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991.
992.
Maruyama Akiko; Ishizawa Kimiharu; Takagi Takashi; Esashi Yohji 《Plant & cell physiology》1998,39(7):671-680
The activity of rß-cyanoalanine synthase (CAS, EC4.4.1.9
[EC]
) in cotyledons of cocklebur seeds (Xanthium penn-sylvanicumWallr.) was detected both in the soluble and particulate fractions.The CAS activity of the soluble fraction (cytosolic CAS activity)was 10 times higher than that of the particulate fraction. TheCAS activity of the particulate fraction was confirmed to belocalized in the mitochondria. Both enzymatic activities wereclearly separated by non-denaturing PAGE. The enzyme with cytosolicCAS activity has been extensively purified and separated intothree different forms designated as cyt-1, cyt-2, and cyt-3.According to the SDS-PAGE analysis, the three enzymes are estimatedto be a homodimer composed of 35-kDa sub-units. The purifiedenzymes showed CS activity. Partial amino acid sequences ofcyt-1 were determined and had a high homology with cysteinesynthases (CS, EC 4.2.99.8
[EC]
) from other plant sources. The catalyticaction of the purified CSs in converting cyanide and cysteineinto H2S and rß-cyanoalanine was confirmed by thedetection of significant 14CN incorporation into rß-cyanoalanine.These results indicated that cytosolic CAS activity is due tocytosolic CS and suggested that the CAS activity of CS is likelyto be involved in cyanide metabolism in plant tissues. (Received January 7, 1998; Accepted March 16, 1998) 相似文献
993.
994.
Takashi Fujita Hitoshi Hatamoto Mari Miyamoto Taisuke Iwasaki Shin-ichi Takafuji 《Biotechnology letters》1998,20(11):1057-1061
Cell suspensions derived from Acer nikoense callus, not containing (S)-rhododendrol, converted 4-(p-hydroxyphenyl)-2- butanone into (R)-, (S)-rhododendrol and their glycosides. (R)- and (S)-rhododendrol formed was only detected in the culture medium and their glycosides only in the cells. The former compound disappeared within a short time and the latter one also tended to decrease during prolonged culture. Quantitative analysis of rhododendrol glycosides in the callus showed that most of them were (S)-rhododendrol 2-O--D-glucopyranoside and its content was much lower than that of the original plants. © Rapid Science Ltd. 1998 相似文献
995.
A mutation in theCENTRORADIALIS (CEN) gene ofAntirrhinum and in theTERMINAL FLOWER 1 (TFL1) gene ofArabidopsis causes their indeterminate inflorescence to determinate. We clonedCEN/TFL1 homologs fromNicotiana tabacum, the wild-type of which has a determinate inflorescence. TheCEN gene was expressed in the inflorescnece meristem and kept its inflorescence meristem identity, whereas the tobacco homolog
(NCH) was expressed at a low level throughout the plant’s development. AlthoughCEN andNCH are highly homologous genes, they may have been recruited to different developmental functions during their evolution. TwoNCH genes are derived from amphidiploidN. tabacum, but both of them hybridized with its diploid parents,N. sylvestris andN. tomentosiformis. Southern blotting, and the genomic organization ofTFL1 inArabidopsis revealed that anotherCEN homolog exists in the genome ofArabidopsis. These results suggest that there are two copies of theCEN homolog per diploid plant.
The extended abstract of a paper presented at the 13th International Symposium in Conjugation with Award of the International
Prize for Biology “Frontier of Plant Biology”
These two authors contributed to this work equally. 相似文献
996.
Takashi Araki Yasushi Kobayashi Hidetaka Kaya Masaki Iwabuchi 《Journal of plant research》1998,111(2):277-281
Transition from vegetative to reproductive development (flowering) is one of the most important decisions during the post-embryonic
development of flowering plants. More than twenty loci are known to regulate this process inArabidopsis. Some of these flowering-time genes may act at the shoot apical meristem to regulate its competence to respond to floral
inductive signals and floral evocation. Genetic and phenotypic analyses of mutants suggest that the late-flowering geneFT may be a good candidate for such genes. To test this, we have cloned theFT gene using aFT-deficiency line associated with a T-DNA insertion. Cloned genes and loss-of-function mutants in hand, it is now possible
to analyse the role ofFT and other genes in flowering at the biochemical and cellular levels as well as at the genetic level. The deduced FT protein
has homology with TFL1 and CEN proteins believed to be involved in regulation of inflorescence meristem identity. Phylogenetic
analysis suggests that theFT group and theTFL1/CEN group of genes diverged before the diversification of major angiosperm clades. This raises the interesting question of the
evolutionary relationship between the regulation of vegetative/reproductive switching in the shoot apical meristem and the
regulation of inflorescence architecture in angiosperms.
