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991.
992.
The gerreid species,Gerres baconensis (Evermann &; Seale),G. equulus Temminck &; Schlegel andG. oyena (Forsskål), were re-assessed as valid following examination of their holotypes and other specimens, and included in the “G. oyena complex”.Gerres haconensis is currently known only from Bacon, Luzon Island, Philippines and the Ogasawara (=Bonin) Islands, Japan, andG. equulus only from southern Japan (except Ryukyu Islands) and southern Korea.Gerres oyena is widely distributed in the Indo-West Pacific (in Japan, only from the Ryukyu Islands).Gerres baconensis differs from bothG. equulus andG. oyena in having higher counts of both the pored lateral line scales (39–42 vs 35–41 in the latter two species) and the lower gill raker series (8 or 9 vs. usually 7). A U-shaped premaxillary groove, formed on the dorsum of the forehead by the long ascending processes of the premaxillae, is scaleless inG. equulus andG. oyena, whereas it is fully scaled just behind the level of the posterior nostrils inG. baconensis over ca. 160 mm in standard length (SL) (partially scaled in specimens of ca. 100 mm SL).Gerres equulus differs fromG. oyena in having the posterior margin of the maxilla not extending beyond a vertical through the anterior margin of the inner dermal eye opening, shorter second dorsal and anal fin spines (means 18.5% and 8.5% of SL, respectively vs. 21.2% and 10.3% of SL), lower body depth at first anal fin spine base (27.0% vs. 29.6% of SL) and dorsomedial U-shaped groove scaleles throughout life (vs. tiny squamation anteriorly in specimens over ca. 130 mm SL). OtherGerres species of uncertain status and/or related species are discussed. 相似文献
993.
M Matsumoto N Tanaka H Harada T Kimura T Yokochi M Kitagawa C Schindler T Taniguchi 《Biological chemistry》1999,380(6):699-703
994.
C S Watson S E White J H Homan K A Kimura J F Brien L Fraher J R Challis A D Bocking 《Journal of applied physiology》1999,86(4):1410-1420
Adenosine and PGE2 are neuromodulators, both of which inhibit fetal breathing movements (FBM). Although circulating PGE2 has been implicated as a mediator of ethanol-induced inhibition of FBM in the late-gestation ovine fetus, a role for adenosine has not been examined. The objective of this study was to determine the effect of maternal ethanol infusion on ovine fetal cerebral extracellular fluid adenosine and PGE2 concentrations by using in utero microdialysis and to relate any changes to ethanol-induced inhibition of FBM. Dialysate samples were obtained from the fetal parietal cortex over 70 h after surgery to determine steady-state extracellular fluid adenosine and PGE2 concentrations. On each of postoperative days 3 and 4, after a 2-h baseline period, ewes received a 1-h infusion of ethanol (1 g/kg maternal body wt) or an equivalent volume of saline, and the fetus was monitored for a further 11 h with 30-min dialysate samples collected throughout. Immediately after surgery, dialysate PGE2 and adenosine concentrations were 3.7 +/- 0.7 and 296 +/- 127 nM, respectively. PGE2 did not change over the 70 h, whereas adenosine decreased to 59 +/- 14 nM (P < 0.05) at 4 h and then remained unchanged. Ethanol decreased dialysate PGE2 concentration for 2 h (3.3 +/- 0.3 to 1.9 +/- 0.4 nM; P < 0.05) and increased adenosine concentration for 6 h (87 +/- 13 to a maximum of 252 +/- 59 nM, P < 0.05). Ethanol decreased FBM incidence from 47 +/- 7 to 16 +/- 5% (P < 0.01) for 8 h. Saline infusion did not change dialysate adenosine or PGE2 concentrations or FBM incidence. These data are consistent with the hypothesis that fetal cerebral adenosine, and not PGE2, is the primary mediator of ethanol-induced inhibition of FBM at 123 days of gestation in sheep. 相似文献
995.
996.
S Asano T Kimura S Ueno M Kawamura N Takeguchi 《The Journal of biological chemistry》1999,274(32):22257-22265
Gastric H(+),K(+)-ATPase consists of alpha-subunit with 10 transmembrane domains and beta-subunit with a single transmembrane domain. We constructed cDNAs encoding chimeric beta-subunits between the gastric H(+),K(+)-ATPase and Na(+),K(+)-ATPase beta-subunits and co-transfected them with the H(+),K(+)-ATPase alpha-subunit cDNA in HEK-293 cells. A chimeric beta-subunit that consists of the cytoplasmic plus transmembrane domains of Na(+),K(+)-ATPase beta-subunit and the ectodomain of H(+),K(+)-ATPase beta-subunit assembled with the H(+),K(+)-ATPase alpha-subunit and expressed the K(+)-ATPase activity. Therefore, the whole cytoplasmic and transmembrane domains of H(+),K(+)-ATPase beta-subunit were replaced by those of Na(+),K(+)-ATPase beta-subunit without losing the enzyme activity. However, most parts of the ectodomain of H(+),K(+)-ATPase beta-subunit were not replaced by the corresponding domains of Na(+), K(+)-ATPase beta-subunit. Interestingly, the extracellular segment between Cys(152) and Cys(178), which contains the second disulfide bond, was exchangeable between H(+),K(+)-ATPase and Na(+), K(+)-ATPase, preserving the K(+)-ATPase activity intact. Furthermore, the K(+)-ATPase activity was preserved when the N-terminal first 4 amino acids ((67)DPYT(70)) in the ectodomain of H(+),K(+)-ATPase beta-subunit were replaced by the corresponding amino acids ((63)SDFE(66)) of Na(+),K(+)-ATPase beta-subunit. The ATPase activity was abolished, however, when 4 amino acids ((76)QLKS(79)) in the ectodomain of H(+),K(+)-ATPase beta-subunit were replaced by the counterpart ((72)RVAP(75)) of Na(+),K(+)-ATPase beta-subunit, indicating that this region is the most N-terminal one that discriminates the H(+),K(+)-ATPase beta-subunit from that of Na(+), K(+)-ATPase. 相似文献
997.
