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Abstract
Transgene expression from the chloroplast (plastid) genome offers several attractions to plant biotechnologists, including high-level accumulation of foreign proteins, transgene stacking in operons and a lack of epigenetic interference with the stability of transgene expression. In addition, the technology provides an environmentally benign method of plant genetic engineering, because plastids and their genetic information are maternally inherited in most crops and thus are largely excluded from pollen transmission. During the past few years, researchers in both the public and private sectors ...
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Abstract
Plastids fulfill a number of essential functions, including photosynthesis, assimilation of nitrogen and sulfur, synthesis of amino acids, fatty acids, and many secondary metabolites. Pure computation-based predictions are limited in predicting plastid proteomes, and proteomic and especially subcellular proteomics studies are essential to provide an in-depth evaluation of the plastid proteome. The aim of this chapter was to highlight some of the current data, generated by plastids proteomics, in terms of functions, compartmentation, and evolution of this organelle. ...
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Abstract
Plant chloroplasts contain an intricate photosynthetic membrane system, the thylakoids, and are surrounded by two envelope membranes at which thylakoid lipids are assembled. The glycoglycerolipids mono- and digalactosyldiacylglycerol, and sulfoquinovosyldiacylglycerol as well as phosphatidylglycerol, are present in thylakoid membranes, giving them a unique composition. Fatty acids are synthesized in the chloroplast and are either directly assembled into thylakoid lipids at the envelope membranes or exported ...
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Trends Plant Sci, Vol. 9, No. 6. (2004), pp. 293-301
Abstract
The chloroplast is a compartment unique to photosynthetic eukaryotes. It and other members of the plastid family carry out a remarkable range of activities. Explorations of photosynthesis-related phenomena have stimulated biochemical, biophysical, molecular and genetic approaches to understanding the proplastid-to-chloroplast conversion and the regulation of chloroplast processes. Much of this regulation is exerted by nuclear gene products, which often participate in plastid gene expression. Concerted exploitation of genomic resources promises a deeper understanding of these regulatory factors and more effective genetic ...
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Abstract
Stromules are stroma-filled tubules that extend from the surface of plastids and allow the transfer of proteins as large as 550 kDa between interconnected plastids. The aim of the present study was to determine if plastid DNA or plastid ribosomes are able to enter stromules, potentially permitting the transfer of genetic information between plastids. Plastid DNA and ribosomes were marked with green fluorescent protein (GFP) fusions to LacI, the lac repressor, which binds to lacO-related sequences in plastid DNA, and to plastid ...
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Abstract
Kleptoplastidy is the retention of plastids obtained from ingested algal prey, which may remain temporarily functional and be used for photosynthesis by the predator. We showed that the marine dinoflagellate Dinophysis mitra has great kleptoplastid diversity. We obtained 308 plastid rbcL sequences by gene cloning from 14 D. mitra cells and 102 operational taxonomic units (OTUs). Most sequences were new in the genetic database and ...
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Abstract
The development of chloroplasts and the integration of their function within a plant cell rely on the presence of a complex biochemical machinery located within their limiting envelope membranes. To provide the most exhaustive view of the protein repertoire of chloroplast envelope membranes, we analyzed this membrane system using proteomics. To this purpose, we first developed a procedure to prepare highly purified envelope membranes from Arabidopsis chloroplasts. We then extracted envelope proteins using different methods, i.e. chloroform/methanol extraction and alkaline or ...
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posted to gfp plastid stromules
by dandaman
on 2012-07-11 09:29:26
Abstract
Two envelope membranes delimit plastids, the defining organelles of plant cells. The inner and outer envelope membranes are unique in their protein and lipid composition. Several studies have attempted to establish the proteome of these two membranes; however, differentiating between them is difficult due to their close proximity. Here, we describe a novel approach to distinguish the localization of proteins between the two membranes using ...
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Abstract
Organelles are surrounded by membranes with a distinct lipid and protein composition. While it is well established that lipids affect protein functioning and vice versa, it has been only recently suggested that elevated membrane protein concentrations may affect the shape and organization of membranes. We therefore analyzed the effects of high chloroplast envelope protein concentrations on membrane structures using an in vivo approach with protoplasts. ...
