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161.
We present a detailed study of the extrusion of an imperfect palindrome, derived from the terminal regions of vaccinia virus DNA and contained in a superhelical plasmid, into a cruciform containing bulged bases. We monitor the course of extrusion by two-dimensional gel electrophoresis experiments as a function of temperature and linking number. We find that extrusion pauses at partially extruded states as negative superhelicity increases. To understand the course of extrusion with changes in linking number, DeltaLk, we present a rigorous semiempirical statistical mechanical analysis that includes complete coupling between DeltaLk, cruciform extrusion, formation of extrahelical bases, and temperature-dependent denaturation. The imperfections in the palindrome are sequentially incorporated into the cruciform arms as hairpin loops, single unpaired bases, and complex local regions containing several unpaired bases. We analyze the results to determine the free energies, enthalpies and entropies of formation of all local structures involved in extrusion. We find that, for each unpaired structure, the DeltaG, DeltaH and DeltaS of formation are all approximately proportional to the number of unpaired bases contained therein. This surprising result holds regardless of the arrangement or composition of unpaired bases within a particular structure. Imperfections have major effects on the overall energetics of cruciform extrusion and on the course of this transition. In particular, the extent of the DeltaLk change necessary to extrude an imperfect palindrome is considerably greater than that required for extrusion of the underlying perfect palindrome. Our analysis also suggests that, at higher temperatures, significant denaturation at the base of an imperfect cruciform can successfully compete with extension of the cruciform arms. 相似文献
162.
Development of ribozymes that target stathmin, a major regulator of the mitotic spindle 总被引:10,自引:0,他引:10
Stathmin is a major cytosolic phosphoprotein that plays an important role in the control of cellular proliferation by regulating the dynamics of the microtubules that make up the mitotic spindle. Because stathmin is expressed at high levels in all human cancers, it is an attractive molecular target for anticancer interventions. We had shown previously that antisense stathmin inhibition results in marked abrogation of the transformed phenotype of leukemic cells in vitro and in vivo. Unlike the antisense approach, ribozymes can catalytically cleave several molecules of target RNA. This may provide a more efficient strategy for downregulating genes, such as stathmin, that are expressed at very high levels in cancer cells. We designed several antistathmin hammerhead ribozymes and tested their cleavage activity against short synthetic stathmin RNA substrates. In vitro cleavage studies demonstrated site-specific cleavage of stathmin RNA that was dependent on ribozyme concentration and duration of exposure to ribozyme. The most active antistathmin ribozyme was capable of cleaving >90% stathmin RNA in a catalytic manner, cleaving multiple substrate molecules per ribozyme molecule. We also demonstrated that the designed antistathmin ribozymes are capable of selectively cleaving native stathmin RNA in a mixture of total RNA isolated from leukemic cells. These antistathmin ribozymes may provide a novel and effective form of gene therapy that may be applicable to a wide variety of human cancers. 相似文献
163.
164.
Our understanding of eukaryotic protein folding in the endoplasmic reticulum has increased enormously over the last 5 years. In this review, we summarize some of the major research themes that have captivated researchers in this field during the last years of the 20th century. We follow the path of a typical protein as it emerges from the ribosome and enters the reticular environment. While many of these events are shared between different polypeptide chains, we highlight some of the numerous differences between proteins, between cell types, and between the chaperones utilized by different ER glycoproteins. Finally, we consider the likely advances in this field as the new century unfolds and we address the prospect of a unified understanding of how protein folding, degradation, and translation are coordinated within a cell. 相似文献
165.
166.
Silke Winkelmann Martin Klar Craig Benham Ak Prashanth Sandra Goetze Angela Gluch Juergen Bode 《Briefings in Functional Genomics and Prot》2006,5(1):24-31
The conventional string-based bioinformatic methods of genomic sequence analysis are often insufficient to identify DNA regulatory elements, since many of these do not have a recognizable motif. Even in case a sequence pattern is known to be associated with an element it may only partially mediate its function. This suggests that properties not correlated with the details of base sequence contribute to regulation. One of these attributes is the DNA strand-separation potential, known as SIDD (stress-induced duplex destabilization) which facilitates the access of tracking proteins and the formation of local secondary structures. Using the type 1 interferon gene cluster as a paradigm, we demonstrate that the imprints in a SIDD profile coincide with chromatin domain borders and with DNAse I hypersensitive sites to which regulatory potential could be assigned. The approach permits the computer-guided identification of yet unknown, mostly remote sites and the design of artificial elements with predictable properties for multiple applications. 相似文献
167.
