Plastid division coordination across a double-membraned structure

FEBS Letters

Volumn 581, Issue 11, 2007, Pages 2162-2167

  Maple, Jodi ^a   Møller, Simon Geir ^a  

^a UNIVERSITY OF STAVANGER   (Norway)

Author keywords

Coordination; Double membrane; Plastid division; Protein complex

Indexed keywords

BACTERIAL CELL; BILAYER MEMBRANE; CELL ACTIVITY; CELL DIVISION; CHLOROPLAST; COORDINATION; CYANOBACTERIUM; CYTOSOL; NONHUMAN; OUTER MEMBRANE; PLASTID; PRIORITY JOURNAL; PROTEIN ASSEMBLY; SHORT SURVEY; STROMA CELL;

CELL DIVISION; CELL MEMBRANE; EVOLUTION; PLANT PHYSIOLOGY; PLASTIDS;

BACTERIA (MICROORGANISMS); CYANOBACTERIA; EMBRYOPHYTA;

EID: 34248198352     PISSN: 00145793     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.febslet.2007.02.062     Document Type: Short Survey

References (55)

1. Tetlow I.J., Rawthorne S., Raines C., and Emes M.J. Plastid metabolic pathways. In: Møller S.G. (Ed). Plastids (2004), Blackwell Publishing Ltd., Oxford, UK 60-125
2. Juniper B.E., and Clowes F.A.L. Cytoplasmic organelles and cell growth in root caps. Nature 208 (1965) 864-865
3. Lydon R.F., and Roberson E.S. The quantitive ultrastructure of the pea shoot apex in relation to leaf initiation. Protoplasma 87 (1976) 387-402
4. Cran D.G., and Possingham J.V. Variation of plastid types in spinach. Protoplasma 74 (1972) 345-356
5. Pyke K.A., Rutherford S.M., Robertson E.J., and Leech R.M. arc6, a fertile Arabidopsis mutant with only two mesophyll cell chloroplasts. Plant Physiol. 106 (1994) 1169-1177
6. Pyke K.A., and Leech R.M. A genetic analysis of chloroplast division and expansion in Arabidopsis thaliana. Plant Physiol. 104 (1994) 201-207
7. McFadden G.I. Endosymbiosis and evolution of the plant cell. Curr. Opin. Plant. Biol. 2 (1999) 513-519
8. Gray M.W. Evolution of organellar genomes. Curr. Opin. Genet. Dev. 9 (1999) 678-687
9. Martin W., Rujan T., Richly E., Hansen A., Cornelsen S., Lins T., Leister D., Stoebe B., Hasegawa M., and Penny D. Evolutionary analysis of Arabidopsis, cyanobacterial, and chloroplast genomes reveals plastid phylogeny and thousands of cyanobacterial genes in the nucleus. Proc. Natl. Acad. Sci. USA 99 (2002) 12246-12251
10. Wakasugi T., Tsudzuki T., and Sugiura M. The genomics of land plant chloroplasts: Gene content and alteration of genomic information by RNA editing. Photosynth. Res. 70 (2001) 107-118
11. Bédard J., and Jarvis P. Recognition and envelope translocation of chloroplast preproteins. J. Exp. Bot. 56 (2005) 2287-2320
12. Osteryoung K.W., and Vierling E. Conserved cell and organelle division. Nature 376 (1995) 473-474
13. Osteryoung K.W., Stokes K.D., Rutherford S.M., Percival A.L., and Lee W.Y. Chloroplast division in higher plants requires members of two functionally divergent gene families with homology to bacterial ftsZ. Plant Cell 10 (1998) 1991-2004
14. Colletti K.S., Tattersall E.A., Pyke K.A., Froelich J.E., Stokes K.D., and Osteryoung K.W. A homologue of the bacterial cell division site-determining factor MinD mediates placement of the chloroplast division apparatus. Curr. Biol. 10 (2000) 507-516
15. Dinkins R., Reddy M.S., Leng M., and Collins G.B. Overexpression of the Arabidopsis thaliana MinD1 gene alters chloroplast size and number in transgenic tobacco plants. Planta 214 (2001) 180-188
16. Itoh R., Fujiwara M., Nagata N., and Yoshida S. A chloroplast protein homologous to the eubacterial topological specificity factor MinE plays a role in chloroplast division. Plant Phys. 27 (2001) 1644-1655
