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Ribosome-binding site

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The optimal distance between the RBS and the start codon is variable - it depends on the portion of the SD sequence encoded in the actual RBS and its distance to the start site of a consensus SD sequence. Optimal spacing increases the rate of translation initiation once a ribosome has been bound. The
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The level of complementarity of the mRNA SD sequence to the ribosomal ASD greatly affects the efficiency of translation initiation. Richer complementarity results in higher initiation efficiency. It is worth noting that this only holds up to a certain point - having too rich of a complementarity is
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Secondary structures formed by the RBS can affect the translational efficiency of mRNA, generally inhibiting translation. These secondary structures are formed by H-bonding of the mRNA base pairs and are sensitive to temperature. At a higher-than-usual temperature (~42 °C), the RBS secondary
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The identification of RBSs is used to determine the site of translation initiation in an unannotated sequence. This is referred to as N-terminal prediction. This is especially useful when multiple start codons are situated around the potential start site of the protein coding sequence.
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Variations of the 5'-AGGAGG-3' sequence have been found in Archaea as highly conserved 5′-GGTG-3′ regions, 5 basepairs upstream of the start site. Additionally, some bacterial initiation regions, such as rpsA in E.coli completely lack identifiable SD sequences.
86:(SD) sequence. The complementary sequence (CCUCCU), called the anti-Shine-Dalgarno (ASD) is contained in the 3’ end of the 16S region of the smaller (30S) ribosomal subunit. Upon encountering the Shine-Dalgarno sequence, the ASD of the ribosome 533:
De Boer, Herman A.; Hui, Anna S. (1990-01-01). " Sequences within ribosome binding site affecting messenger RNA translatability and method to direct ribosomes to single messenger RNA species". In Enzymology, BT - Methods in (ed.).
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Prokaryotic ribosomes begin translation of the mRNA transcript while DNA is still being transcribed. Thus translation and transcription are parallel processes. Bacterial mRNA are usually
202:. This process is not dependent on the full set of translation initiation factors (although this depends on the specific IRES) and is commonly found in the translation of viral mRNA. 128:
The ribosomal protein S1 binds to adenine sequences upstream of the RBS. Increasing the concentration of adenine upstream of the RBS will increase the rate of ribosome recruitment.
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becomes undone thus allowing ribosomes to bind and initiate translation. This mechanism allows a cell to quickly respond to an increase in temperature.
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Identification of RBSs is particularly difficult, because they tend to be highly degenerated. One approach to identifying RBS in E.coli is using
728:"Deriving ribosomal binding site (RBS) statistical models from unannotated DNA sequences and the use of the RBS model for N-terminal prediction" 2031: 2027: 106:
and contain multiple ribosome binding sites. Translation initiation is the most highly regulated step of protein synthesis in prokaryotes.
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G. Since the Kozak sequence itself is not involved in the recruitment of the ribosome, it is not considered a ribosome binding site.
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known to paradoxically decrease the rate of translation as the ribosome then happens to be bound too tightly to proceed downstream.
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Eukaryotic ribosomes are known to bind to transcripts in a mechanism unlike the one involving the 5' cap, at a sequence called the
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composition of nucleotides in the spacer region itself was also found to affect the rate of translation initiation in one study.
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Oliveira, Márcio Ferreira da Silva; Mendes, Daniele Quintella; Ferrari, Luciana Itida; Vasconcelos, Ana Tereza Ribeiro (2004).
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Translation initiation happens following recruitment of the ribosome, at the start codon (underlined) found within the
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the rate at which a recruited ribosome is able to initiate translation (i.e. the translation initiation efficiency)
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Laursen, Brian Søgaard; Sørensen, Hans Peter; Mortensen, Kim Kusk; Sperling-Petersen, Hans Uffe (2005-03-01).
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The RBS in prokaryotes is a region upstream of the start codon. This region of the mRNA has the
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Stormo, Gary D. (2000-01-01). "DNA binding sites: representation and discovery".
