- Open Access
Interorganellar crosstalk: new perspectives on signaling from the chloroplast to the nucleus
© BioMed Central Ltd 2001
- Published: 30 July 2001
Chlorophyll precursors, photosynthetic electron transport, and sugars have all been shown to be involved in signaling from the chloroplast to the nucleus, suggesting the presence of multiple signaling pathways of coordination between these two cellular compartments.
- Photosynthetic Electron Transport
- Chlorophyll Biosynthesis
- Photosynthetic Gene
- Functional Chloroplast
The endosymbiotic theory of chloroplast evolution proposes that a photosynthetic prokaryote was engulfed by a eukaryotic host to produce the eukaryotic plant cell. The ensuing endosymbiosis resulted in gene transfer from the chloroplast genome to the nuclear genome, and thus the chloroplast contains both nucleus-encoded and chloroplast-encoded components. The development of a fully functional chloroplast therefore depends on the coordinate expression of nuclear and chloroplast genes in response to both developmental and environmental signals. Chloroplast function requires the import of both nucleus-encoded photosynthetic proteins and cytoplasmic factors that regulate the expression of chloroplast genes. The plastid also plays a role in nuclear gene expression, with signals that originate in the chloroplast acting to regulate transcription of nucleus-encoded photosynthetic genes. In the last ten years, many studies have revealed the nature of nucleus-derived molecules that affect chloroplast gene expression at all levels (reviewed in [1,2,3]). Although it has been known for many years that the expression of a subset of nuclear genes, whose products are involved in photosynthesis, depends on the presence in the cell of functional plastids , little progress has been made in elucidating the signaling molecules or mechanisms involved in this retrograde signaling. Several recent discoveries have made inroads into this complex mechanism [5,6,7,8] and have begun to shed light on the black box of signaling from the chloroplast to the nucleus.
It has long been suspected that chlorophyll precursors play a role in signaling to the nucleus. Indirect evidence came from reports of the repression of nuclear photosynthetic genes in Chlamydomonas reinhardtii by the addition of a specific inhibitor of chlorophyll biosynthesis that results in chlorophyll-precursor accumulation [9,10]. The same chlorophyll precursors have also been reported to act as inducers of nucleus-encoded cytosolic and chloroplast-localized heat-shock proteins [11,12].
Two recent papers, by Mochizuki et al.  and Møller et al. , have identified proteins involved in chlorophyll biosynthesis as regulators of light-stimulated expression of nucleus-encoded photosynthetic genes such as those encoding the light-harvesting chlorophyll a/b binding protein (Lhcb), Rubisco small subunit (RbcS), chalcone synthase (Chs) and ferredoxin-NADP reductase (Fnr).
Møller et al. isolated Arabidopsis long after far red (laf) mutants displaying reduced hypocotyl-growth inhibition in response to far-red light. These mutants also have an inability to become green following treatment with far-red light, and they have reduced expression of the light-regulated genes Lhcb, Chs, and Fnr in far-red light. LAF6 was cloned and shown to encode a novel plant member of the small soluble ATP-binding-cassette transporter family (atABC1); members of this family are usually involved in the import of catabolites across membranes. AtABC1 has a functional amino-terminal chloroplast-transit peptide and localizes to the periphery of chloroplasts, consistent with having a position at the inner envelope. The pale-green phenotype of laf6 seedlings suggested a deficiency in chlorophyll biosynthesis. Subsequent analysis confirmed that laf6 mutants accumulate twice as much protoporphyrin IX (proto IX; see Figure 1) and 40% less chlorophyll than wild-type seedlings.
The expression of nucleus-encoded photosynthetic genes, such as Lhcb, has been shown to be repressed in the presence of high levels of sugar (reviewed in ). It has also been proposed that photosynthetic electron transport is required to activate Lhcb transcription . Oswald et al.  investigated whether these two effects operate through a common signaling pathway. They showed that photosynthetic electron transport is essential for the generation of a chloroplast signal that activates transcription of Lhcb and RbcS. This transcriptional activation did not depend on sugar status, implying that it is an independent event. Sucrose feeding repressed the transcription of Lhcb and RbcS, however, suggesting that the two pathways may interact in controlling the expression of these nuclear genes.
In studies of a mutant of the maize Sucrose export defective (Sxd1) gene, Provencher et al.  reported accumulation of sugars in photosynthetic bundle sheath cells as a result of a defect in sucrose export to the vascular parenchyma cells. The sxd1 mutant did not show repression of the nucleus-encoded photosynthetic genes Lhcb and RbcS, despite accumulation of high sugar levels. This result implies that SXD1 has a role in repression of Lhcb and RbcS in response to high sugar levels. On the basis of this observation and the localization of Sxd1 to the chloroplast, the authors proposed that SXD1 might play a role in the sugar-sensing mechanism involved in chloroplast-to-nucleus signaling.
Undoubtedly, there is still much to be discovered in this complex field. It will become increasingly difficult to study individual pathways in isolation, as one can envisage an elaborate network of crosstalk between the pathways. As these recent papers have shown, however, the search for retrograde signaling components that pass from the plastid back to the nucleus is gathering momentum.
Work in our laboratory is supported by funds from the US Department of Energy (93ER70116) and the National Institutes of Health (GM54659) to S.P.M.; E.C.B. and A.S. are supported by Skaggs post-doctoral fellowships.
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