2009
DOI: 10.1073/pnas.0902145106
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A search for factors influencing etioplast–chloroplast transition

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Cited by 16 publications
(17 citation statements)
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“…Most striking is the very rapid development of thylakoid membranes, increase in chlorophyll content and construction of the photosynthetic apparatus that requires both a massive import of nuclear encoded plastid proteins and high expression of plastid-encoded genes (Lonosky et al, 2004; von Zychlinski et al, 2005; Philippar et al, 2007; Pudelski et al, 2009; Majeran et al, 2010; Ploscher et al, 2011). Etioplasts display just a basic transcriptional activity and accumulate photosynthesis transcripts only to very low levels.…”
Section: Introductionmentioning
confidence: 99%
“…Most striking is the very rapid development of thylakoid membranes, increase in chlorophyll content and construction of the photosynthetic apparatus that requires both a massive import of nuclear encoded plastid proteins and high expression of plastid-encoded genes (Lonosky et al, 2004; von Zychlinski et al, 2005; Philippar et al, 2007; Pudelski et al, 2009; Majeran et al, 2010; Ploscher et al, 2011). Etioplasts display just a basic transcriptional activity and accumulate photosynthesis transcripts only to very low levels.…”
Section: Introductionmentioning
confidence: 99%
“…Unlike seedlings that undergo germination in the light, which immediately undergo photomorphogenesis, seedlings that germinate under soil follow an adaptive growth program known as skotomorphogenesis or etiolation (4)(5)(6). When seedlings finally emerge from soil, light terminates the etiolation program and activates the conversion of etioplasts to chloroplasts, which, in turn, enable the plants to gain photoautotrophic ability (7,8). This transition from darkness to light is a point of particular vulnerability in the life cycle of a higher land plants, however, due to the fact that light energy absorbed by protochlorophyllide (Pchlide) (a precursor of chlorophyll) is extremely phototoxic and can potentially cause seedling death by light-induced photooxidative damage (6,(9)(10)(11).…”
mentioning
confidence: 99%
“…Of the 16 members in the Arabidopsis (Arabidopsis thaliana) PRAT family, 10 are located in the mitochondria, with eight genes encoding for inner membrane protein transporters, specifically the Translocase of the Inner Membrane17 (Tim17), Tim23, and Tim22 . In chloroplasts, three PRAT proteins, HP20, HP30-1, and HP30-2, have been proposed to be involved in the import of proteins that do not contain a cleavable transit peptide (Rossig et al, 2013), while the outer envelope PRAT proteins OEP16.1 and OEP16.2 have been shown to be involved in amino acid transport Pudelski et al, 2009Pudelski et al, , 2010Pudelski et al, , 2012. In plants, in comparison with yeast and mammalian systems, the PRAT family appears to have undergone neofunctionalization in that, while all members are predicted to contain four transmembrane regions and a conserved/degenerate PRAT domain, additional domains also have been acquired .…”
mentioning
confidence: 99%