排序方式: 共有11条查询结果,搜索用时 15 毫秒
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C Marchal J Greenblatt B Mendez D Perrin M Hofnung 《Comptes rendus des séances de l'Académie des sciences. Série D, Sciences naturelles》1979,288(1):151-154
The expression of gene lamB, the structural gene for the lambda receptor in E. coli K-12, has been put under the control of the promoter of the lactose operon. This has been done by in vitro recombination using vectors which are derivatives of phage lambda. 相似文献
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A phosphatase complex that dephosphorylates gammaH2AX regulates DNA damage checkpoint recovery 总被引:1,自引:0,他引:1
Keogh MC Kim JA Downey M Fillingham J Chowdhury D Harrison JC Onishi M Datta N Galicia S Emili A Lieberman J Shen X Buratowski S Haber JE Durocher D Greenblatt JF Krogan NJ 《Nature》2006,439(7075):497-501
One of the earliest marks of a double-strand break (DSB) in eukaryotes is serine phosphorylation of the histone variant H2AX at the carboxy-terminal SQE motif to create gammaH2AX-containing nucleosomes. Budding-yeast histone H2A is phosphorylated in a similar manner by the checkpoint kinases Tel1 and Mec1 (ref. 2; orthologous to mammalian ATM and ATR, respectively) over a 50-kilobase region surrounding the DSB. This modification is important for recruiting numerous DSB-recognition and repair factors to the break site, including DNA damage checkpoint proteins, chromatin remodellers and cohesins. Multiple mechanisms for eliminating gammaH2AX as DNA repair completes are possible, including removal by histone exchange followed potentially by degradation, or, alternatively, dephosphorylation. Here we describe a three-protein complex (HTP-C, for histone H2A phosphatase complex) containing the phosphatase Pph3 that regulates the phosphorylation status of gammaH2AX in vivo and efficiently dephosphorylates gammaH2AX in vitro. gammaH2AX is lost from chromatin surrounding a DSB independently of the HTP-C, indicating that the phosphatase targets gammaH2AX after its displacement from DNA. The dephosphorylation of gammaH2AX by the HTP-C is necessary for efficient recovery from the DNA damage checkpoint. 相似文献
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A cDNA encoding RAP74, a general initiation factor for transcription by RNA polymerase II. 总被引:15,自引:0,他引:15
A Finkelstein C F Kostrub J Li D P Chavez B Q Wang S M Fang J Greenblatt Z F Burton 《Nature》1992,355(6359):464-467
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Butland G Peregrín-Alvarez JM Li J Yang W Yang X Canadien V Starostine A Richards D Beattie B Krogan N Davey M Parkinson J Greenblatt J Emili A 《Nature》2005,433(7025):531-537
Proteins often function as components of multi-subunit complexes. Despite its long history as a model organism, no large-scale analysis of protein complexes in Escherichia coli has yet been reported. To this end, we have targeted DNA cassettes into the E. coli chromosome to create carboxy-terminal, affinity-tagged alleles of 1,000 open reading frames (approximately 23% of the genome). A total of 857 proteins, including 198 of the most highly conserved, soluble non-ribosomal proteins essential in at least one bacterial species, were tagged successfully, whereas 648 could be purified to homogeneity and their interacting protein partners identified by mass spectrometry. An interaction network of protein complexes involved in diverse biological processes was uncovered and validated by sequential rounds of tagging and purification. This network includes many new interactions as well as interactions predicted based solely on genomic inference or limited phenotypic data. This study provides insight into the function of previously uncharacterized bacterial proteins and the overall topology of a microbial interaction network, the core components of which are broadly conserved across Prokaryota. 相似文献
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Termination of transcription by nusA gene protein of Escherichia coli 总被引:26,自引:0,他引:26