The Light on the Leaves

Author(s):  
David R. Dalton

As noted earlier in the general description of the plant cell, there is a site at which photosynthesis, the process which allows plants to capture sunlight and convert it into energy, occurs. It is this process which has produced oxygen on the planet, food for herbivores, and the cool green hills of Earth we enjoy today. The capture of sunlight allows the grape vine to grow and produce fruit. Of course, while the discussion of the “light reactions” (capture of sunlight) and the subsequent so-called “dark reactions” (producing carbohydrates) is necessarily brief here, it is, nonetheless, an exciting story. We are only now beginning to understand a little of it. The earlier picture (Figure 7.1) of the plant cell is repeated here (Figure 9.1) so that the position of the chloroplast is seen. Refer to page 24 for a discussion of the numbered items. As the leaves begin to develop alongside the apical meristem, proplastids, which are present in the meristematic regions of the plant, are formed. Proplastids grow into plas¬tids (such as amyloplasts and chloroplasts) as they mature in different ways dictated by the plant’s DNA. Some plastids (e.g., chloroplasts) carry pigments, discussed more fully below, that allow them to carry out photosynthesis. Others are used for storage of fat, starch (amyloplasts) or specialized proteins. Still other plastids are used to synthesize specialized compounds needed to form different tissues or to produce compounds for protection (e.g., tannins). Each plastid builds multiple copies of its DNA as it grows. If it is growing rapidly, it makes more genome copies than if it is growing slowly. The genes, ignoring epigenetic (literally “above the gene”) and postgenetic (literally “after the gene”) modifications, about which we still have much to learn, encode plastid proteins, the regulation of whose expression controls differentiation and thus which plastid is eventually formed. However, despite the differentiation of plastids, it appears that many plastids remain connected to each other by tubes called stromules through which proteins can be exchanged.

1985 ◽  
Vol 5 (4) ◽  
pp. 649-658
Author(s):  
G M Veldman ◽  
S Lupton ◽  
R Kamen

Sequences that comprise the 244-base-pair polyomavirus enhancer region are also required in cis for viral DNA replication (Tyndall et al., Nucleic Acids Res. 9:6231-6250, 1981). We have studied the relationship between the sequences that activate replication and those that enhance transcription in two ways. One approach, recently described by de Villiers et al. (Nature [London], 312:242-246, 1984), in which the polyomavirus enhancer region was replaced with other viral or cellular transcriptional enhancers suggested that an enhancer function is required for polyomavirus DNA replication. The other approach, described in this paper, was to analyze a series of deletion mutants that functionally dissect the enhancer region and enabled us to localize four sequence elements in this region that are involved in the activation of replication. These elements, which have little sequence homology, are functionally redundant. Element A (nucleotides 5108 through 5130) was synthesized as a 26-mer with XhoI sticky ends, and one or more copies were introduced into a plasmid containing the origin of replication, but lacking the enhancer region. Whereas one copy of the 26-mer activated replication only to 2 to 5% of the wild-type level, two copies inserted in either orientation completely restored replication. We found that multiple copies of the 26-mer were also active as a transcriptional enhancer by measuring the beta-globin mRNA levels expressed from a plasmid that contained either the polyomavirus enhancer or one or more copies of the 26-mer inserted in a site 3' to the beta-globin gene. We observed a correlation between the number of inserted 26-mers and the level of beta-globin RNA expression.


1977 ◽  
Vol 59 (3) ◽  
pp. 388-390 ◽  
Author(s):  
Barbara B. Lippincott ◽  
Mariamne H. Whatley ◽  
James A. Lippincott

1985 ◽  
Vol 5 (4) ◽  
pp. 649-658 ◽  
Author(s):  
G M Veldman ◽  
S Lupton ◽  
R Kamen

Sequences that comprise the 244-base-pair polyomavirus enhancer region are also required in cis for viral DNA replication (Tyndall et al., Nucleic Acids Res. 9:6231-6250, 1981). We have studied the relationship between the sequences that activate replication and those that enhance transcription in two ways. One approach, recently described by de Villiers et al. (Nature [London], 312:242-246, 1984), in which the polyomavirus enhancer region was replaced with other viral or cellular transcriptional enhancers suggested that an enhancer function is required for polyomavirus DNA replication. The other approach, described in this paper, was to analyze a series of deletion mutants that functionally dissect the enhancer region and enabled us to localize four sequence elements in this region that are involved in the activation of replication. These elements, which have little sequence homology, are functionally redundant. Element A (nucleotides 5108 through 5130) was synthesized as a 26-mer with XhoI sticky ends, and one or more copies were introduced into a plasmid containing the origin of replication, but lacking the enhancer region. Whereas one copy of the 26-mer activated replication only to 2 to 5% of the wild-type level, two copies inserted in either orientation completely restored replication. We found that multiple copies of the 26-mer were also active as a transcriptional enhancer by measuring the beta-globin mRNA levels expressed from a plasmid that contained either the polyomavirus enhancer or one or more copies of the 26-mer inserted in a site 3' to the beta-globin gene. We observed a correlation between the number of inserted 26-mers and the level of beta-globin RNA expression.