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posted to daidalos first_year plastid
by fuenfgeld
on 2012-05-22 10:04:04
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Trends in Plant Science, Vol. 6, No. 4. (2001), pp. 151-155
Abstract
The plastid nucleoid consists of plastid DNA and various, mostly uncharacterized, DNA-binding proteins. The plastid DNA undoubtedly originated from an ancestral cyanobacterial genome, but the origin of the nucleoid proteins appears complex. Initial biochemical analysis of these proteins, as well as comparative genome informatics, suggest that proteins of eukaryotic origin replaced most of the original prokaryotic proteins during the evolution of plastids in the lineage of green plants. ...
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Current Opinion in Plant Biology, Vol. 4, No. 3. (2001), pp. 210-218
Abstract
The general scheme of carotenoid biosynthesis has been known for more than three decades. However, molecular description of the pathway in plants began only in the 1990s after the genes for the carotenogenic enzymes were cloned. Recent data on the biochemistry of carotenogenesis and its regulation in vivo present the possibility of genetically manipulating this pathway in crop plants. ...
Note (first note only)
TY - JOUR
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Abstract
All plant cells contain plastids. Various reactions are located exclusively within these unique organelles, requiring the controlled exchange of a wide range of solutes, ions, and metabolites. In recent years, several proteins involved in import and/or export of these compounds have been characterized using biochemical and electrophysiological approaches, and in addition have been identified at the molecular level. Several solute channels have been identified in the outer envelope membrane. These porin-like proteins in the outer envelope membrane were formerly thought to ...
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American Journal of Botany, Vol. 91, No. 10. (2004), pp. 1481-1493
Abstract
By synthesizing data from individual gene phylogenies, large concatenated gene trees, and other kinds of molecular, morphological, and biochemical markers, we begin to see the broad outlines of a global phylogenetic tree of eukaryotes. This tree is apparently composed of five large assemblages, or ‘‘supergroups.’’ Plants and algae, or more generally eukaryotes with plastids (the photosynthetic organelle of plants and algae and their nonphotosynthetic derivatives) are scattered among four of the five supergroups. This is because plastids have had a complex ...
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Abstract
The genomes of DNA-containing cell organelles (mitochondria, chloroplasts) can be laterally transmitted between organisms, a process known as organelle capture. Organelle capture often occurs in the absence of detectable nuclear introgression, and the capture mechanism is unknown. Here, we have considered horizontal genome transfer across natural grafts as a mechanism underlying chloroplast capture in plants. By grafting sexually incompatible species, we show that complete chloroplast genomes can travel across the graft junction from one species into another. We demonstrate that, consistent ...
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by Myriam Ferro, Sabine Brugière, Daniel Salvi, et al.Daphné Seigneurin-Berny, Magali Court, Lucas Moyet, Claire Ramus, Stéphane Miras, Mourad Mellal, Sophie Le Gall, Sylvie Kieffer-Jaquinod, Christophe Bruley, Jérôme Garin, Jacques Joyard, Christophe Masselon, Norbert Rolland
Abstract
Recent advances in the proteomics field have allowed a series of high throughput experiments to be conducted on chloroplast samples, and the data are available in several public databases. However, the accurate localization of many chloroplast proteins often remains hypothetical. This is especially true for envelope proteins. We went a step further into the knowledge of the chloroplast proteome by focusing, in the same set ...
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Abstract
The introduction of plastids into different heterotrophic protists created lineages of algae that diversified explosively, proliferated in marine and freshwater environments, and radically altered the biosphere. The origins of these secondary plastids are usually inferred from the presence of additional plastid membranes. However, two examples provide unique snapshots of secondary-endosymbiosis-in-action, because they retain a vestige of the endosymbiont nucleus known as the nucleomorph. These are chlorarachniophytes and cryptomonads, which acquired their plastids from a green and red alga respectively. To allow ...
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by Ganesh Kumar K. Agrawal, Jacques Bourguignon, Norbert Rolland, et al.Geneviève Ephritikhine, Myriam Ferro, Michel Jaquinod, Konstantinos G. Alexiou, Thierry Chardot, Niranjan Chakraborty, Pascale Jolivet, John H. Doonan, Randeep Rakwal
Abstract
Organelle proteomics describes the study of proteins present in organelle at a particular instance during the whole period of their life cycle in a cell. Organelles are specialized membrane bound structures within a cell that function by interacting with cytosolic and luminal soluble proteins making the protein composition of each organelle dynamic. Depending on organism, the total number of organelles within a cell varies, indicating ...
