Chromatic Regulation in Chlamydomonas reinhardtii: Time Course of Photosystem Stoichiometry Adjustment Following a Shift in Growth Light Quality

In Chlamydomonas reinhardtii, expression of the cabII-1 gene increases dramatically in response to light (cabII-1 encodes one of the light-harvesting chlorophyll a/b-binding proteins of photosystem II). We have used a region upstream of the cabII-1 gene in translational fusions to the bacterial uidA gene (encodes beta-glucuronidase) and transcriptional fusions to the Chlamydomonas nitrate reductase gene (nit1). Chlamydomonas transformants carrying intact copies of the chimeric uidA gene do not express beta-glucuronidase at the level of enzyme activity or mRNA accumulation. Methylation in the cabII-1 promoter region of the introduced gene is extensive in these strains, suggesting that newly introduced foreign genes may be recognized and silenced by a cellular mechanism that is correlated with increased methylation. Transformants that express the chimeric cabII-1/nit1 gene have been recovered. In contrast to the endogenous nit1 gene, the chimeric cabII-1/nit1 gene is expressed in ammonium-containing medium. Moreover, nit1 mRNA accumulation is dramatically stimulated by light, with a time course that is indistinguishable from that of the endogenous cabII-1 gene. The cabII-1/nit1 gene has been used to select transformants in a nit1- nit2- Chlamydomonas strain (CC400G) and should be useful for transformation of the large number of mutants in the Ebersold-Levine lineage, which carry the same mutations.

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Gametic differentiation in Chlamydomonas reinhardtii. I. Production of gametes and their fine structure.

The Journal of Cell Biology ◽

10.1083/jcb.67.3.587 ◽

1975 ◽

Vol 67 (3) ◽

pp. 587-605 ◽

Cited By ~ 102

Author(s):

N C Martin ◽

U W Goodenough

Keyword(s):

Fine Structure ◽

Chlamydomonas Reinhardtii ◽

Time Course ◽

Nitrogen Starvation ◽

Morphological Changes ◽

Culture Conditions ◽

Homogeneous Material ◽

Term Survival ◽

Thin Sections

Gametogenesis in Chlamydomonas reinhardtii has been studied in mating-type plus cells utilizing several different culture conditions, all of which are shown to depend on the depletion of nitrogen from the medium, and the fine structure of gametes prepared under these conditions has been compared by using thin sections of fixed materials. We document alterations in ribosome levels, in chromatin morphology, in starch levels, in the organization of chloroplast membranes, and in the appearance of nuclear envelope and endoplasmic reticulum membranes during gametogenesis. We also noted the acquisition of two new organelles: a mating structure (Friedman, L., A. L. Colwin, and L. H. Colwin. 1968. j. cell Sci. 3:115-128; goodenough, U. W., and R. L. Weiss. 1975. J. Cell Biol. 67:623-637), and Golgi-derived vesicles containing a homogeneous material. We chart the time course of these morphological changes during synchronous gametogenesis. We note that many of these changes may represent adjustments to nitrogen starvation rather than direct features of gametic differentiation, and we also document that cells can differentiate so that they survive conditions of nitrogen starvation for many weeks after they become gametes. We conclude that metabolic alterations, the acquisition of mating ability, and the preparation for long-term survival are all elicited in this organism by nitrogen withdrawal, and we discuss how the various structural alterations observed in this study may relate to these three interrelated avenues of cellular differentiation.

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Growth responses of seedlings of two neotropical pioneer species to simulated forest gap environments

Journal of Tropical Ecology ◽

10.1017/s0266467499001200 ◽

1999 ◽

Vol 15 (6) ◽

pp. 827-839 ◽

Cited By ~ 29

Author(s):

J. W. Dalling ◽

C. E. Lovelock ◽

S. P. Hubbell

Keyword(s):

Leaf Area ◽

Time Course ◽

Light Quality ◽

Superior Performance ◽

Leaf Biomass ◽

Pioneer Species ◽

Gap Size ◽

Growth Responses ◽

Net Assimilation ◽

Using Data

Traditional shade house experiments that expose plants to relatively uniform irradiance and light quality are inadequate to characterize the morphological, allocational and physiological plasticity that seedlings show to different gap environments. Here the design of a pot experiment is described that simulates the daily time course of irradiance and light quality in idealized gaps of six different sizes. Differences in response to gap size are illustrated using data from two pioneer species, Ochroma pyramidale, which recruits exclusively in large gaps and clearings, and Luehea seemannii, which colonizes small branchfall gaps as well as large gaps. Ochroma outperformed Luehea in relative growth rate in all except the smallest simulated gap size. Ochroma's superior performance in the larger gaps could be attributed to a larger proportional investment in leaf biomass (i.e. a higher leaf area ratio, LAR), and higher photosynthetic rates both on a leaf area and leaf mass basis. In the smallest simulated gaps LAR was not significantly different between the species, but Ochroma maintained a higher net assimilation rate. These results fail to support the suggestion that gap partitioning among pioneer species arises directly from morphological and biochemical specialization to particular gap light environments. Instead, it is suggested that partitioning may result from a trade-off between seedling growth and mortality determined by species allocational patterns and mediated by interactions with herbivores and pathogens.

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