轉錄起始位點 的英文怎麼說

中文拼音 [zhuǎnlùqǐshǐwèidiǎn]
轉錄起始位點 英文
transcription initiation site
  • 轉 : 轉構詞成分。
  • 錄 : Ⅰ名1 （用做記載物的名稱） record; register; collection; selections 2 （姓氏） a surname Ⅱ動詞1 （...
  • 起 : 起Ⅰ動詞1 （站起; 坐起） rise; get up; stand up 2 （取出; 取走） draw out; remove; extract; pull 3...
  • 始 : Ⅰ名詞1 （最初; 起頭） beginning; start 2 （姓氏） a surname Ⅱ動詞（開始） start; begin Ⅲ副詞[書面...
  • 位 : Ⅰ名詞1 （所在或所佔的地方） place; location 2 （職位; 地位） position; post; status 3 （特指皇帝...
  • 點 : Ⅰ名詞1 （液體的小滴） drop （of liquid） 2 （細小的痕跡） spot; dot; speck 3 （漢字的筆畫「、」）...
  • 轉錄 : [電學] transcribe; transfer; [聲學] mixing; rerecording; [生物學] transcription; duplicating轉錄...
  • 起始 : origin; origination; parentage; germ; initiation
  1. 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，為典型的嗜鹽古菌啟動子;它的轉錄起始位點距離「 atg 」只有7個核普酸，也是典型的嗜鹽古菌的「卜adless靦script 』 』 。
  2. Computational location of transcription start sites in prokaryotic genome based on sliding window

    基於滑動窗口的原核轉錄起始位點計算定位方法
  3. 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

    通過pcr方法對克隆的兩個啟動子進行定點突變，使轉錄起始位點上游- 137bp處a突變為c ，得到兩個突變啟動子（ ipml 、 ipms ） 。
  4. 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

    基因的基本啟動子元件位於轉錄起始位點上游約60bp ，其中含有一個位於- 33bp處的tatabox ，它對于轉錄起始起著重要作用。
  5. 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

    全長900bp啟動子能夠應答sa和bth的誘導，而603bp長的啟動子無論突變與否對sa和bth均無應答，證明sa和bth的應答區域在克隆啟動子的轉錄起始位點上游575 872bp之間。
  6. 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

    根據pr - 1a基因的報道序列，設計兩對引物，以煙草基因組為模板，通過pcr擴增得到900bp （ ipl ）和603bp （ ips ）兩個目標片段，序列測定表明克隆的啟動子與報道序列具有99的同源性，轉錄起始位點、 tatabox及保守序列tgac與報道序列均完全相同。
  7. 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

    將該片段與706bp的片段對接后，表明克隆到了ast基因的上游啟動子的538bp序列，通過promoterpredict軟體進行啟動子的分析，顯示該序列存在可能的四個轉錄起始位點，一個caat框和兩個gc框。
  8. 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：對已克隆的啟動子osg6b 』進行的序列分析表明， osg6b 』全長1688bp ，與報道的osg6b有98的同源性，兩者在轉錄起始位點、 tatabox及其它花藥特異性啟動子共有的保守序列tgtgg完全相同。
  9. Using transfac 4. 0 and tssg tssh nsite of softbeny, we can see that a tata box lie in - 188bp - 198bp from transcriptional initiation site, there are several api, c / ebp binding motifs near it or in other 5 " flanking region, a c - fos response element is in - 1133bp - 1143bp from transcriptional initiation site

    0軟體和softbeny網站上tssg ， tssh ， nsi 』 fe軟體共同分析，在a ? ibgp轉錄起始點上游j到一198區域存在tata盒，在其附近及其5 』上游遠端調節區存在多個api ， c ebp結合位點，並且在轉錄起始點上遊人到一處存在一個c fos結合基序。
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