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posted to plastid transformation
by jamerca
on 2011-03-29 08:55:54
Abstract
Summary Plastid transformation is widely used in basic research and for biotechnological applications. Initially developed in Chlamydomonas and tobacco, it is now feasible in a broad range of species. Selection of transgenic lines where all copies of the polyploid plastid genome are transformed requires efficient markers. A number of traits have been used for selection such as photoautotrophy, resistance to antibiotics and tolerance to herbicides or to other metabolic inhibitors. Restoration of photosynthesis is an effective primary selection method in Chlamydomonas ...
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posted to plastid review
by icq242500260
on 2011-02-27 23:13:13
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posted to chloroplast ontogeny plastid
by icq242500260
on 2011-02-27 01:22:00
Abstract
Imaging of chlorophyll autofluorescence by confocal microscopy in intact whole petals of Arabidopsis thaliana has been used to analyze chloroplast development and redifferentiation during petal development. Young petals dissected from unopened buds contained green chloroplasts throughout their structure, but as the upper part of the petal lamina developed and expanded, plastids lost their chlorophyll and redifferentiated into leukoplasts, resulting in a white petal blade. Normal green chloroplasts remained in the stalk of the mature petal. In epidermal cells the chloroplasts were ...
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posted to plastid
by icq242500260
on 2011-02-24 00:53:01
Abstract
Plastids are vital organelles, fulfilling important metabolic functions that greatly influence plant growth and productivity. In order to both regulate and harness the metabolic output of plastids, it is vital that the process of plastid division is carefully controlled. This is essential, not only to ensure persistence in dividing plant cells and that optimal numbers of plastids are obtained in specialized cell types, but also to allow the cell to act in response to developmental signals and environmental changes. How this ...
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posted to plastid
by icq242500260
on 2011-02-24 00:51:19
Abstract
Extrapolation from the mechanism of bacterial cell division provides valuable clues as to how the chloroplast division process is achieved in plant cells. However, it is becoming increasingly clear that the highly regulated mechanism of plastid division within the host cell has led to the evolution of features unique to the plastid division process. ...
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Abstract
SummaryThe Plantae comprising red, green (including land plants), and glaucophyte algae are postulated to have a single common ancestor that is the founding lineage of photosynthetic eukaryotes [[1] and [2]]. However, recent multiprotein phylogenies provide little [[3] and [4]] or no [[5] and [6]] support for this hypothesis. This may reflect limited complete genome data available for red algae, currently only the highly reduced genome of Cyanidioschyzon merolae [7], a reticulate gene ancestry [5], or variable gene divergence rates that ...
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posted to plastid
by icq242500260
on 2011-02-19 02:32:47
Abstract
Plastid genes are expressed at high levels in photosynthetically active chloroplasts but are generally believed to be drastically downregulated in nongreen plastids. The genome-wide changes in the expression patterns of plastid genes during the development of nongreen plastid types as well as the contributions of transcriptional versus translational regulation are largely unknown. We report here a systematic transcriptomics and translatomics analysis of the tomato (Solanum ...
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Gene, Vol. 280 (2001), pp. 19-26
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posted to plastid
by icq242500260
on 2011-01-14 23:34:52
Abstract
Plastids are crucial to plant functionality and develop from proplastids in meristem cells to generate different plastid forms in different types of plant cells. In addition to the photosynthesis of leaf mesophyll cell chloroplasts, plastids contribute to storage and pigmentation capacities in many different specialised cells as well as contributing essential metabolic pathways within the cell in general. Plastids also have the capacity to interconvert between types according to environmental and molecular signals. Progress in understanding the cell biology and morphological ...
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posted to plastid
by icq242500260
on 2011-01-14 23:33:44
Abstract
Plastids are semiautonomous organelles found, in one form or another, in practically all plant and algal cells, several taxa of marine mollusks and at least one phylum of parasitic protists. The members of the plastid family play pivotal roles in photosynthesis, amino acid and lipid synthesis, starch and oil storage, fruit and flower coloration, gravity sensing, stomatal functioning, and environmental perception. Plastids arose via an endosym biotic event in which a protoeukaryotic cell engulfed and retained a photosynthetic bacterium. This polyphyletic ...
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by Yamato Yoshida, Haruko Kuroiwa, Osami Misumi, et al.Masaki Yoshida, Mio Ohnuma, Takayuki Fujiwara, Fumi Yagisawa, Shunsuke Hirooka, Yuuta Imoto, Kazunobu Matsushita, Shigeyuki Kawano, Tsuneyoshi Kuroiwa
posted to ftsz plastid plastid_division
by dandaman
on 2010-12-16 15:50:29
Abstract
In chloroplast division, the plastid-dividing (PD) ring is a main structure of the PD machinery and is a universal structure in the plant kingdom. However, the components and formation of the PD ring have been enigmatic. By proteomic analysis of PD machineries isolated from Cyanidioschyzon merolae, we identified the glycosyltransferase protein plastid-dividing ring 1 (PDR1), which constructs the PD ring and is widely conserved from red alga to land plants. Electron microscopy showed that the PDR1 protein forms a ring with ...
