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61.
The genome sequence of the most widely cultivated cacao type and its use to identify candidate genes regulating pod color 总被引:1,自引:0,他引:1
Juan C Motamayor Keithanne Mockaitis Jeremy Schmutz Niina Haiminen Donald Livingstone III Omar Cornejo Seth D Findley Ping Zheng Filippo Utro Stefan Royaert Christopher Saski Jerry Jenkins Ram Podicheti Meixia Zhao Brian E Scheffler Joseph C Stack Frank A Feltus Guiliana M Mustiga Freddy Amores Wilbert Phillips Jean Philippe Marelli Gregory D May Howard Shapiro Jianxin Ma Carlos D Bustamante Raymond J Schnell Dorrie Main Don Gilbert Laxmi Parida David N Kuhn 《Genome biology》2013,14(6):r53
62.
Molecular evolutionary dynamics of cytochrome b in strepsirrhine primates: the phylogenetic significance of third-position transversions 总被引:3,自引:2,他引:1
DNA sequences of the complete cytochrome b gene are shown to contain robust
phylogenetic signal for the strepsirrhine primates (i.e., lemurs and
lorises). The phylogeny derived from these data conforms to other molecular
studies of strepsirrhine relationships despite the fact that uncorrected
nucleotide distances are high for nearly all intrastrepsirrhine
comparisons, with most in the 15%-20% range. Cytochrome b sequences support
the hypothesis that Malagasy lemuriforms and Afro-Asian lorisiforms each
comprise clades that share a sister- group relationship. A study (Adkins
and Honeycutt 1994) of the cytochrome c oxidase subunit II (COII) gene
placed one Malagasy primate (Daubentonia) at the base of the strepsirrhine
clade, thereby suggesting a diphyletic Lemuriformes. The reanalysis of COII
third- position transversions, either alone or in combination with
cytochrome b third-position transversions, however, yields a tree that is
congruent with phylogenetic hypotheses derived from cytochrome b and other
genetic data sets.
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63.
Summary Secretory products of granular and mucous cells in the gill epithelium of the carp, Cyprinus carpio, were distinguished by their cytochemical reactions with peroxidase-labelled lectins and with the galactose oxidase (GO)-Schiff reagents. Secretory products of granular cells reacted with lectins from Triticum vulgaris (WGA), Arachis hypogaea (PNA), Dolichos biflorus (DBA), Glycine max (SAB), and Lotus tetragonolobus (LTA). They also reacted with GO-Schiff reagents. After sialic acid cleavage with HCl, new binding sites for DBA and SBA appeared, suggesting the terminal sequence sialic acid-N-acetylgalactosamine (SA-GalNAc) for the secretion of this cell type. In mucous cells, binding sites for WGA, DBA, and SBA and, after acid hydrolysis, binding sites for PNA and a positive GO-Schiff reaction were detected. The terminal trisaccharide sialic acid-galactose (1-3)-N-acetylgalactosamine (SA-Gal-GalNAc) is proposed for the secretion of mucuous cells. These cytochemical differences are discussed in light of the involvement of both cell types in fish mucus elaboration. 相似文献
64.
The effect of relaxed functional constraints on the photosynthetic gene rbcL in photosynthetic and nonphotosynthetic parasitic plants 总被引:1,自引:0,他引:1
The photosynthetic gene rbcL has been lost or dramatically altered in some
lineages of nonphotosynthetic parasitic plants, but the dynamics of these
events following loss of photosynthesis and whether rbcL has sustained
functionally significant changes in photosynthetic parasitic plants are
unknown. To assess the changes to rbcL associated with the loss of
functional constraints for photosynthesis, nucleotide sequences from
nonparasitic and parasitic plants of Scrophulariales were used for
phylogeny reconstruction and character analysis. Plants in this group
display a broad range of parasitic abilities, from photosynthetic
("hemiparasites") to nonphotosynthetic ("holoparasites"). With the
exception of Conopholis (Orobanchaceae), the rbcL locus is present in all
parasitic plants of Scrophulariales examined. Several holoparasitic genera
included in this study, including Boschniakia, Epifagus, Orobanche, and
Hyobanche, have rbcL pseudogenes. However, the holoparasites Alectra
orobanchoides, Harveya capensis, Harveya purpurea, Lathraea clandestina,
Orobanche corymbosa, O. fasciculata, and Striga gesnerioides have intact
open reading frames (ORFs) for the rbcL gene. Phylogenetic hypotheses based
on rbcL are largely in agreement with those based on sequences of the
nonphotosynthetic genes rps2 and matK and show a single origin of
parasitism, and loss of photosynthesis and pseudogene formation have been
independently derived several times in Scrophulariales. The mutations in
rbcL in nonparasitic and hemiparasitic plants would result in largely
conservative amino acid substitutions, supporting the hypothesis that
functional proteins can experience only a limited range of changes, even in
minimally photosynthetic plants. In contrast, ORFs in some holoparasites
had many previously unobserved missense substitutions at functionally
important amino acid residues, suggesting that rbcL genes in these plants
have evolved under relaxed or altered functional constraints.
