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931.
Recently, the sika deer, Cervus nippon Temminck, population has increased on Mt Ohdaigahara, central Japan. The dwarf bamboo, Sasa nipponica Makino et Shibata, is a primary forage plant for sika deer in this area. To demonstrate the characteristics of S. nipponica grassland, especially as summer forage for sika deer, the habitat use intensity of sika deer was estimated by fecal densities, and biomass, growth rate, removal by deer and crude protein content were examined. Sika deer utilized the S.nipponica grassland on Mt Ohdaigahara during summer when the biomass, growth rate and crude protein content of S. nipponica were high. The recent increase in the deer population seems to be partly due to S.nipponica grassland being a favorable summer habitat. 相似文献
932.
Dual amino acid-selective and site-directed stable-isotope labeling of the human c-Ha-Ras protein by cell-free synthesis 总被引:4,自引:4,他引:0
933.
Elizabeth A. Register Ruth Yokoyama Shozo Yokoyama 《Journal of molecular evolution》1994,39(3):268-273
Vertebrate opsins are divided into four major groups: RH1 (rhodopsins), RH2 (rhodopsinlike with various absorption sensitivities), SWS (short-wavelength sensitive), and LWS/MWS (long and middle-wavelength sensitive) groups. The green opsin genes (g101
Af
and g101
Af
) in a Mexican characin Astyanax fasciatus belong to the LWS/MWS group, whereas those in goldfish belong to the RH2 group (Yokoyama 1994, Mol Biol Evol 11:32–39). A newly isolated opsin gene (rh11
Af
) from A. fasciatus contains five exons and four introns, spanning 4.2 kilobases from start to stop codons. This gene is most closely related to the two green opsin genes of goldfish and belongs to the RH2 group. In the LWS/MWS group, gene duplication of the ancestral red and green opsin genes predates the speciation between A. fasciatus and goldfish, suggesting that goldfish also has an additional gene which is orthologous to g101
Af
and g103
Af
.Correspondence to: S. Yokoyama 相似文献
934.
Yutaka Muto Kazuhiko Yamasaki Yutaka Ito Shunsuke Yajima Haruhiko Masaki Takeshi Uozumi Markus Wälchli Susumu Nishimura Tatsuo Miyazawa Shigeyuki Yokoyama 《Journal of biomolecular NMR》1993,3(2):165-184
Summary All the backbone 1H and 15N magnetic resonances (except for Pro residues) of the GDP-bound form of a truncated human c-Ha-ras proto-oncogene product (171 amino acid residues, the Ras protein) were assigned by 15N-edited two-dimensional NMR experiments on selectively 15N-labeled Ras proteins in combination with three-dimensional NMR experiments on the uniformly 15N-labeled protein. The sequence-specific assignments were made on the basis of the nuclear Overhauser effect (NOE) connectivities of amide protons with preceding amide and/or Cprotons. In addition to sequential NOEs, vicinal spin coupling constants for amide protons and C protons and deuterium exchange rates of amide protons were used to characterize the secondary structure of the GDP-bound Ras protein; six strands and five helices were identified and the topology of these elements was determined. The secondary structure of the Ras protein in solution was mainly consistent with that in crystal as determined by X-ray analyses. The deuterium exchange rates of amide protons were examined to elucidate the dynamic properties of the secondary structure elements of the Ras protein in solution. In solution, the -sheet structure in the Ras protein is rigid, while the second helix (A66-R73) is much more flexible, and the first and fifth helices (S17-124 and V152-L171) are more rigid than other helices. Secondary structure elements at or near the ends of the effector-region loop were found to be much more flexible in solution than in the crystalline state. 相似文献
935.
Paralogous origin of the red- and green-sensitive visual pigment genes in vertebrates 总被引:1,自引:0,他引:1
The nucleotide sequence of the red-sensitive visual pigment gene, R007Af,
in the fish Astyanax fasciatus, from the initiation codon to the stop codon
of this gene, including introns, is 1,592 bp, making it the shortest visual
pigment gene known in vertebrates. Analysis of this and other homologous
sequence data suggests that vertebrates initially had two duplicate genes
and that each ancestor of Astyanax, human, and chicken independently
duplicated the gene in the process of developing their red-green color
vision. Furthermore, many extant red-green colorblind organisms may be
explained simply by the failure of achieving very specific nucleotide
substitutions at the three codon positions 180, 277, and 285, rather than
by the lack of duplicate loci.