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Abstract
BACKGROUND:The cultivated olive (Olea europaea L.) is the most agriculturally important species of the Oleaceae family. Although many studies have been performed on plastid polymorphisms to evaluate taxonomy, phylogeny and phylogeography of Olea subspecies, only few polymorphic regions discriminating among the agronomically and economically important olive cultivars have been identified. The objective of this study was to sequence the entire plastome of olive and analyze many potential polymorphic regions to develop new inter-cultivar genetic markers.RESULTS:The complete plastid genome of the olive ...
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posted to alga dinoflagellate plastid
by bgranger
on 2010-06-11 15:18:25
Abstract
The discovery of a nonphotosynthetic plastid in malaria and other apicomplexan parasites has sparked a contentious debate about its evolutionary origin. Molecular data have led to conflicting conclusions supporting either its green algal origin or red algal origin, perhaps in common with the plastid of related dinoflagellates. This distinction is critical to our understanding of apicomplexan evolution and the evolutionary history of endosymbiosis and photosynthesis; however, the two plastids are nearly impossible to compare due to their nonoverlapping information content. Here ...
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Proceedings of the National Academy of Sciences of the United States of America, Vol. 104, No. 49. (4 December 2007), pp. 19363-8, doi:10.1073/pnas.0708072104
Abstract
Although great progress has been made in clarifying deep-level angiosperm relationships, several early nodes in the angiosperm branch of the Tree of Life have proved difficult to resolve. Perhaps the last great question remaining in basal angiosperm phylogeny involves the branching order among the five major clades of mesangiosperms (Ceratophyllum, Chloranthaceae, eudicots, magnoliids, and monocots). Previous analyses have found no consistent support for relationships among these clades. In an effort to resolve these relationships, we performed phylogenetic analyses of 61 plastid ...
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Abstract
Plastids including chloroplasts arose from a cyanobacterial endosymbiont and have retained their own genome, but the size has been reduced to less than one-tenth of the original bacterial genome. Over time, genes essential to plastid function have been transferred from the ancestral plastid genome to the nucleus, and the gene products are now targeted into the plastid from the host cytosol. However, phylogenetic analyses have suggested that the functions of certain original proteins encoded by the endosymbiont genome have been replaced ...
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Abstract
The green algae belonging to the Chlorophyta--the lineage sister to that comprising the land plants and their charophycean green algal relatives (Streptophyta)--have been subdivided into four classes (Prasinophyceae, Ulvophyceae, Trebouxiophyceae, and Chlorophyceae). Yet the Pedinomonadales, an assemblage consisting of tiny, naked uniflagellates with a second basal body, has no clear affiliation with these classes and the branching order of the crown chlorophytes remains unknown. To gain an insight into the phylogenetic position of the Pedinomonadales and the relationships among the recognized ...
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PLANT CELL AND ENVIRONMENT, Vol. {29}, No. {3}. (MAR {2006})
Abstract
Carotenoids are plant pigments that function as antioxidants, hormone precursors, colourants and essential components of the photosynthetic apparatus. Carotenoids accumulate in nearly all types of plastids, not just the chloroplast, and are thus found in most plant organs and tissues, albeit at trace levels in some tissues. In this review we summarise the current knowledge of the carotenoid content of non-green plastids and discuss what is known about the regulation of their biosynthesis in roots, fruits, flowers, tubers and seeds. The ...
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In Molecular Genetics and Genomics, Vol. 275, No. 4. (2006), 367-373
Abstract
The tobacco cultivar Nicotiana tabacum is a natural amphidiploid that is thought to be derived from ancestors of Nicotiana sylvestris and Nicotiana tomentosiformis. To compare these chloroplast genomes, DNA was prepared from isolated chloroplasts from green leaves of N. sylvestris and N. tomentosiformis, and subjected to whole-genome shotgun sequencing. The N. sylvestris chloroplast genome comprises of 155,941 bp and shows identical gene organization with that of N. tabacum, except one ORF. Detailed comparison revealed only seven different sites between N. tabacum ...