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65.
Dissection of cell division processes in the one cell stage Caenorhabditis elegans embryo by mutational analysis
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Gönczy P Schnabel H Kaletta T Amores AD Hyman T Schnabel R 《The Journal of cell biology》1999,144(5):927-946
To identify novel components required for cell division processes in complex eukaryotes, we have undertaken an extensive mutational analysis in the one cell stage Caenorhabditis elegans embryo. The large size and optical properties of this cell permit observation of cell division processes with great detail in live specimens by simple differential interference contrast (DIC) microscopy. We have screened an extensive collection of maternal-effect embryonic lethal mutations on chromosome III with time-lapse DIC video microscopy. Using this assay, we have identified 48 mutations in 34 loci which are required for specific cell division processes in the one cell stage embryo. We show that mutations fall into distinct phenotypic classes which correspond, among others, to the processes of pronuclear migration, rotation of centrosomes and associated pronuclei, spindle assembly, chromosome segregation, anaphase spindle positioning, and cytokinesis. We have further analyzed pronuclear migration mutants by indirect immunofluorescence microscopy using antibodies against tubulin and ZYG-9, a centrosomal marker. This analysis revealed that two pronuclear migration loci are required for generating normal microtubule arrays and four for centrosome separation. All 34 loci have been mapped by deficiencies to distinct regions of chromosome III, thus paving the way for their rapid molecular characterization. Our work contributes to establishing the one cell stage C. elegans embryo as a powerful metazoan model system for dissecting cell division processes. 相似文献
66.
J Topczewski D S Sepich D C Myers C Walker A Amores Z Lele M Hammerschmidt J Postlethwait L Solnica-Krezel 《Developmental cell》2001,1(2):251-264
Mutations in the zebrafish knypek locus impair gastrulation movements of convergent extension that narrow embryonic body and elongate it from head to tail. We demonstrate that knypek regulates cellular movements but not cell fate specification. Convergent extension movement defects in knypek are associated with abnormal cell polarity, as mutant cells fail to elongate and align medio-laterally. Positional cloning reveals that knypek encodes a member of the glypican family of heparan sulfate proteoglycans. Double mutant and overexpression analyses show that Knypek potentiates Wnt11 signaling, mediating convergent extension. These studies provide experimental and genetic evidence that glypican Knypek acts during vertebrate gastrulation as a positive modulator of noncanonical Wnt signaling to establish polarized cell behaviors underlying convergent extension movements. 相似文献
67.
Alternative splicing and protein function 总被引:1,自引:0,他引:1
AD?Neverov II?Artamonova RN?Nurtdinov D?Frishman MS?GelfandEmail author AA?Mironov 《BMC bioinformatics》2005,6(1):266
Background
Alternative splicing is a major mechanism of generating protein diversity in higher eukaryotes. Although at least half, and probably more, of mammalian genes are alternatively spliced, it was not clear, whether the frequency of alternative splicing is the same in different functional categories. The problem is obscured by uneven coverage of genes by ESTs and a large number of artifacts in the EST data. 相似文献68.