Promoter prediction and annotation of microbial genomes based on DNA sequence and structural responses to superhelical stress 总被引:1,自引:0,他引:1
Background
In our previous studies, we found that the sites in prokaryotic genomes which are most susceptible to duplex destabilization under the negative superhelical stresses that occur in vivo are statistically highly significantly associated with intergenic regions that are known or inferred to contain promoters. In this report we investigate how this structural property, either alone or together with other structural and sequence attributes, may be used to search prokaryotic genomes for promoters. 相似文献168.
169.
Effects of climate change on nitrogen dynamics in upland soils. 1. A transplant approach 总被引:6,自引:0,他引:6
Philip Ineson Kenneth Taylor Anthony F. Harrison Janet Poskitt David G. Benham Edward Tipping† Colin Woof† 《Global Change Biology》1998,4(2):143-152
The impact of climate change on N leaching from hill land plant/soil systems was investigated using a transplant technique involving the movement of intact lysimeter cores of three contrasting soil types down an altitudinal gradient at Great Dun Fell, Cumbria. Air and soil temperatures and precipitation were monitored at four elevations down an altitudinal transect using automatic weather stations for a period of two years. The altitudinal sequence of air temperature followed the anticipated pattern, providing mean annual temperatures at the four locations of 3.4, 5.0, 6.3 and 8.1 °C. Lapse rates of both mean air and soil temperatures over the altitudinal range 171–845 m were 6.6 (1993) and 7.0 °C km–1 (1994). Soil monthly temperature gradients for a particular soil type for each of the two years showed a seasonal range of 6.0 and 7.4 °C km–1, respectively, and for air temperature of 4.3 and 3.1 °C km–1. Precipitation gradients showed the expected general increase with altitude, but were less predictable. Inorganic nitrogen leaching was studied in lysimeter leachates with climatic amelioration resulting in dramatic reductions in leachate nitrate concentrations and associated total concentrations of inorganic nitrogen. Decreases in leachate nitrate concentrations were observed for all three soil types studied. Soils receiving supplemented rainfall also showed decreased N concentrations, suggesting that temperature was the main controlling factor responsible for the observed reductions. Increased N uptake by the vegetation, in response to the increases in temperature, is considered to be critical in controlling soil solution chemistry at these sites. 相似文献
170.
Craig J. Benham 《Biopolymers》1983,22(11):2477-2495
This paper analyzes the elastic equilibrium conformations of duplex DNA constrained by the constancy of its molecular linking number, Lk. The DNA is regarded as having the mechanical properties of a homogeneous, linearly elastic substance with symmetric cross section. Integral representations of the writhing number Wr and of Lk are developed, in terms of which the equilibria are given as solutions to an isoperimetric problem. It is shown that the Euler angles defining equilibrium conformations must obey equations identical to those governing unconstrained equilibria. A scaling law is developed stating that molecules supercoiled the same amount ΔLk will have geometrically similar elastic equilibria regardless of their length. Thus, comparisons among molecules of properties related to their large-scale tertiary structure should be referred to differences in ΔLk rather than to their superhelix densities. Specific conditions on the elastic equilibrium conformations are developed that are necessary for ring closure. The equilibrium superhelical conformations accessible to closed-ring molecules are shown to approximate toroidal helices. Questions relating to the stability and nonuniqueness of equilibria are treated briefly. A comparison is made between these toroidal conformations and interwound configurations, which are shown to be stable, although they are not equilibria in the present sense. It is suggested that entropic factors are responsible for favouring the toroidal conformation in solution. 相似文献