Formation and function of phragmoplast during successive cytokinesis stages in higher plant meiosis

2007 ◽  
Vol 31 (6) ◽  
pp. 626-635 ◽  
Author(s):  
N SHAMINA ◽  
E GORDEEVA ◽  
N KOVALEVA ◽  
E SERIUKOVA ◽  
N DOROGOVA
1983 ◽  
Vol 96 (2) ◽  
pp. 527-540 ◽  
Author(s):  
J Molè-Bajer ◽  
A S Bajer

We have studied the effect of taxol on mitosis in Haemanthus endosperm. Immuno-Gold Stain (IGS), a new immunocytochemical method (17), was used to visualize microtubules (MTs) in the light microscope. Observations on MT arrangements were correlated with studies in vivo. Chromosome movements are affected in all stages of mitosis which progresses over at least 10(4) range of taxol concentrations. The three most characteristic effects on MTs are: (a) enhancement of the lateral associations between MTs, seen especially during the reorganization of the polar region of the spindle, (b) promotion of MT assembly, leading to the formation of additional MTs in the spindle and MT arrays in the cytoplasm, and (c) an increase in MT stability, demonstrated in their increased cold resistance. In this report, the emphasis is on the primary, immediate effects, occurring in the first 30 min of taxol action. Effects are detected after a few mins, are reversible, and are concentration/time dependent. The spindle and phragmoplast are remarkably modified due to the enhancement of lateral associations of MTs and the formation of abundant nonkinetochore and polar, asterlike MTs. The equatorial region of the interzone in anaphase may be entirely depleted of MTs, and the spindle may break perpendicular to the spindle axis. Mitosis is completed in these conditions, providing evidence for the motile autonomy of each half-spindle. Trailing chromosome arms in anaphase are often stretched and broken. Chromosome fragments are transported away from the polar regions, i.e., in the direction opposite to that expected (5, 6). This supplies the first direct evidence of pushing by elongating MTs in an anastral higher plant spindle. These observations draw attention to the relation between the lateral association of MT ends to assembly/disassembly and to the role of such an interaction in spindle function and organization.


1994 ◽  
Vol 14 (9) ◽  
pp. 6180-6186
Author(s):  
W Sakamoto ◽  
N R Sturm ◽  
K L Kindle ◽  
D B Stern

Complex processing of primary transcripts occurs during the expression of higher-plant chloroplast genes. In Chlamydomonas reinhardtii, most chloroplast genes appear to possess their own promoters, rather than being transcribed as part of multicistronic operons. By generating specific deletion mutants, we show that petD, which encodes subunit IV of the cytochrome b6/f complex, has an RNA processing site that is required for accumulation of monocistronic petD mRNA in petD promoter deletion mutants; in such mutants, transcription of petD originates from the upstream petA promoter. The 5' ends of transcripts initiated at the petD promoter are probably also generated by processing, since the 5' end of monocistronic petD mRNA is the same in wild-type strains as it is in the petD promoter mutants. The location and function of the processing site were further examined by inserting petD-uidA fusion genes into the chloroplast genome (uidA is an Escherichia coli gene that encodes beta-glucuronidase). When a promoterless petD-uidA fusion gene was inserted downstream of petA, a monocistronic uidA transcript accumulated, which was apparently initiated at the petA promoter and was processed at a site corresponding precisely to the petD mRNA 5' end. When a construct including only sequences downstream of +25 relative to the mature mRNA 5' end was inserted into the same site, a dicistronic petA-uidA transcript accumulated but no monocistronic uidA transcript could be detected, suggesting that a processing site lies at least partially within the region from -1 to +25. Beta-glucuronidase activity was not detected in transformants that accumulated only the dicistronic petA-uidA transcript, suggesting that the first 25 bp of the 5' untranslated region are required for translation initiation. One explanation for this translational defect is that Chlamydomonas chloroplasts cannot translate the second coding region of some dicistronic messages.


2006 ◽  
Vol 18 (11) ◽  
pp. 3106-3120 ◽  
Author(s):  
László Kovács ◽  
Jakob Damkjær ◽  
Sami Kereïche ◽  
Cristian Ilioaia ◽  
Alexander V. Ruban ◽  
...  

2018 ◽  
pp. 191-227
Author(s):  
Nicola Y. Roberts ◽  
Kim Osman ◽  
F. Chris H. Franklin ◽  
Monica Pradillo ◽  
Javier Varas ◽  
...  

1994 ◽  
Vol 14 (9) ◽  
pp. 6180-6186 ◽  
Author(s):  
W Sakamoto ◽  
N R Sturm ◽  
K L Kindle ◽  
D B Stern

Complex processing of primary transcripts occurs during the expression of higher-plant chloroplast genes. In Chlamydomonas reinhardtii, most chloroplast genes appear to possess their own promoters, rather than being transcribed as part of multicistronic operons. By generating specific deletion mutants, we show that petD, which encodes subunit IV of the cytochrome b6/f complex, has an RNA processing site that is required for accumulation of monocistronic petD mRNA in petD promoter deletion mutants; in such mutants, transcription of petD originates from the upstream petA promoter. The 5' ends of transcripts initiated at the petD promoter are probably also generated by processing, since the 5' end of monocistronic petD mRNA is the same in wild-type strains as it is in the petD promoter mutants. The location and function of the processing site were further examined by inserting petD-uidA fusion genes into the chloroplast genome (uidA is an Escherichia coli gene that encodes beta-glucuronidase). When a promoterless petD-uidA fusion gene was inserted downstream of petA, a monocistronic uidA transcript accumulated, which was apparently initiated at the petA promoter and was processed at a site corresponding precisely to the petD mRNA 5' end. When a construct including only sequences downstream of +25 relative to the mature mRNA 5' end was inserted into the same site, a dicistronic petA-uidA transcript accumulated but no monocistronic uidA transcript could be detected, suggesting that a processing site lies at least partially within the region from -1 to +25. Beta-glucuronidase activity was not detected in transformants that accumulated only the dicistronic petA-uidA transcript, suggesting that the first 25 bp of the 5' untranslated region are required for translation initiation. One explanation for this translational defect is that Chlamydomonas chloroplasts cannot translate the second coding region of some dicistronic messages.


Author(s):  
R. Malcolm Brown

It is the general belief of many investigators that the pathway of cellulose biogenesis occurs via soluble pools of hexose phosphate monomers and the plasma membrane which is thought to be the site of polymerization and/or crystalization. Brown and coworkers and Ray (see 1) have proposed to the contrary that the Golgi apparatus is the site of cellulose biogenesis in certain scale-producing algae and higher plants respectively. While it has been fairly well established that cellulose can be biosynthesized by the Golgi apparatus, considerable doubt has been expressed that this type of system could be applicable to cellulose biogenesis in higher plant systems. Conversely, the problems associated with in vitro cellulose biosynthesis in Golgi-enriched homogenates raises questions about the in vivo localization of B-(1,4)-glucan synthetase activity.


1998 ◽  
Vol 75 (2) ◽  
pp. 198-209 ◽  
Author(s):  
Hwa Dai ◽  
Yih-Shan Lo ◽  
Wann-Neng Jane ◽  
Li-Wen Lee ◽  
Kwen-Sheng Chiang

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