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181.
Rute ST Martins Laurence AM Deloffre Constantinos C Mylonas Deborah M Power Adelino VM Canário 《Reproductive biology and endocrinology : RB&E》2007,5(1):19
Background
DAX1 (NR0B1), a member of the nuclear receptors super family, has been shown to be involved in the genetic sex determination and in gonadal differentiation in several vertebrate species. In the aquaculture fish European sea bass, Dicentrarchus labrax, and in the generality of fish species, the mechanisms of sex determination and differentiation have not been elucidated. The present study aimed at characterizing the European DAX1 gene and its developmental expression at the mRNA level. 相似文献182.
183.
High copy number of highly similar mariner-like transposons in planarian (Platyhelminthe): evidence for a trans-phyla horizontal transfer 总被引:8,自引:2,他引:6
Garcia-Fernandez J; Bayascas-Ramirez JR; Marfany G; Munoz-Marmol AM; Casali A; Baguna J; Salo E 《Molecular biology and evolution》1995,12(3):421-431
Several DNA sequences similar to the mariner element were isolated and
characterized in the platyhelminthe Dugesia (Girardia) tigrina. They were
1,288 bp long, flanked by two 32 bp-inverted repeats, and contained a
single 339 amino acid open-reading frame (ORF) encoding the transposase.
The number of copies of this element is approximately 8,000 per haploid
genome, constituting a member of the middle- repetitive DNA of Dugesia
tigrina. Sequence analysis of several elements showed a high percentage of
conservation between the different copies. Most of them presented an intact
ORF and the standard signals of actively expressed genes, which suggests
that some of them are or have recently been functional transposons. The
high degree of similarity shared with other mariner elements from some
arthropods, together with the fact that this element is undetectable in
other planarian species, strongly suggests a case of horizontal transfer
between these two distant phyla.
相似文献
184.
Assessing horizontal transfer of nifHDK genes in eubacteria: nucleotide sequence of nifK from Frankia strain HFPCcI3 总被引:2,自引:1,他引:1
Hirsch AM; McKhann HI; Reddy A; Liao J; Fang Y; Marshall CR 《Molecular biology and evolution》1995,12(1):16-27
The structural genes for nitrogenase, nifK, nifD, and nifH, are crucial for
nitrogen fixation. Previous phylogenetic analysis of the amino acid
sequence of nifH suggested that this gene had been horizontally transferred
from a proteobacterium to the gram-positive/cyanobacterial clade, although
the confounding effects of paralogous comparisons made interpretation of
the data difficult. An additional test of nif gene horizontal transfer
using nifD was made, but the NifD phylogeny lacked resolution. Here nif
gene phylogeny is addressed with a phylogenetic analysis of a third and
longer nif gene, nifK. As part of the study, the nifK gene of the key taxon
Frankia was sequenced. Parsimony and some distance analyses of the nifK
amino acid sequences provide support for vertical descent of nifK, but
other distance trees provide support for the lateral transfer of the gene.
Bootstrap support was found for both hypotheses in all trees; the nifK data
do not definitively favor one or the other hypothesis. A parsimony analysis
of NifH provides support for horizontal transfer in accord with previous
reports, although bootstrap analysis also shows some support for vertical
descent of the orthologous nifH genes. A wider sampling of taxa and more
sophisticated methods of phylogenetic inference are needed to understand
the evolution of nif genes. The nif genes may also be powerful phylogenetic
tools. If nifK evolved by vertical descent, it provides strong evidence
that the cyanobacteria and proteobacteria are sister groups to the
exclusion of the firmicutes, whereas 16S rRNA sequences are unable to
resolve the relationships of these three major eubacterial lineages.
相似文献
185.
MANO SABARATN AM 《The Journal of eukaryotic microbiology》1971,18(1):141-146
SYNOPSIS. Gregarina fernandoi n. sp. is a eugregarine. Its structure, development and life history in the gut of the cockroach Pycnoscelus surinamensis are described. It is named as a new species on the basis of its size, nuclear structure, structure and form of the gametocyst and oocyst. Observations were made on the different stages of the parasite and related to the pH of the gut. In the ceca, pH 4.5–5, the parasite was in its early stages of development, in the midgut, pH 6.5–7, it was in syzygy and in the rectum, pH 7.5–8, gametocysts were found. 相似文献
186.
187.
