Literature DB >> 9522454

The division apparatus of plastids and mitochondria.

T Kuroiwa1, H Kuroiwa, A Sakai, H Takahashi, K Toda, R Itoh.   

Abstract

Mitochondria and plastids in eukaryotic cells contain distinct genomes and multiply in the cytoplasm by binary division of preexisting organelles. Mitochondrial and plastid nuclei are easily visualized as compartments in the matrix of organelles by high-resolution fluorescence microscopy and by immunoelectron microscopy using anti-DNA antibodies. Plastid and mitochondrial division can be clearly separated into two main events: division of the organelle nuclei, and then division of the rest of the organelles, the process of organellokinesis (mitochondriokinesis and plastidokinesis). The mechanical apparatus that regulates organellokinesis has remained undetermined. In 1986, the plastid-dividing apparatus (PD ring) for plastidokinesis was first identified by us in the primitive red alga Cyanidium caldarium RK-1. The PD ring is located in the cytoplasm outside the organelle envelope at the constricted isthmus of dividing organelles and has subsequently been found in all eukaryotic plants examined. We were also the first to identify the mitochondrion-dividing apparatus (MD ring) for mitochondriokinesis in the unicellular red alga Cyanidioschyzon merolae in 1993. Eukaryotic cell division is therefore controlled by at least three dividing apparata (rings), a contractile ring, an MD ring, and a PD ring, while bacterial division is controlled by a single bacterial contractile FtsZ ring. The aims of this review are to present the fine structure, process of formation, and contraction of the organelle-dividing apparatus, focusing on evolutionary conservation and diversion from the bacterial contractile ring.

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Year:  1998        PMID: 9522454     DOI: 10.1016/s0074-7696(08)60415-5

Source DB:  PubMed          Journal:  Int Rev Cytol        ISSN: 0074-7696


  67 in total

1.  Novel filaments 5 nm in diameter constitute the cytosolic ring of the plastid division apparatus.

Authors:  S Miyagishima ; M Takahara; T Kuroiwa
Journal:  Plant Cell       Date:  2001-03       Impact factor: 11.277

2.  A chloroplast protein homologous to the eubacterial topological specificity factor minE plays a role in chloroplast division.

Authors:  R Itoh; M Fujiwara; N Nagata; S Yoshida
Journal:  Plant Physiol       Date:  2001-12       Impact factor: 8.340

3.  Colocalization of plastid division proteins in the chloroplast stromal compartment establishes a new functional relationship between FtsZ1 and FtsZ2 in higher plants.

Authors:  R S McAndrew; J E Froehlich; S Vitha; K D Stokes; K W Osteryoung
Journal:  Plant Physiol       Date:  2001-12       Impact factor: 8.340

4.  Plastid division is driven by a complex mechanism that involves differential transition of the bacterial and eukaryotic division rings.

Authors:  M Takahara; T Mori; H Kuroiwa; T Higashiyama; T Kuroiwa
Journal:  Plant Cell       Date:  2001-10       Impact factor: 11.277

5.  Dynamic recruitment of dynamin for final mitochondrial severance in a primitive red alga.

Authors:  Keiji Nishida; Manabu Takahara; Shin-ya Miyagishima; Haruko Kuroiwa; Motomichi Matsuzaki; Tsuneyoshi Kuroiwa
Journal:  Proc Natl Acad Sci U S A       Date:  2003-02-03       Impact factor: 11.205

6.  ARC5, a cytosolic dynamin-like protein from plants, is part of the chloroplast division machinery.

Authors:  Hongbo Gao; Deena Kadirjan-Kalbach; John E Froehlich; Katherine W Osteryoung
Journal:  Proc Natl Acad Sci U S A       Date:  2003-03-17       Impact factor: 11.205

7.  Chloroplast biogenesis: control of plastid development, protein import, division and inheritance.

Authors:  Wataru Sakamoto; Shin-Ya Miyagishima; Paul Jarvis
Journal:  Arabidopsis Book       Date:  2008-07-22

8.  Chloramphenicol acetyltransferase-a new selectable marker in stable nuclear transformation of the red alga Cyanidioschyzon merolae.

Authors:  Maksymilian Zienkiewicz; Tomasz Krupnik; Anna Drożak; Anna Golke; Elżbieta Romanowska
Journal:  Protoplasma       Date:  2015-12-29       Impact factor: 3.356

9.  Direct evidence of active and rapid nuclear degradation triggered by vacuole rupture during programmed cell death in Zinnia.

Authors:  K Obara; H Kuriyama; H Fukuda
Journal:  Plant Physiol       Date:  2001-02       Impact factor: 8.340

10.  Two ftsH-family genes encoded in the nuclear and chloroplast genomes of the primitive red alga Cyanidioschyzon merolae.

Authors:  R Itoh; H Takano; N Ohta; S Miyagishima; H Kuroiwa; T Kuroiwa
Journal:  Plant Mol Biol       Date:  1999-10       Impact factor: 4.076

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