1989
DOI: 10.1007/bf01354234
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A cytokinin-sensitive mutant of the moss,Physcomitrella patens, defective in chloroplast division

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Cited by 65 publications
(33 citation statements)
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“…Therefore, Pphb7 induction by BA is likely caused by increase of rhizoid initials accompanying adventitious bud formation. While exogenous cytokinin induces chloroplast division in protonemata (Abel et al, 1989), the numbers of plastids in wild-type and Pphb7-disrupted rhizoids treated with 10-µM BA for 48 hours were similar to that in non-treated rhizoids (data not shown). This implies that the regulation of plastid division in rhizoids differs from that in protonemata.…”
Section: Auxin and Pphb7 Function In Rhizoid Cell Differentiationmentioning
confidence: 71%
“…Therefore, Pphb7 induction by BA is likely caused by increase of rhizoid initials accompanying adventitious bud formation. While exogenous cytokinin induces chloroplast division in protonemata (Abel et al, 1989), the numbers of plastids in wild-type and Pphb7-disrupted rhizoids treated with 10-µM BA for 48 hours were similar to that in non-treated rhizoids (data not shown). This implies that the regulation of plastid division in rhizoids differs from that in protonemata.…”
Section: Auxin and Pphb7 Function In Rhizoid Cell Differentiationmentioning
confidence: 71%
“…Previously isolated P. patens mutants, BAR, PC22, and P24, exhibited a reduced number of gametophores in comparison with the wild type, although the genes responsible have not been identified. This defect was augmented by the exogenous addition of cytokinin or the induction of a cytokinin biosynthesis gene (Ashton et al, 1979;Abel et al, 1989;Reutter et al, 1998). In addition, the number of gametophores decreased in the BAR 77 mutant line, and the exogenous addition of auxin exacerbated the defect, indicating that auxin is also involved in the formation of…”
Section: Interaction Of Apbs With Auxin and Cytokininmentioning
confidence: 99%
“…In order to monitor mitochondria and ER simultaneously in a plant, we used fluorescently labeled organelles of the model moss Physcomitrella patens, which provides a uniquely high rate of homologous recombination in plants (Strepp et al, 1998) and is amenable to confocal microscopy studies (Abel et al, 1989;Furt et al, 2012;Vidali and Bezanilla, 2012;Müller et al, 2015). We generated a stable transgenic moss line constitutively expressing mitochondria-targeted mEOS (mtEOS; Mathur et al, 2010) and transiently transfected protoplasts of this line with an ER marker that comprises a signal peptide, mCerulean, and a C-terminal KDEL ER retention signal (spCerKDEL).…”
Section: Resultsmentioning
confidence: 99%