The extended abstract of a paper presented at the 13th International Symposium in Conjugation with Award of the International
Prize for Biology “Fronitier of Plant Biology” 相似文献
997.
Poly(ADP-ribose) glycohydrolase (PARG) digests poly(ADP-ribose), which is synthesized by poly(ADP-ribose) polymerase (PARP) after DNA damage. We mapped the human poly(ADP-ribose) glycohydrolase gene to chromosome 10q11.23-21.1 by fluorescence in situ hybridization analysis. Since chromosomal rearrangements in thyroid papillary carcinoma and loss of heterozygosity in glioblastoma are frequently observed in this region, genetic alteration of PARG could be implicated in these diseases. 相似文献
998.
Yasunori Machida Marina Nakashima Kayoko Morikiyo Hiroharu Banno Masaki Ishikawa Takashi Soyano Ryuichi Nishihama 《Journal of plant research》1998,111(2):243-246
The tobaccoNPK1 gene encodes a homolog of mitogenactivated protein kinase kinase kinases. We have recently identified tobacco kinesin-like
proteins (NACK1/2) as activators for NPK1. Immunochemical analyses of NPK1 and NACK1 proteins suggest that NPK1 is involved
in the regulation of some process in the M phase of the plant cell cycle.
The extended abstract of a paper presented at the 13th International Symposium in Conjugation with Award of the International
Prize for Biology “Frontier of Plant Biology” 相似文献
999.
Yosuke Andoh Takashi Kuramoto Norihide Yokoi Toshiro Maihara Kazuhiro Kitada Tadao Serikawa 《Mammalian genome》1998,9(4):287-293
To correlate rat genetic linkage maps with cytogenetic maps, we localized 25 new cosmid-derived simple sequence length polymorphism
(SSLP) markers and 14 existing genetic markers on cytogenetic bands of chromosomes, using fluorescence in situ hybridization
(FISH). Next, a total of 58 anchor loci, consisting of the 39 new and 19 previously reported ones, were integrated into the
genetic linkage maps. Since most of the new anchor loci were developed to be localized near the terminals of the genetic or
cytogenetic maps for each chromosome, the orientation and coverage of the whole genetic linkage maps were determined or confirmed
with respect to the cytogenetic maps. Thus, we provide here a new base for rat genetic maps.
Received: 9 September 1997 / Accepted: 11 November 1997 相似文献
1000.
Toshikazu Ushijima Tomoko Nomoto Takashi Sugimura David E. Housman Minako Nagao 《Mammalian genome》1998,9(12):1008-1012
Mapping of genetic suppressors, modifiers, and quantitative trait loci (QTLs) requires genetic markers that can be efficiently
and inexpensively genotyped for a large number of individuals. To isolate rat genetic markers suitable for this purpose, representational
difference analysis (RDA) was performed with amplicons prepared by PCR with the B1 repetitive sequence used as the primer
(B1-amplicons). In total, 48 polymorphic DNA fragments were isolated by five series of RDA, subtracting the B1-amplicons prepared
from an ACI/N (ACI) rat from those prepared from BUF/Nac (BUF), and vice versa. All the polymorphic fragments detected ``presence-or-absence'
polymorphisms with B1-amplicons prepared from ACI, BUF, and their F2 progeny, and each fragment was linkage mapped. Dot-blotting amplicons onto filters at a high density and hybridization of
the filters with these B1-RDA markers made it possible to genotype a large number of rats simultaneously for multiple loci.
These B1-RDA markers were polymorphic between two given inbred strains of rat at frequencies between 30% and 70%. This is
the first report on the isolation of B1-RDA markers among inbred strains of rats.
Received: 15 July 1998 / Accepted: 18 August 1998 相似文献