Note (first note only)
Times Cited: 2
Cited Reference Count: 26
Cited References:
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FULNECEK J, 2002, HEREDITY 1, V88, P19
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HUPFER H, 2000, MOL GEN GENET, V263, P581
KUNG SD, 1982, THEOR APPL GENET, V61, P73
MARTIN W, 1998, NATURE, V393, P162
MAUL JE, 2002, PLANT CELL, V14, P2659
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OLMSTEAD R, 1991, SOLANACEAE 3 TAXONOM, P301
PALMER JD, 1991, MOL BIOL PLASTIDS,
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In Plant Systematics and Evolution, Vol. 226, No. 1-2. (2001), 85-107
Abstract
The phylogeny of the genus Gunnera is investigated for the first time. Twelve species representing the six currently recognised subgenera are analysed. Two chloroplast DNA regions, the rbcL gene and the rps16 intron, together provide 46 informative characters out of 2335. A combined analysis of both genes gives four most parsimonious trees, firmly establishing the east South American G. herteri as sister group to the rest of the genus. The African G. perpensa is sister group to two well-supported clades, one ...
Note (first note only)
Times Cited: 17
Cited Reference Count: 52
Cited References:
*LINN, 1967, MANTISSA PLANTARUM S
ANDERBERG AA, 1998, PLANT SYST EVOL, V211, P93
ARWIDSSON T, 1938, REV SUDAMER BOT, V5, P157
BADER FWJ, 1961, BOT JB, V80, P281
BREMER K, 1994, CLADISTICS, V10, P295
BRUNDIN L, 1966, KUNGL SVENSKA VETENS, V11, P1
CHASE MW, 1993, ANN MISSOURI BOT GAR, V80, P523
CRONQUIST A, 1981, INTEGRATED SYSTEM CL
DAHLGREN R, 1975, BOT NOTISER, V128, P182
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ENDRESS PK, 1989, EVOLUTION SYSTEMATIC, V1, P193
ERIKSSON T, 1995, AUTODECAY 3 0
FELSENSTEIN J,
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In Molecular Phylogenetics and Evolution, Vol. 38, No. 2. (2006), 398-415
Abstract
Sequence data from the low-copy nuclear genes encoding phosphoribulokinase (PRK) and the second largest subunit of RNA polymerase II (RPB2) are used to generate the first phylogenetic analysis of Chamaedorea (Arecaceae: Arecoideae: Chamaedoreeae), the largest neotropical genus of palms. The prevailing current taxonomy of Chamaedorea recognizes approximately 100 species in eight subgenera, all delimited using floral characters, which provide a useful starting point to explore species-level systematics. Sequence data from 63 species, including representatives of all eight subgenera, were analyzed using ...
Note (first note only)
Times Cited: 2
Cited Reference Count: 52
Cited References:
ALTSCHUL SF, 1997, NUCLEIC ACIDS RES, V25, P3389
ASMUSSEN CB, 1999, MEM NEW YORK BOTAN G, V83, P121
ASMUSSEN CB, 2000, CSIRO SYDNEY, V1, P525
ASMUSSEN CB, 2001, AM J BOT, V88, P1103
BAKER WJ, 1999, PLANT SYST EVOL, V219, P111
BAKER WJ, 2000, MOL PHYLOGENET EVOL, V14, P195
BAKER WJ, 2000, MOL PHYLOGENET EVOL, V14, P218
BARROW S, 1999, MEM NEW YORK BOTAN G, V83, P215
BRIDGEWATER S, UNPUB EC BOT
BRIDGEWATER SGM, UNPUB EC BOT
DOUADY CJ, 2003, MOL BIOL EVOL, V20, P248
DOYLE
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In Plant Journal, Vol. 40, No. 2. (2004), 314-321
Abstract
Three distinct arginine tRNA genes, trnR-CCG, trnR-ACG, and trnR-UCU, are present in the plastid genome of bryophytes, whereas only the latter two trnR genes are present in the major vascular plants, except for black pine. trnR-CCG is located between rbcL and accD in the moss Physcomitrella patens and it was previously believed to be functional in plastids. However, no trnR-CCG transcript has been detected by Northern hybridization, and the codon usage of CGG is quite low in plastid protein-coding sequences. This ...
