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401.
Sheng Yalan Duan Lili Cheng Ting Qiao Yu Stover Naomi A. Gao Shan 《中国科学:生命科学英文版》2020,63(10):1534-1542
The ciliate Tetrahymena thermophila has been a powerful model system for molecular and cellular biology. However, some investigations have been limited due to the incomplete closure and sequencing of the macronuclear genome assembly, which for many years has been stalled at 1,158 scaffolds, with large sections of unknown sequences(available in Tetrahymena Genome Database, TGD, http://ciliate.org/). Here we completed the first chromosome-level Tetrahymena macronuclear genome assembly, with approximately 300× long Single Molecule, Real-Time reads of the wild-type SB210 cells—the reference strain for the initial macronuclear genome sequencing project. All 181 chromosomes were capped with two telomeres and gaps were entirely closed. The completed genome shows significant improvements over the current assembly(TGD 2014) in both chromosome structure and sequence integrity. The majority of previously identified gene models shown in TGD were retained,with the addition of 36 new genes and 883 genes with modified gene models. The new genome and annotation were incorporated into TGD. This new genome allows for pursuit in some underexplored areas that were far more challenging previously; two of them, genome scrambling and chromosomal copy number, were investigated in this study. We expect that the completed macronuclear genome will facilitate many studies in Tetrahymena biology, as well as multiple lines of research in other eukaryotes. 相似文献
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J. Mika B. Przewocka † C. Stover ‡ W. J. Schwaeble ‡ E. Weihe M. K.-H. Schäfer 《Journal of neurochemistry》2003,85(S2):32-32
A number of new synthetic nociceptin ligands were studied in receptor binding and functional tests in rat brain membranes and in cloned systems. Ligand binding experiments were performed with three different radioprobes developed in our lab. The nociceptin derivatives exhibited high affinity in competition experiments. Receptor-mediated G-protein activation was determined in [35 S]GTPgS binding assays. Among the new structures examined, Ac-RYYRIK-ol was found to be only a weak stimulator by itself, whereas this compound inhibited receptor-mediated G-protein activation. These data suggest that Ac-RYYRIK-ol is a high affinity peptide antagonist for the nociceptin receptor.
Acknowledgements: Supported by the Hungarian Scientific Research Fund OTKA T-035211, T-033078, T-030841, and the Ministry of Education, NKFP 1/027 Hungary. 相似文献
Acknowledgements: Supported by the Hungarian Scientific Research Fund OTKA T-035211, T-033078, T-030841, and the Ministry of Education, NKFP 1/027 Hungary. 相似文献
406.
Paul R. De Lay Adle Benzaken Quarraisha Abdool Karim Sani Aliyu Carolyn Amole George Ayala Kalipso Chalkidou Judy Chang Michaela Clayton Aleny Couto Carl Dieffenbach Mark Dybul Wafaa El Sadr Marelize Gorgens Daniel Low-Beer Smail Mesbah Jorge Saveedra Petchsri Sirinirund John Stover Omar Syarif Aditia Taslim Safiatou Thiam Lucy Wanjiku Njenga Peter D. Ghys Jose Antonio Izazola-Licea Luisa Frescura Erik Lamontagne Peter Godfrey-Faussett Christopher Fontaine Iris Semini Shannon Hader 《PLoS medicine》2021,18(6)
Paul De Lay and co-authors introduce a Collection on the design of targets for ending the AIDS epidemic. 相似文献
407.
Lipids were extracted from excised uropygial glands of domestic chickens and the wax diesters were isolated by preparative thin-layer chromatography (TLC). The diesters were hydrolyzed and the liberated diols were resolved by boric acid TLC into two fractions. These were investigated by proton magnetic resonance at 360 MHz of the free diols and of their acetonide derivatives. The results showed that the cis and trans acetonides, formed from the erythro and threo isomers of the diols, respectively, could be distinguished by the degree of magnetic nonequivalence of the two acetonide methyl groups in each molecule. On the presumption that the cis isomer should show the greater nonequivalence of the methyl groups, this configuration was assigned to the acetonides of these diols which had the lesser TLC mobility on boric acid/silica gel. This agrees with the assignment of configuration made by earlier workers on the basis of the relative TLC mobility of the diol isomers on boric acid/silica gel, but was contrary to a previous assignment based on gas-liquid chromatographic (GLC) retention times. We conclude that the erythro isomers of the diols are characterized by lower mobility on boric acid TLC, as well as on silica gel TLC, and form acetonides that have longer retention times on GLC, and greater nonequivalence of the acetonide methyl groups in the NMR spectrum, than do the acetonides of the threo isomers. 相似文献
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