转录起始位点的英文

• transcription initiation site

• "转录"英文翻译    transcribe; transfer; mixing ...
• "起始"英文翻译    origin; origination; parenta ...
• "位"英文翻译    place; location
• "点"英文翻译    drop
• "转录起始" 英文翻译 :    transcription initiation
• "起始位点" 英文翻译 :    initiation site
• "可变转录起始" 英文翻译 :    alternative transcription initiation
• "转录起始因子" 英文翻译 :    transcription initiation factor
• "转录起始复合体" 英文翻译 :    transcription initiation complex
• "起始位" 英文翻译 :    bit, start; start bit
• "记录起始" 英文翻译 :    record start
• "记录起始标记" 英文翻译 :    start of record mark
• "零位，起始位置" 英文翻译 :    zero position
• "起始位址栏" 英文翻译 :    origin address field，oaf
• "起始位置" 英文翻译 :    datum position; home position; initial position; reference position; starting location
• "传中起始位置" 英文翻译 :    cross from
• "截击起始位置" 英文翻译 :    initial interceptor position
• "零度起始位置" 英文翻译 :    zero starting position
• "起始位置装定" 英文翻译 :    datum setting
• "转录重起始" 英文翻译 :    transcription reinitiation
• "初算位置，起始位置" 英文翻译 :    field position
• "带撇起始位址栏" 英文翻译 :    origin address field prime
• "起始位的下降沿" 英文翻译 :    the falling edge of the start bit
• "起始位置, 复原位置" 英文翻译 :    home position
• "占据发射起始位置" 英文翻译 :    launching organization

• Computational location of transcription start sites in prokaryotic genome based on sliding window
  基于滑动窗口的原核转录起始位点计算定位方法
• By artificially changing a to c at - 137 bp site upstream from transcription start point of cloned promoter , two site - mutation promoters , ipms ( 603 bp ) and ipm1 ( 900 bp ) were created
  通过pcr方法对克隆的两个启动子进行定点突变，使转录起始位点上游- 137bp处a突变为c ，得到两个突变启动子( ipml 、 ipms ) 。
• Activity of each construct was determined . the basal promoter was located at about 60bp up stream of the transcription initiation site . it contains a tata box at - 33bp which is required for the transcription initiation
  基因的基本启动子元件位于转录起始位点上游约60bp ，其中含有一个位于- 33bp处的tatabox ，它对于转录起始起着重要作用。
• 900 bp promoter - directed gus expression was highly induced by sa and bth , while the 603 bp promoter , whether mutated or not , did not respond to sa and bth induction , which indicated that the element in response to sa and bth lied among 575 ~ 872 bp from transcription start site
  全长900bp启动子能够应答sa和bth的诱导，而603bp长的启动子无论突变与否对sa和bth均无应答，证明sa和bth的应答区域在克隆启动子的转录起始位点上游575 872bp之间。
• In order to use the responding ability to the inducers of pr - la promoter , two fragments , ip1 ( 900 bp ) and ips ( 603 bp ) were cloned from tobacco genomic dna by polymerase chain reaction ( pcr ) with primers designed according to the sequence reported in genbank . sequence analysis of the amplified 900 bp fragment indicated that the cloned sequence had 99 % of homology to the known sequence . its transcription start site , tata box and consensus sequence " tgac " conserved in pr genes were identical to those of pr - la promoter
  根据pr - 1a基因的报道序列，设计两对引物，以烟草基因组为模板，通过pcr扩增得到900bp ( ipl )和603bp ( ips )两个目标片段，序列测定表明克隆的启动子与报道序列具有99的同源性，转录起始位点、 tatabox及保守序列tgac与报道序列均完全相同。
• The entire halcs gene is located on a megaplasmid and contains a 849 - bp open reading frame that encodes a polypeptide of 283 amino acids . the promoter is typically haloarchaeal , but the start site of transcription is only seven bases from the 5 ' end of the initiator aug codon , making the halcs transcript another example of a " leadless transcript " in the haloarchaea
  它的一29一24位置上是一“毛幻人” box序列，为典型的嗜盐古菌启动子;它的转录起始位点距离“ atg ”只有7个核普酸，也是典型的嗜盐古菌的“卜adless腼script ’ ’ 。
• It is suggested that 538bp sequence of ast gene 5 " end had been cloned after the 138bp fragment was linked up with the 706bp fragment . the analysis of 538bp sequence with the software of promoter prediction indicated that there maybe exist four transcriptional initiator sites , one caat - box and two gc - boxes
  将该片段与706bp的片段对接后，表明克隆到了ast基因的上游启动子的538bp序列，通过promoterpredict软件进行启动子的分析，显示该序列存在可能的四个转录起始位点，一个caat框和两个gc框。
• In the part i , the sequence of the cloned promoter osg6b " was first analyzed . osg6b " had a whole length of 1688 bp and 98 % homology to known sequence of promoter osg6b . its transcriptional start point , tata boxes and the consensus sequences " tgtgg " conserved usually in anther - specific promoters were identical to those of reported osg6b
  第一部分：对已克隆的启动子osg6b ’进行的序列分析表明， osg6b ’全长1688bp ，与报道的osg6b有98的同源性，两者在转录起始位点、 tatabox及其它花药特异性启动子共有的保守序列tgtgg完全相同。