Note (first note only)
Times Cited: 10
Cited Reference Count: 35
Cited References:
ASHTON NW, 1977, MOL GEN GENET, V154, P87
BEZANILLA M, 2003, PLANT PHYSIOL, V133, P470
BOYNTON JE, 1988, SCIENCE, V240, P1534
COVE DJ, 1993, PLANT CELL, V5, P1483
CRICK FHC, 1966, J MOL BIOL, V19, P548
GOLDS T, 1993, BIO-TECHNOL, V11, P95
HOHE A, 2002, PLANT BIOLOGY, V4, P595
KASTEN B, 1991, NUCLEIC ACIDS RES, V19, P5074
KASTEN B, 1992, CURR GENET, V22, P327
KHAN MS, 1999, NAT BIOTECHNOL, V17, P910
KOHCHI T, 1988, J MOL BIOL, V203, P353
KUGITA M, 2003, NUCLEIC ACIDS RES, V31,
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In Nucleic Acids Research, Vol. 31, No. 18. (2003), 5324-5331
Abstract
The complete chloroplast DNA sequence ( 122 890 bp) of the moss Physcomitrella patens has been determined. The genome contains 83 protein, 31 tRNA and four rRNA genes, and a pseudogene. Four protein genes ( rpoA, cysA, cysT and ccsA) found in the liverwort Marchantia polymorpha and the hornwort Anthoceros formosae are absent from P. patens. The overall structure of P. patens chloroplast DNA (cpDNA) differs substantially from that of liverwort and hornwort. Compared with its close relatives, a 71 kb ...
Note (first note only)
Times Cited: 27
Cited Reference Count: 50
Cited References:
*AR GEN IN, 2000, NATURE, V408, P796
CALIE PJ, 1987, MOL GEN GENET, V208, P335
EMANUELSSON O, 2000, J MOL BIOL, V300, P1005
GOFF SA, 2002, SCIENCE, V296, P92
GOLDSCHMIDTCLERMONT M, 1991, CELL, V65, P135
HALLICK RB, 1993, NUCLEIC ACIDS RES, V21, P3537
HARA K, 2001, BBA-GENE STRUCT EXPR, V1517, P302
HARA K, 2001, FEBS LETT, V499, P87
HESS WR, 1999, INT REV CYTOL, V190, P1
HIRATSUKA J, 1989, MOL GEN GENET, V217, P185
IGARASHI K, 1991, CELL, V65, P1015
IGARASHI K, 1991, J MOL BIOL,
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In DNA Research, Vol. 12, No. 3. (2005), 215-220
Abstract
The complete nucleotide sequence of the chloroplast genome of the hardwood species Eucalyptus globulus is presented and compared with chloroplast genomes of tree and non-tree angiosperms and two softwood tree species. The 160 286 bp genome is similar in gene order to that of Nicotiana, with an inverted repeat (IR) (26 393 bp) separated by a large single copy (LSC) region of 89 012 bp and a small single copy region of 18 488 bp. There are 128 genes (112 individual ...
Note (first note only)
Times Cited: 7
Cited Reference Count: 24
Cited References:
BENDICH AJ, 2004, PLANT CELL, V16, P1661
BOUDREAU E, 1997, EMBO J, V16, P6095
DOYLE JJ, 1990, FOCUS, V12, P13
DRESCHER A, 2000, PLANT J, V22, P97
ELDRIDGE KG, 1993, EUCALYPT DOMESTICATI
EWING B, 1998, GENOME RES, V8, P186
GOREMYKIN VV, 2003, MOL BIOL EVOL, V20, P1499
HUPFER H, 2000, MOL GEN GENET, V263, P581
KUDLA J, 1992, EMBO J, V11, P1099
KUGITA M, 2003, NUCLEIC ACIDS RES, V31, P716
LIU XQ, 1993, PLANT MOL BIOL, V23, P297
MILLEN RS, 2001, PLANT CELL, V13, P645
OLDENBURG DJ,
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In American Journal of Botany, Vol. 92, No. 9. (2005), 1575-1585
Abstract
The evolution of holoparasitism decreases the adaptive value of genes maintaining the photosynthetic apparatus. These may become pseudogenes through insertion or deletion events resulting in frameshift mutations, or by the evolution of premature stop codons. The holoparasitic sister genera Harveya and Hyobanche have undergone alternate pathways of evolution and expression at the plastid locus rbcL. An open reading frame in all but a single species of Harveya is maintained by purifying selection and is expressed. However, the function of Rubisco in ...
