2009
DOI: 10.1074/jbc.a402817200
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Tic32, an essential component in chloroplast biogenesis.

Abstract: On page 8628, an error has been detected in Fig. 3B (lower left panel, HCT116ϩJKA97). The corrected Fig. 3B On page 34760, we described the characterization of heterozygous T-DNA insertion lines (Fig. 4, B-D). Unfortunately, we have found that some of the presented results are invalid. To screen seedlings for heterozygous plants to be used for complementation, we ordered new primers because the old ones were no longer available. With these new primers, we found homozygous plants in both lines. The reason fo… Show more

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Cited by 21 publications
(24 citation statements)
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“…For example the schlepperless ( slp ) and tic32 mutants lack a chaperonin‐60a protein required for normal thylakoid development and a component of the plastid envelope protein translocation apparatus, respectively, but in both cases the embryo undergoes morphogenesis as far as heart stage before seed abortion occurs (Apuya et al. , 2001; Hörmann et al. , 2004).…”
Section: Discussionmentioning
confidence: 99%
See 1 more Smart Citation
“…For example the schlepperless ( slp ) and tic32 mutants lack a chaperonin‐60a protein required for normal thylakoid development and a component of the plastid envelope protein translocation apparatus, respectively, but in both cases the embryo undergoes morphogenesis as far as heart stage before seed abortion occurs (Apuya et al. , 2001; Hörmann et al. , 2004).…”
Section: Discussionmentioning
confidence: 99%
“…, 2004). For example, developmental arrest occurs in mutants that lack components of the plastid protein import machinery (Hörmann et al. , 2004; Hust and Gutensohn, 2006), and in numerous mutants defective in proteins putatively involved in chloroplast protein folding, protein synthesis and membrane synthesis and assembly (e.g.…”
Section: Introductionmentioning
confidence: 99%
“…3), suggesting roles in the regulation of import in response to endogenous redox status (Bédard & Jarvis, 2005). Whereas Tic62 and Tic32 each possess NAD(P)H binding sites, the Tic55 protein has a Rieske iron‐sulphur centre and a mononuclear iron‐binding site (Caliebe et al ., 1997; Küchler et al ., 2002; Hörmann et al ., 2004; Stengel et al ., 2008). The binding of NAD(P)H to these components might convey redox information to the translocation machinery.…”
Section: Later Stages Of the Toc/tic Pathwaymentioning
confidence: 99%
“…Some cyanobacterial proteins contain cofactor-binding motifs similar to those found in Tic62, Tic55 and Tic32. Tic55 contains a Rieske iron-sulphur centre and a mononuclear iron-binding site [11], and Tic62 and Tic32 each have a NAD(P)-binding motif [12,13]. No prokaryotic counterparts have been detected by direct sequence comparison for the other subunits that compose the translocons, which may indicate that they have evolved from the proteome of the ancestral host to fulfil specific functions demanded after the development of plastids and to ensure the specificity of the transport process in the outer/inner envelope membranes of chloroplasts.…”
Section: Introductionmentioning
confidence: 99%