006) 308-314
17. Cleary A.L., and Smith L.G. The Tangled1 gene is required for spatial control of cytoskeletal arrays associated with cell division during maize leaf development. Plant Cell 10 (1998) 1875-1888
18. Wada B. Experimentelle untersuchung lebender zellen in der teilung. IV. Die einwirkung des dampfgemisches von ammonia und chloroform auf die mitose bei den tradescantia-haarzellen. Cytologia (Tokyo) 10 (1939) 158-179
19. Wada B. Mechanism of mitosis based on studies of the submicroscopic structure and of the living state of the Tradescantia cell. Cytologia (Tokyo) 16 (1950) 1-26
20. Samuels A.L., Giddings Jr. T.H., and Staehelin L.A. Cytokinesis in tobacco BY-2 and root tip cells: A new model of cell-plate formation in higher plants. J. Cell Biol. 130 (1995) 1345-1357
21. Rost B., and Sander C. Combining evolutionary information and neural networks to predict protein secondary structure. Proteins 19 (1994) 55-72
22. Jones E.Y., Harlos K., Bottomley M.J., Robinson R.C., Driscoll P.C., Edwards R.M., Clements J.M., Dudgeon T.J., and Stuart D.I. Crystal structure of an integrin-binding fragment of vascular cell adhesion molecule-1 at 1.8 A resolution. Nature 373 (1995) 539-544
23. Pal L., Chakrabarti P., and Basu G. Sequence and structure patterns in proteins from an analysis of the shortest helices: Implications for helix nucleation. J. Mol. Biol. 326 (2003) 273-291
24. Freigang J., Proba K., Leder L., Diederichs K., Sonderegger P., and Welte W. The crystal structure of the ligand binding module of axonin-1/TAG-1 suggests a zipper mechanism for neural cell adhesion. Cell 101 (2000) 425-433