Note (first note only)
Times Cited: 0
Cited Reference Count: 65
Cited References:
*SPSS INC, 1999, SPSS WIND
BOMMER D, 1993, CURR GENET, V24, P171
BRICAUD CH, 1986, J PLANT PHYSIOL, V125, P367
BUNGARD RA, 2004, BIOESSAYS, V26, P235
COLWELL A, 1994, THESIS WASHINGTON U
DANON A, 1997, PLANT PHYSIOL, V115, P1293
DELAHARPE AC, 1980, Z PFLANZENPHYSIOL, V100, P85
DELAHARPE AC, 1981, Z PFLANZENPHYSIOL, V103, P265
DELAVAULT P, 1995, PLANT MOL BIOL, V29, P1071
DELAVAULT PM, 1996, PHYSIOL PLANTARUM, V96, P674
DEPAMPHILIS CW, 1990, NATURE, V348, P337
DORR I, 1995, BOT ACTA, V108, P47
DOYLE JJ, 1987, PHYTOCHEMISTRY B, V19,
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In Plant Systematics and Evolution, Vol. 247, No. 3-4. (2004), 203-213
Abstract
The orchid subfamily Apostasioideae consists of two genera, Apostasia and Neuwiedia. To study the position of Apostasioideae within Orchidaceae and their intra- and intergeneric relationships, a molecular phylogenetic analysis has been conducted on the nuclear ITS region and the two plastid DNA regions trnL-F intron and matK. The two genera traditionally ascribed to Apostasioideae are each monophyletic. In Apostasia, A. nuda, with two stamens and no staminode, is sister to a clade comprising three species characterised by two stamens and one ...
Note (first note only)
Times Cited: 9
Cited Reference Count: 43
Cited References:
BALDWIN BG, 1992, MOL PHYLOGENET EVOL, V1, P3
BURNSBALOGH P, 1986, SMITHSONIAN CONTRIBU, V61, P1
CAMERON KM, 1999, AM J BOT, V86, P208
CAMERON KM, 2000, MONOCOTS SYSTEMATICS, P457
CAMERON KM, 2001, AM J BOT, V88, P1847
CAMERON KM, 2003, MONOCOTS, V3
CHASE MW, 2000, MONOCOTS SYSTEMATICS, P3
CHASE MW, 2003, ORCHID CONSERVATION, P69
CONTI E, 1999, MOL PHYLOGENET EVOL, V13, P536
COX AV, 1997, PLANT SYST EVOL, V208, P197
DEVOGEL EF, 1969, BLUMEA, V17, P312
DOYLE JJ, 1987, PHYTOCHEMISTRY B, V19, P11
EICHENBERGER K, 2000, BOT
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In Gene, Vol. 297, No. 1-2. (2002), 85-92
Abstract
Orobanche species characterization using plastid sequences as molecular markers revealed that O. cumana contains at least two distinct rbcL sequences: one similar in size to the truncated rbcL pseudogene from O. cernua, a closely related species, and another with a size comparable to that of rbcL plastid genes from autotrophic plants. In this work, the nucleotide sequences of these two copies are reported and analysed. The organization of the O. cumana plastid genome was investigated using a long-distance PCR strategy in ...
Note (first note only)
Times Cited: 2
Cited Reference Count: 21
Cited References:
AYLIFFE MA, 1992, THEOR APPL GENET, V85, P229
AYLIFFE MA, 1998, MOL BIOL EVOL, V15, P738
BENHARRAT H, 2000, PLANT BIOLOGY, V2, P34
BLANCHARD JL, 1995, J MOL EVOL, V41, P397
CHEUNG WY, 1989, THEOR APPL GENET, V77, P625
CORMACK RS, 1997, GENE, V194, P273
DELAVAULT PM, 1996, PHYSIOL PLANTARUM, V96, P674
DEPAMPHILIS CW, 1990, NATURE, V348, P337
LUSSON NA, 1998, CURR GENET, V34, P212
MARTIN W, 1998, PLANT PHYSIOL, V118, P9
NAKAZONO M, 1993, MOL GEN GENET, V236, P341
PICHERSKY E, 1991, MOL GEN GENET,
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In Plant Biology, Vol. 2, No. 1. (2000), 34-39
Abstract
Among members of the Orobanchaceae, parasitism has led to a drastic reduction in the morphological characters useful in identification. This is especially the case of species belonging to the subsection Minores (section Orobanche), which is a real tangle for agronomists and botanists. In this study, more than 120 specimens collected in the west of France were studied for their morphological characters and molecular markers. Their rbcL plastid gene was analyzed by RFLP and nucleotide sequencing. Because of several substitutions, insertions and ...