相似文献
936.
T. Niimi G. Kawai M. Takayanagi T. Noguchi N. Hayashi T. Kohno Y. Muto K. Watanabe T. Miyazawa S. Yokoyama 《Biochimie》1993,75(12)
Imino 15N and 1H resonances of Escherichia coli tRNAlIle were observed in the absence and presence of E coli isoleucyl-tRNA synthetase. Upon complex formation of tRNAlIle with isoleucyl-tRNA synthetase, some imino 15N-1H resonances disappeared, and some others were significantly broadened and/or shifted in the 1H chemical shift, while the others were observed at the same 15H-1H chemical shifts. It was indicated that the binding of tRNAlIle with IleRS affect the following four regions: the anticodon stem, the junction of the acceptor and T stems, the middle of the D stem, and the region where the tertiary base pair connects the T, D, and extra loops. This result is consistent with those of chemical footprinting and site-directed mutagenesis studies. Taken together, these three independent results reveal the recognition mechanism of tRNAlIle by IleRS: IleRS recognizes all the identity determinants distributed throughout the tRNAlIle molecule, which induces changes in the secondary and tertiary structures of tRNAlIle. 相似文献
937.
The application of 2000 ppm 2-diethylaminoethyl-3,4-dichlorophenylether [DCPTA] to greenhouse-grown Eucommia ulmoides Oliv. plants resulted in an 18% increase in the gutta content. Leaf area and plant height were also enhanced. Field studies employing 100 ppm of a proprietary regulator, FVCL2, produced a 20% increase in leaf gutta.Reference to a company or product name does not imply approval or recommendation of the product by the U.S. Department of Agriculture to the exclusion of others that may be suitable. 相似文献
938.
939.
Mark Ming-Long Hsu MD Jen-Chyi Chang Koji Yokoyama Kazuko Nishimura Makoto Miyaji 《Mycopathologia》1994,127(2):77-81
Twenty-one strains ofCryptococcus neoformans isolated from patients in Taiwan were characterized for serotypes and mating types. Slide agglutination test was performed with 8 factor-specific sera (Iatron Company, Japan) to determine the serotypes. Wheat bran agar (WBA) and malt extract agar (MEA, Wickerham) media were used for the mating tests. Twenty of the isolates were of serotype A, and one was serotype B. Except for 2 strains of serotype A, all of the serotype A strains mated withFilobasidiella neoformans var.neoformans, mating type a. The only serotype B strain mated withF. neoformans var.bacillispora mating type a in MEA medium. These data revealed the low prevalence (1/21; 4.8%) ofC. neoformans var.gattii in Taiwan, a subtropically located island. 相似文献
940.
A novel point mutation (G-1 to T) in a 5' splice donor site of intron 13 of the dystrophin gene results in exon skipping and is responsible for Becker muscular dystrophy. 总被引:3,自引:1,他引:2 下载免费PDF全文
Y. Hagiwara H. Nishio Y. Kitoh Y. Takeshima N. Narita H. Wada M. Yokoyama H. Nakamura M. Matsuo 《American journal of human genetics》1994,54(1):53-61
The mutations in one-third of Duchenne and Becker muscular dystrophy patients remain unknown, as they do not involve gross rearrangements of the dystrophin gene. We now report a defect in the splicing of precursor mRNA (pre-mRNA), resulting from a maternally inherited mutation of the dystrophin gene in a patient with Becker muscular dystrophy. This defect results from a G-to-T transversion at the terminal nucleotide of exon 13, within the 5' splice site of intron 13, and causes complete skipping of exon 13 during processing of dystrophin pre-mRNA. The predicted polypeptide encoded by the aberrant mRNA is a truncated dystrophin lacking 40 amino acids from the amino-proximal end of the rod domain. This is the first report of an intraexon point mutation that completely inactivates a 5' splice donor site in dystrophin pre-mRNA. Analysis of the genomic context of the G-1-to-T mutation at the 5' splice site supports the exon-definition model of pre-mRNA splicing and contributes to the understanding of splice-site selection. 相似文献