K Eto S Suga M Wakui Y Tsubamoto Y Terauchi J Taka S Aizawa M Noda S Kimura H Kasai T Kadowaki 《The Journal of biological chemistry》1999,274(36):25386-25392
The NADH shuttle system is composed of the glycerol phosphate and malate-aspartate shuttles. We generated mice that lack mitochondrial glycerol-3-phosphate dehydrogenase (mGPDH), a rate-limiting enzyme of the glycerol phosphate shuttle. Application of aminooxyacetate, an inhibitor of the malate-aspartate shuttle, to mGPDH-deficient islets demonstrated that the NADH shuttle system was essential for coupling glycolysis with activation of mitochondrial ATP generation to trigger glucose-induced insulin secretion. The present study revealed that blocking the NADH shuttle system severely suppressed closure of the ATP-sensitive potassium (K(ATP)) channel and depolarization of the plasma membrane in response to glucose in beta cells, although properties of the K(ATP) channel on the excised beta cell membrane were unaffected. In mGPDH-deficient islets treated with aminooxyacetate, Ca(2+) influx through the plasma membrane induced by a depolarizing concentration of KCl in the presence of the K(ATP) channel opener diazoxide restored insulin secretion. However, the level of the secretion was only approximately 40% of wild-type controls. Thus, glucose metabolism through the NADH shuttle system leading to efficient ATP generation is pivotal to activation of both the K(ATP) channel-dependent pathway and steps distal to an elevation of cytosolic Ca(2+) concentration in glucose-induced insulin secretion. 相似文献
998.
Taku Fujiwara Yutaka Terao Tomonori Hoshino Shigetada Kawabata Takashi Ooshima Shizuo Sobue Shigenobu Kimura Shigeyuki Hamada 《FEMS microbiology letters》1998,161(2):331-336
Three glucosyltransferase (GTase) genes (gtfB, gtfC and gtfD) were cloned and sequenced from clinically isolated strains of Streptococcus mutans MT8148 (serotype c), MT4239 (c), MT4245 (e), MT4467 (e) and MT4251 (f), respectively. Comparison of the gtf genes revealed that interstrain difference of gtfB and gtfD was limited, while gtfC showed significant interstrain variations. Similar to gtfB and gtfD, gtfC possessed five direct repeats composed of homologous unit in the carboxyl-terminal portion. The repeating unit consisted of 63–65 amino acid residues and is responsible for glucan binding. The gtfC gene from S. mutans MT4245 lacked the fourth unit. Multiple alignment with the gtf sequence of strain GS-5 (c) revealed several changes in these gtf genes due to frameshift mutations. The peptides encoded by the gtfB, gtfC and gtfD genes of GS-5 were 1, 80, and 32 amino acid residues shorter than those of the test strains except strain MT4245. 相似文献
999.
M. Kato Toshiyuki Kimura Changqing Lin Aiko Ito Soichi Kodama Tateki Morikawa Takashi Soga Kiyoshi Hayasaka 《Human genetics》1999,104(4):341-344
The doublecortin (DCX) gene was recently found to be involved in patients with X-linked lissencephaly and subcortical band
heterotopia or double cortex syndrome. We have studied the coding regions of the DCX gene in 11 Japanese patients with cortical
dysplasia and have identified three different mutations (R186C in exon 3, R272X and R303X in exon 5) in four sporadic female
cases. R272X, which has been detected in two unrelated cases, is a novel mutation. Although the number of cases studied remains
limited, exon 5 may be a common mutational site in Japanese patients in contrast to many previus reports concerning exons
2 and 3.
Received: 28 October 1998 / Accepted: 26 February 1999 相似文献
1000.
T Shibasaki K Moroi M Nishiyama J Zhou A Sakamoto T Masaki K Ito T Haga S Kimura 《Biochemistry and molecular biology international》1999,47(4):569-577
The role of phosphorylation of the C-terminal tail of endothelin B receptor (ETBR) in agonist-induced desensitization was investigated, using a mutant lacking C-terminal 40 amino acids (delta 40 ETBR). In cells expressing the wild type or delta 40 ETBR, ET-1 caused rapid desensitization of calcium responses. The wild type ETBR was phosphorylated by biotinylated ET-1, and the phosphorylation was markedly enhanced by coexpression with G protein-coupled receptor kinase 2 (GRK2). However, delta 40 ETBR was not phosphorylated regardless of coexpression with GRK2. On the other hand, ET-1-induced IP3 formation in these cells was decreased by coexpression with GRK2 or catalytically inactive Lys220Arg GRK2 to the similar extent. The present study demonstrates the presence of phosphorylation-independent desensitization mechanism in delta 40 ETBR and suggests that GRK2 might play a role other than that as a kinase. 相似文献