Note (first note only)
Times Cited: 4
Cited Reference Count: 33
Cited References:
ABUSBAIH H, 1994, BIOL MANAGEMENT OROB, P112
ANDARY C, 1994, BIOL MANAGEMENT OROB, P121
BONNIER G, 1934, FLORE COMPLETE ILLUS
CHATER AO, 1972, FLORA EUROPAEA, V3, P285
COSTE H, 1906, FLORE DESCRIPTIVE IL
DELAVAULT P, 1995, PLANT MOL BIOL, V29, P1071
DEPAMPHILIS CW, 1990, NATURE, V348, P337
DEPAMPHILIS CW, 1997, P NATL ACAD SCI USA, V94, P7367
FOURNIER G, 1961, QUATRE FLORES FRANCE
GEORGUIEVA I, 1994, BIOL MANAGEMENT OROB, P127
HABERHAUSEN G, 1994, PLANT MOL BIOL, V24, P217
HARDTKE CS, 1996, PLANT MOL BIOL, V32, P915
JOEL
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In Acta Physiologiae Plantarum, Vol. 27, No. 4B. (2005), 651-664
Abstract
Microspore embryogenesis is a method of great importance for plant production in many species. Its practical use in monocotyledonous plants, however, is limited due to the occurrence of albino plants. Molecular examinations of such albino plants showed an aberrant form of plastids and, frequently, deletions in their plastid DNA. Moreover, in Our preceding work we found typical deficiencies in plastid transcription and translation. Nevertheless, there are also indications for an involvement of the nuclear genome in albino plant formation. To address ...
Note (first note only)
Times Cited: 0
Cited Reference Count: 63
Cited References:
ABDALLAH F, 2000, TRENDS PLANT SCI, V5, P141
AGACHE S, 1989, THEOR APPL GENET, V77, P7
AHLERT D, 2003, P NATL ACAD SCI USA, V100, P15730
ALLISON LA, 1996, EMBO J, V15, P2802
ALTSCHUL SF, 1990, J MOL BIOL, V215, P403
ANKELE E, 1998, THESIS U AGR VIENNA
ANKELE E, 2003, THESIS U VIENNA
AVNI A, 1989, EMBO J, V8, P1915
CAREDDA S, 2000, SEX PLANT REPROD, V13, P95
CAREDDA S, 2004, PLANT CELL TISS ORG, V76, P35
CLEMENT C, 2005, BIOTECHNOL AGRIC FOR, V56,
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Abstract
Plastid genome content and arrangement are highly conserved across most land plants and their closest relatives, streptophyte algae, with nearly all plastid introns having invaded the genome in their common ancestor at least 450 million years ago. One such intron, within the transfer RNA trnK-UUU, contains a large open reading frame that encodes a presumed intron maturase, matK. This gene is missing from the plastid genomes of two species in the parasitic plant genus Cuscuta but is found in all other ...
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Proceedings of the National Academy of Sciences of the United States of America, Vol. 89, No. 22. (15 November 1992), pp. 10648-10652
posted to monotropa plastid
by jamesgwallis
on 2009-08-11 23:29:47
Abstract
Complete nucleotide sequencing shows that the plastid genome of Epifagus virginiana, a nonphotosynthetic parasitic flowering plant, lacks all genes for photosynthesis and chlororespiration found in chloroplast genomes of green plants. The 70,028-base-pair genome contains only 42 genes, at least 38 of which specify components of the gene-expression apparatus of the plastid. Moreover, all chloroplast-encoded RNA polymerase genes and many tRNA and ribosomal protein genes have been lost. Since the genome is functional, nuclear gene products must compensate for some gene losses ...
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Proceedings of the National Academy of Sciences of the United States of America, Vol. 105, No. 47. (25 November 2008), pp. 18424-18429, doi:10.1073/pnas.0806759105
posted to genome monotropa plastid
by jamesgwallis
on 2009-08-11 23:27:41
Abstract
Angiosperm plastid genomes are generally conserved in gene content and order with rates of nucleotide substitutions for protein-coding genes lower than for nuclear protein-coding genes. A few groups have experienced genomic change, and extreme changes in gene content and order are found within the flowering plant family Geraniaceae. The complete plastid genome sequence of Pelargonium X hortorum (Geraniaceae) reveals the largest and most rearranged plastid genome identified to date. Highly elevated rates of sequence evolution in Geraniaceae mitochondrial genomes have been ...
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