Author(s):  
Mariangela Iannello ◽  
Stefano Bettinazzi ◽  
Sophie Breton ◽  
Fabrizio Ghiselli ◽  
Liliana Milani

Abstract Mitochondrial DNA (mtDNA) is present in multiple copies within an organism. Since these copies are not identical, a single individual carries a heterogeneous population of mtDNAs, a condition known as heteroplasmy. Several factors play a role in the dynamics of the within-organism mtDNA population: among them genetic bottlenecks, selection, and strictly maternal inheritance are known to shape the levels of heteroplasmy across mtDNAs. In Metazoa, the only evolutionarily stable exception to the strictly maternal inheritance of mitochondria is the doubly uniparental inheritance (DUI), reported in 100+ bivalve species. In DUI species there are two highly divergent mtDNA lineages, one inherited through oocyte mitochondria (F-type) and the other through sperm mitochondria (M-type). Having both parents contributing to the mtDNA pool of the progeny makes DUI a unique system to study the dynamics of mtDNA populations. Since in bivalves the spermatozoon has few mitochondria (4-5), M-type mtDNA faces a tight bottleneck during embryo segregation, one of the narrowest mitochondrial bottlenecks investigated so far. Here, we analyzed the F- and M-type mtDNA variability within individuals of the DUI species Ruditapes philippinarum, and we investigated for the first time the effects of such a narrow bottleneck affecting mtDNA populations. As a potential consequence of this narrow bottleneck, the M-type mtDNA shows a large variability in different tissues, a condition so pronounced that it leads to genotypes from different tissues of the same individual not to cluster together. We believe such results may help understanding the effect of low population size on mtDNA bottleneck.


1970 ◽  
Vol 23 (2) ◽  
pp. 479 ◽  
Author(s):  
MG Mullins ◽  
Daphne J Osborne

The inflorescences of woody grape vine cuttings usually atrophy if bud burst precedes emergence of adventitious roots (Mullins 1967). Roots are a site of cytokinin synthesis (Kende 1964; Itai and Vaadia 1965), and the ascending sap of vines is rich in endogenous cytokinin (Loeffler and Van Over beek 1964; Nitsch and Nitsch 1965; Skene and Kerridge 1967). The inflorescences of vine cuttings are retained and continue to grow if roots are initiated before bud burst, and the inflorescences of non-rooted cuttings are retained when treated with synthetic cytokinins (Mullins 1967).


2016 ◽  
Vol 95 ◽  
pp. 44-49 ◽  
Author(s):  
Kazuhiro Toyoda ◽  
Sachiyo Yao ◽  
Mai Takagi ◽  
Maki Uchioki ◽  
Momiji Miki ◽  
...  

2010 ◽  
Vol 192 (10) ◽  
pp. 2482-2490 ◽  
Author(s):  
J. S. Hankins ◽  
H. Denroche ◽  
G. A. Mackie

ABSTRACT CspA, a small protein that is highly induced by cold shock, is encoded by a monocistronic mRNA of 428 nucleotides (nt) whose half-life and abundance are greatly increased following cold shock. We show here that in vitro cspA mRNA can bind multiple copies of Hfq, a hexameric Sm-like protein which promotes a variety of RNA-RNA interactions. Binding of the first Hfq hexamer occurs with an apparent Kd (dissociation constant) of <40 nM; up to seven additional hexamers can bind sequentially at higher concentrations. Known ligands of Hfq, including the small regulatory RNA, RyhB, compete with cspA mRNA. Several experiments suggest that the first binding site to be occupied by Hfq is located at or near the 3′ end of cspA mRNA. The consequences of limited Hfq binding in vitro include nearly total inhibition of RNase E cleavage at a site ∼35 nt from the 3′ end of the mRNA, stimulation of polyadenylation by poly(A) polymerase 1, and subsequent exonucleolytic degradation by polynucleotide phosphorylase. We propose that Hfq may play a facilitating role in the metabolism of cspA mRNA.


1988 ◽  
Vol 66 (9) ◽  
pp. 1717-1722
Author(s):  
Hinrich Harries ◽  
Felix Bärlocher

The living stems of striped maple (Acer pensylvanicum L.) at two sites in Nova Scotia were found to be covered by a striking pattern of fungal hyphae belonging to Pseudospiropes sp. The fungus colonizes branches or seedlings during their first season, and the density of its coverage increases every year thereafter. The fungus was absent from striped maple at a site near Lake Placid, NY, and there is some evidence that its frequency of occurrence has declined elsewhere in the last few years. A pure culture of the fungus was unable to hydrolyze several plant cell wall polymers. It was able to use simple lipids, however, and its presence increased the erosion of the cutinized layer of striped maple stems. The fungus does not penetrate the stem surface, and its occurrence is not correlated with twig length or volume. It was absent from three sympatric maple species.


Author(s):  
O.L. Krivanek ◽  
J. TaftØ

It is well known that a standing electron wavefield can be set up in a crystal such that its intensity peaks at the atomic sites or between the sites or in the case of more complex crystal, at one or another type of a site. The effect is usually referred to as channelling but this term is not entirely appropriate; by analogy with the more established particle channelling, electrons would have to be described as channelling either through the channels or through the channel walls, depending on the diffraction conditions.


Sign in / Sign up

Export Citation Format

Share Document