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311.
Molecular coevolution among cryptically simple expansion segments of eukaryotic 26S/28S rRNAs 总被引:16,自引:4,他引:12
The set of "expansion segments" of any eukaryotic 26S/28S ribosomal RNA
(rRNA) gene is responsible for the bulk of the difference in length between
the prokaryotic 23S rRNA gene and the eukaryotic 26S/28S rRNA gene. The
expansion segments are also responsible for interspecific fluctuations in
length during eukaryotic evolution. They show a consistent bias in base
composition in any species; for example, they are AT rich in Drosophila
melanogaster and GC rich in vertebrate species. Dot-matrix comparisons of
sets of expansion segments reveal high similarities between members of a
set within any 28S rRNA gene of a species, in contrast to the little or
spurious similarity that exists between sets of expansion segments from
distantly related species. Similarities among members of a set of expansion
segments within any 28S rRNA gene cannot be accounted for by their
base-compositional bias alone. In contrast, no significant similarity
exists within a set of "core" segments (regions between expansion segments)
of any 28S rRNA gene, although core segments are conserved between species.
The set of expansion segments of a 26S/28S gene is coevolving as a unit in
each species, at the same time as the family of 28S rRNA genes, as a whole,
is undergoing continual homogenization, making all sets of expansion
segments from all ribosomal DNA (rDNA) arrays in a species similar in
sequence. Analysis of DNA simplicity of 26S/28S rRNA genes shows a direct
correlation between significantly high relative simplicity factors (RSFs)
and sequence similarity among a set of expansion segments. A similar
correlation exists between RSF values, overall rDNA lengths, and the
lengths of individual expansion segments. Such correlations suggest that
most length fluctuations reflect the gain and loss of simple sequence
motifs by slippage-like mechanisms. We discuss the molecular coevolution of
expansion segments, which takes place against a background of slippage-like
and unequal crossing-over mechanisms of turnover that are responsible for
the accumulation of interspecific differences in rDNA sequences.
相似文献
312.
313.
Partial 18S rRNA sequences of five chelicerate arthropods plus a
crustacean, myriapod, insect, chordate, echinoderm, annelid, and
platyhelminth were compared. The sequence data were used to infer phylogeny
by using a maximum-parsimony method, an evolutionary-distance method, and
the evolutionary-parsimony method. The phylogenetic inferences generated by
maximum-parsimony and distance methods support both monophyly of the
Arthropoda and monophyly of the Chelicerata within the Arthropoda. These
results are congruent with phylogenies based on rigorous cladistic analyses
of morphological characters. Results support the inclusion of the
Arthropoda within a spiralian or protostome coelomate clade that is the
sister group of a deuterostome clade, refuting the hypothesis that the
arthropods represent the "primitive" sister group of a protostome coelomate
clade. Bootstrap analyses and consideration of all trees within 1% of the
length of the most parsimonious tree suggest that relationships between the
nonchelicerate arthropods and relationships within the chelicerate clade
cannot be reliably inferred with the partial 18S rRNA sequence data. With
the evolutionary-parsimony method, support for monophyly of the Arthropoda
is found in the majority of the combinations analyzed if the coelomates are
used as "outgroups." Monophyly of the Chelicerata is supported in most
combinations assessed. Our analyses also indicate that the
evolutionary-parsimony method, like distance and parsimony, may be biased
by taxa with long branches. We suggest that a previous study's inference of
the Arthropoda as paraphyletic may be the result of (a) having two few
arthropod taxa available for analysis and (b) including long-branched taxa.
相似文献
314.
Central processing of inertial sensory information about head attitude and motion in space is crucial for motor control. Vestibular signals are coded relative to a non-inertial system, the head, that is virtually continuously in motion. Evidence for transformation of vestibular signals from head-fixed sensory coordinates to gravity-centered coordinates have been provided by studies of the vestibulo-ocular reflex. The underlying central processing depends on otolith afferent information that needs to be resolved in terms of head translation related inertial forces and head attitude dependent pull of gravity. Theoretical solutions have been suggested, but experimental evidence is still scarce. It appears, along these lines, that gaze control systems are intimately linked to motor control of head attitude and posture. 相似文献
315.
316.
Several and various types of cells contain fine cytoplasmic filaments closely resembling the myofilaments of muscle cells (2, 18, 23, 24). In many of these cells and especially when cultured, it has been demonstrated that some of these filaments react with heavy meromyosin (HMM) in the same way as do the actin filaments of muscle cells (3, 6 7). This suggests that these filaments may be actinoid and form part of a contractile system. As fine intracytoplasmic filaments do occur in lymphatic endothelial cells (2, 14), we undertook an electron microscope investigation of their fine structure and their reaction on incubation with HMM and EDTA. We postulated that lymphatic endothelial cells possess a contractile filamentous system to which these filaments belong. 相似文献
317.
318.
319.
An experimental system was developed in which the majority of all lymphocyte cell-surface proteins, regardless of antigenic specificity, could be cross-linked and redistributed in the membrane to determine whether this would induce a corresponding redistribution of intramembrane particles (IMP). Mouse spleen cells were treated with P-diazoniumphenyl- β-D-lactoside (lac) to modify all exposed cell-surface proteins. Extensive azo- coupling was achieved without significantly reducing cell viability or compromising cellular function in mitogen- or antigen-stimulated cultures. When the lac-modified cell- surface proteins were capped with a sandwich of rabbit antilactoside antibody and fluorescein-goat anti-rabbit Ig, freeze-fracture preparations obtained from these cells revealed no obvious redistribution of IMP on the majority of fracture faces. However, detailed analysis showed a statistically significant 35 percent decrease (P less than 0.01) in average IMP density in the E face of the lac-capped spleen cells compared with control cells, whereas a few E-face micrographs showed intense IMP aggregation. In contrast, there was no significant alteration of P-face IMP densities or distribution. Apparently, the majority of E-face IMP and virtually all P-face IMP densities or distribution. Apparently, the majority of E-face IMP and virtually all P-face IMP do not present accessible antigenic sites on the lymphocyte surface and do not associate in a stable manner with surface protein antigens. This finding suggests that IMP, as observed in freeze-fracture analysis, may not comprise a representative reflection of lymphocyte transmembrane protein molecules and complexes because other evidence establishes: (a) that at least some common lymphocyte surface antigens are indeed exposed portions of transmembrane proteins and (b) that the aggregation of molecules of any surface antigen results in altered organization of contractile proteins at the cytoplasmic face of the membrane. 相似文献
320.