Rhinn M Lun K Amores A Yan YL Postlethwait JH Brand M 《Mechanisms of development》2003,120(8):919-936
The organizer at the midbrain-hindbrain boundary (MHB) forms at the interface between Otx2 and Gbx2 expressing cell populations, but how these gene expression domains are set up and integrated with the remaining machinery controlling MHB development is unclear. Here we report the isolation, mapping, chromosomal synteny and spatiotemporal expression of gbx1 and gbx2 in zebrafish. We focus in particular on the expression of these genes during development of the midbrain-hindbrain territory. Our results suggest that these genes function in this area in a complex fashion, as evidenced by their highly dynamic expression patterns and relation to Fgf signaling. Analysis of gbx1 and gbx2 expression during formation of the MHB in mutant embryos for pax2.1, fgf8 and pou2 (noi, ace, spg), as well as Fgf-inhibition experiments, show that gbx1 acts upstream of these genes in MHB development. In contrast, gbx2 activation requires ace (fgf8) function, and in the hindbrain primordium, also spg (pou2). We propose that in zebrafish, gbx genes act repeatedly in MHB development, with gbx1 acting during the positioning period of the MHB at gastrula stages, and gbx2 functioning after initial formation of the MHB, from late gastrulation stages onwards. Transplantation studies furthermore reveal that at the gastrula stage, Fgf8 signals from the hindbrain primordium into the underlying mesendoderm. Apart from the general involvement of gbx genes in MHB development reported also in other vertebrates, these results emphasize that early MHB development can be divided into multiple steps with different genetic requirements with respect to gbx gene function and Fgf signaling. Moreover, our results provide an example for switching of a specific gene function of gbx1 versus gbx2 between orthologous genes in zebrafish and mammals. 相似文献
69.
Developmental genetic basis for the evolution of pelvic fin loss in the pufferfish Takifugu rubripes
Tanaka M Hale LA Amores A Yan YL Cresko WA Suzuki T Postlethwait JH 《Developmental biology》2005,281(2):227-239
Paired appendages were a key developmental innovation among vertebrates and they eventually evolved into limbs. Ancient developmental control systems for paired fins and limbs are broadly conserved among gnathostome vertebrates. Some lineages including whales, some salamanders, snakes, and many ray-fin fish, independently lost the pectoral, pelvic, or both appendages over evolutionary time. When different taxa independently evolve similar developmental morphologies, do they use the same molecular genetic mechanisms? To determine the developmental genetic basis for the evolution of pelvis loss in the pufferfish Takifugu rubripes (fugu), we isolated fugu orthologs of genes thought to be essential for limb development in tetrapods, including limb positioning (Hoxc6, Hoxd9), limb bud initiation (Pitx1, Tbx4, Tbx5), and limb bud outgrowth (Shh, Fgf10), and studied their expression patterns during fugu development. Results showed that bud outgrowth and initiation fail to occur in fugu, and that pelvis loss is associated with altered expression of Hoxd9a, which we show to be a marker for pelvic fin position in three-spine stickleback Gasterosteus aculeatus. These results rule out changes in appendage outgrowth and initiation genes as the earliest developmental defect in pufferfish pelvic fin loss and suggest that altered Hoxd9a expression in the lateral mesoderm may account for pelvis loss in fugu. This mechanism appears to be different from the mechanism for pelvic loss in stickleback, showing that different taxa can evolve similar phenotypes by different mechanisms. 相似文献
70.
The components of hard tissues including dentin, enamel, cementum, bone and other calcified deposits, and mature and immature collagen pose problems for identification in routine hematoxylin and eosin (H & E) stained sections. Use of combinations of stains can demonstrate the components of hard tissues and soft tissues distinctly. We assessed the efficacy of the Verde Luz-orange G-acid fuchsin (VOF) stain for differentiating hard and soft connective tissues and compared results with other histochemical staining techniques. Eighty tissue sections comprising developing tooth (30), ossifying fibroma (30) and miscellaneous pathologies (20) expected to contain varying types of calcified tissues were stained with H & E, VOF, and Masson's trichrome (MT). In developing tooth, VOF demonstrated better differentiation of hard tissues, while it was comparable to MT for ossifying fibroma and miscellaneous pathologies. The intensity of staining was greater with VOF than with the other stains studied. VOF stains hard tissue components distinctly and gives good contrast with the surrounding connective tissue. VOF is comparable to MT, but has added advantages including single step staining, rapid and easy procedures, and it distinguishes the maturity of the tissues. 相似文献