17. Maple J., Chua N.H., and Møller S.G. The topological specificity factor AtMinE1 is essential for correct plastid division site placement in Arabidopsis. Plant J. 31 (2002) 269-277
18. Reddy M.S., Dinkins R., and Collins G.B. Overexpression of the Arabidopsis thaliana MinE1 bacterial division inhibitor homologue gene alters chloroplast size and morphology in transgenic Arabidopsis and tobacco plants. Planta 215 (2002) 167-176
19. de Boer P.A.J., Crossley R.E., and Rothfield L.I. A division inhibitor and a topological specificity factor coded for by the minicell locus determine proper placement of the division septum in E. coli. Cell 56 (1989) 641-649
20. Maple J., Fujiwara M.T., Kitahata N., Lawson T., Baker N.R., Yoshida S., and Moller S.G. GIANT CHLOROPLAST 1 is essential for correct plastid division in Arabidopsis. Curr. Biol. 14 (2004) 776-781
21. Raynaud C., Cassier-Chauvat C., Perennes C., and Bergounioux C. An Arabidopsis homolog of the bacterial cell division inhibitor SulA is involved in plastid division. Plant Cell 16 (2004) 1801-1811
22. Koksharova O.A., and Wolk C.P. A novel gene that bears a DnaJ motif influences cyanobacterial cell division. J. Bac. 184 (2002) 5524-5528
23. Vitha S., Froehlich J.E., Koksharova O., Pyke K.A., van Erp H., and Osteryoung K.W. ARC6 is a J-domain plastid division protein and an evolutionary descendant of the cyanobacterial cell division protein Ftn2. Plant Cell 15 (2003) 1918-1933
24. Pyke K.A., and Leech R.M. Rapid image analysis screening procedure for identifying chloroplast number mutants in mesophyll cells of Arabidopsis thaliana (L.) Heynh. Plant Physiol. 96 (1991) 1193-1195
25. Shimada H., Koiyumi M., Kuroki K., Mochiyuki M., Fujimoto H., Ohta H., Masuda T., and Takamiya K.-i. ARC3, a chloroplast division factor, is a chimera of prokaryotic FtsZ and part of Eukaryotic phosphatidylinositol-4-phosphate 5-kinase. Plant Cell Physiol. 45 (2004) 960-967
26. Gao H., Kadirjan-kalbach D., Froehlich J.E., and Osteryoung K.W. ARC5, a cytosolic dynamin-like protein from plants, is part of the chloroplast division machinery. Proc. Natl. Acad. Sci. USA 100 (2003) 4328-4333
27. Miyagishima S., Froehlich J.E., and Osteryoung K.W. PDV1 and PDV2 mediate recruitment of the dynamin-related protein ARC5 to the plastid division site. Plant Cell 18 (2006) 2517-2530
28. Mita T., Kanbe T., Tanaka K., and Kuroiwa T. A ring structure around the dividing plane of the Cyanidium caldarium chloroplast. Protoplasma 130 (1986) 211-213
29. Hashimoto H. Double ring structure around the constricting neck of the dividing plastids of Avena sativa. Protoplasma 135 (1986) 166-172
30. Osteryoung K.W., and McAndrew R.S. The plastid division machine. Annu. Rev. Plant Physiol. Plant Mol. Biol. 52 (2001) 315-333
31. Stokes K.D., McAndrew R.S., Figueroa R., Vitha S., and Osteryoung K.W. Chloroplast division and morphology are differentially affected by overexpression of FtsZ1 and FtsZ2 genes in Arabidopsis. Plant Physiol. 124 (2000) 1668-1677
32. Erickson H.P., Taylor D.W., Taylor K.A., and Bramhill D. Bacterial cell division protein FtsZ assembles into protofilament sheets and minirings, structural homologs of tubulin polymers. Proc. Natl. Acad. Sci. USA 93 (1996) 519-523
33. Maple J., Aldrige C., and Møller S.G. Plastid division is mediate by combinatorial assembly of plastid division proteins. Plant J. 43 (2005) 811-823
34. de Boer P.A.J., Crossley R.E., and Rothfield L.I. The essential bacterial cell-division protein FtsZ is a GTPase. Nature 359 (1992) 254-256