Short repetitive sequences in green algal mitochondrial genomes: potential roles in mitochondrial genome evolution 总被引:4,自引:2,他引:2
Current data on green algal mitochondrial genomes suggest an unexpected
dichotomy within the group with respect to genome structure, organization,
and sequence affiliations. The present study suggests that there is a
correlation between this dichotomy on one hand and the differences in the
abundance, base composition, and distribution of short repetitive sequences
we observed among green algal mitochondrial genomes on the other. It is
conceivable that the accumulation of GC- rich short repeated sequences in
the Chlamydomonas-like but not Prototheca-like mitochondrial genomes might
have triggered evolutionary events responsible for the distinct series of
evolutionary changes undergone by the two green algal mitochondrial
lineages. The similarity in base composition, nucleotide sequence,
abundance, and mode of organization we observed between the short
repetitive sequences present in Chlamydomonas-like mitochondrial genomes on
one hand and fungal and vertebrate homologs on the other might extend to
some of the roles that the short repetitive sequences have been shown to
have in the latter. Potential involvements we propose for the short
repetitive sequences in the evolution of Chlamydomonas-like mitochondrial
genomes include fragmentation and scrambling of the ribosomal-RNA-coding
regions, extensive gene rearrangements, coding-region deletions, surrogate
origins of replication, and chromosomal linearization.
相似文献
188.
A. terreus isolates isolated from some bakery products, corn and rice were found to be able to produce territrems. 90% of theA. terreus isolated from bakery products were able to produce territrem A, with a mean of 0.09 ppm, while 80% ofA. terreus isolates produce territrem B with a mean of 0.24 ppm. On the other hand 31.8% of the isolates ofA. terreus from corn were able to produce territrem A with a mean of 0.44 ppm. ConcerningA. terreus isolates from rice, 66.7% were found to produce territrem A, with a mean of 5.28 ppm, and 77.8% of the isolates produced
territrem B with a mean of 1.79 ppm. 相似文献
189.
Parissenti AM Villeneuve D Kirwan-Rhude A Busch D 《Journal of cellular physiology》1999,178(2):216-226
Protein kinase C is known to play a role in cell cycle regulation in both lower and higher eucaryotic cells. Since mutations in yeast proteins involved in cell cycle regulation can often be rescued by the mammalian homolog and since significant conservation exists between PKC-signalling pathways in yeast and mammalian cells, cell cycle regulation by mammalian PKC isoforms may be effectively studied in a simpler genetically-accessible model system such as Saccharomyces cerevisiae. With this objective in mind, we transfected S. cerevisiae cells with a plasmid (pYECepsilon) coding for the expression of murine protein kinase C epsilon (PKCepsilon) under the control of a galactose-inducible promoter. Unlike mock-transfected cells, yeast cells transformed with pYECepsilon expressed, in a galactose-dependent manner, an 89 kDa protein that was recognized by a human PKCepsilon antibody. Extracts from these pYECepsilon-transfected cells could phosphorylate a PKCepsilon substrate peptide in a phospholipid/phorbol ester-dependent manner. Moreover, this catalytic activity could be inhibited by a fusion protein in which the regulatory domain of murine PKCepsilon was fused in frame with GST (GST-Repsilon), further confirming the successful expression of murine PKCepsilon. Induction of PKCepsilon expression by galactose in cells transformed with pYECepsilon increased Ca++ uptake by the cells approximately 5-fold and resulted in a dramatic inhibition of cell growth in glycerol. However, when glucose was used as the carbon source, PKCepsilon expression had no effect on cell growth. This was in contrast to what was observed upon bovine PKCalpha or PKCbeta-I expression in yeast, where expression of these PKC isoforms strongly and moderately inhibited growth in glucose, respectively. Visualization of the cells by phase contrast microscopy indicated that murine PKCepsilon expression in the presence of glycerol resulted in a significant increase in the number of yeast cells exhibiting very small buds. Since overall growth of the cells was dramatically decreased, the data suggests that PKCepsilon expression potently inhibits the progression of yeast cells through the cell cycle after the initiation of budding. In addition, a small amount of the PKCepsilon-expressing yeast cells (1-2%) exhibited gross alterations in cell morphology and defects in both chromosome segregation and septum formation. This suggests that for those cells which do complete DNA synthesis, murine PKCepsilon expression may nevertheless inhibit yeast cell growth by retarding and/or imparing cell division. Taken together, the data suggests murine PKCepsilon expression potently reduces the growth of yeast cells in a carbon source-dependent fashion by affecting progression through multiple points within the cell cycle. This murine PKCepsilon-expressing yeast strain may serve as a very useful tool in the elucidation of mechanism(s) by which external environmental signals (possibly through specific PKC isoforms) regulate cell cycle progression in both yeast and mammalian cells. 相似文献
190.