35. RayChaudhuri D., and Park J.T. Escherichia coli cell-division gene ftsZ encodes a novel GTP-binding protein. Nature 359 (1992) 251-254
36. Löwe J., and Amos L.A. Crystal structure of the bacterial cell-division protein FtsZ. Nature 391 (1998) 203-206
37. Wang X., Huang J., Mukherjee A., Cao C., and Lutkenhaus J. Analysis of the interaction of FtsZ with itself, GTP, and FtsA. J. Bac. 179 (1997) 5551-5559
38. Osawa H., and Erickson H.P. FtsZ from divergent foreign bacteria can function for cell division in Escherichia coli. J. Bac. 188 (2006) 7132-7140
39. Ma S., and Margolin W. Genetic and functional analyses of the conserved C-terminal core domain of Escherichia coli FtsZ. J. Bac. 181 (1999) 7531-7544
40. El-Kafafi E.S., Mukherjee S., El-Shami M., Putaux J.L., Block M.A., Pignot-Paintrand I., Lerbs-Mache S., and Falconet D. The plastid division proteins, FtsZ1 and FtsZ2: differ in their biochemical properties and sub-plastidial localisation. Biochem. J. 387 (2005) 669-676
41. Liu Z., Mukherjee A., and Lutkenhaus J. Recruitment of ZipA to the division site by interaction with FtsZ. Mol. Micro. 31 (1999) 1853-1861
42. Maple J., Vojta L., Soll J., and Møller S.G. ARC3 is a stromal Z-ring accessory protein essential for plastid division. EMBO Rep. 8 (2007) 293-299
43. Mazouni K., Domain F., Cassier-Chauvat C., and Chauvat F. Molecular analysis of the key cytokinetic components of cyanobacteria: FtsZ, ZipN and MinCDE. Mol. Microbiol. 52 (2004) 1145-1158
44. Bukau B., and Horwich AL. The Hsp70 and Hsp60 chaperone machines. Cell 92 (1998) 351-366
45. Uehara T., Matsuzawa H., and Nishimura A. HscA is involved in the dynamics of FtsZ-ring formation in Escherichia coli K12. Genes Cells 6 (2001) 803-814
46. Raynaud C., Perennes C., Reuzeau C., Catrice O., Brown S., and Bergounioux C. Cell and plastid division are coordinated through the prereplication factor AtCDT1. Proc. Natl. Acad. Sci. USA 102 (2005) 8216-8221
47. Margolin W. Themes and variations in prokaryotic cell division. FEMS Microbiol. Rev. 24 (2000) 531-548
48. Miyagishima S., Takahara M., and Kuroiwa T. Novel filaments 5 nm in diameter constitute the cytosolic ring of the plastid division apparatus. Plant Cell 13 (2001) 707-721
49. Miyagishima S., Takahara M., Mori T., Kuroiwa H., Higashiyama T., and Kuroiwa T. Plastid division is driven by a complex mechanism that involves differential transition of the bacterial and eukaryotic division rings. Plant Cell 13 (2001) 2257-2268
50. Danino D., and Hinshaw J.E. Dynamin family of mechanoenzymes. Curr. Opin. Cell Biol. 13 (2001) 454-460
51. Lemmon M.A., and Ferguson K.M. Signal-dependent membrane targeting by pleckstrin homology (PH) domains. Biochem. J. 350 (2000) 1-18
52. Chen H., and Chan D.C. Emerging functions of mammalian mitochondrial fusion and fission. Hum. Mol. Genet. 14 (2005) R283-R289
53. Miyagishima S., Nishida K., Mori T., Matsuzaki M., Higashiyama T., Kuroiwa H., and Kuroiwa T. A plant-specific dynamin-related protein forms a ring at the chloroplast division site. Plant Cell 15 (2003) 655-665
54. Hong Z., Bednarek S.Y., Blumwald E., Hwang I., Jurgens G., Menzel D., Osteryoung K.W., Raikhel N.V., Shinozaki K., Tsutsumi N., and Verma D.P. A unified nomenclature for Arabidopsis dynamin-related large GTPases based on homology and possible functions. Plant Mol. Biol. 53 (2003) 261-265
55. Yoshida Y., Kuroiwa H., Misumi O., Nishida K., Yagisawa F., Fujiwara T., Nanamiya H., Kawamura F., and Kuroiwa T. Isolated chloroplast division machinery can actively constrict after stretching. Science 313 (2006) 1435-1438