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Omotajo, Damilola; Tate, Travis; Cho, Hyuk; Choudhary, Madhusudan (2015-08-14).
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Pisarev, Andrey V.; Shirokikh, Nikolay E.; Hellen, Christopher U.T. (2005).
592: 87: 934: 879: 795: 709: 670: 514: 452: 305:(1975-03-06). "Determinant of cistron specificity in bacterial ribosomes". 960: 618: 561: 1637: 1632: 1627: 334: 51: 1358: 653: 636: 230:
The Shine-Dalgarno sequence, of the prokaryotic RBS, was discovered by
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in 1984 while she was in the Department of Biological Sciences at the
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Stormo, Gary D.; Schneider, Thomas D.; Gold, Larry M. (1982-05-11).
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Noguchi, Hideki; Taniguchi, Takeaki; Itoh, Takehiko (2008-12-01).
66:. Ribosome recruitment in eukaryotes is generally mediated by the 1686: 1661: 1582: 1577: 1572: 1562: 1557: 1512: 1502: 1473: 1463: 1375: 1293: 1281: 1212: 1186: 1176: 1166: 47: 998: 577:"Characterization of translational initiation sites in E. coli" 238:
in 1975. The Kozak consensus sequence was first identified by
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mRNA and recruit the 43S ribosome complex at that location.
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Factors affecting the efficiency of translation initiation
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transcript that is responsible for the recruitment of a
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Hellen, Christopher U. T.; Sarnow, Peter (2001-07-01).
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happens when eukaryote initiation factors elF4F and
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the rate at which a ribosome is recruited to the RBS
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Academic Press. pp. 103–114. 109:The rate of translation depends on two factors: 120:The RBS sequence affects both of these factors. 42:), is a sequence of nucleotides upstream of the 90:with it, after which translation is initiated. 360:"Ribosomal Binding Site Sequence Requirements" 124:Factors affecting rate of ribosome recruitment 1010: 473:"Initiation of Protein Synthesis in Bacteria" 384:"Help:Ribosome Binding Site - parts.igem.org" 8: 726:Hayes, William S.; Borodovsky, Mark (1998). 2191: 1727: 1718: 1535: 1160: 1062: 1053: 1017: 1003: 995: 477:Microbiology and Molecular Biology Reviews 950: 826: 785: 652: 608: 504: 442: 424: 287: 721: 719: 98:Effect on translation initiation rate 7: 630: 628: 528: 526: 524: 466: 464: 462: 354: 352: 293: 291: 194:Internal ribosome entry site (IRES) 256:Alpha operon ribosome binding site 25: 735:Pacific Symposium on Biocomputing 218:. Another approach is using the 828:10.1590/S1415-47572004000400028 864:10.1093/bioinformatics/16.1.16 815:Genetics and Molecular Biology 489:10.1128/MMBR.69.1.101-123.2005 82:5'-AGGAGG-3', also called the 1: 917:Kozak, Marilyn (1984-01-25). 70:present on eukaryotic mRNAs. 60:internal ribosome entry sites 544:10.1016/0076-6879(90)85011-C 200:internal ribosome entry site 2692: 702:10.1016/j.crvi.2005.02.004 536:Gene Expression Technology 2621:Aminoacyl tRNA synthetase 426:10.1186/s12864-015-1808-6 54:during the initiation of 2645:Kozak consensus sequence 690:Comptes Rendus Biologies 244:University of Pittsburgh 184:Kozak consensus sequence 167:Ribosome recruitment in 2641:Shine-Dalgarno sequence 641:Genes & Development 173:poly(A)-binding protein 27:Sequence of nucleotides 923:Nucleic Acids Research 581:Nucleic Acids Research 261:Eukaryotic translation 36:ribosomal binding site 18:Ribosomal binding site 770:10.1093/dnares/dsn027 593:10.1093/nar/10.9.2971 266:Bacterial translation 175:(PABP) recognize the 32:ribosome binding site 2666:Protein biosynthesis 1541:​Mitochondrial 1026:Protein biosynthesis 935:10.1093/nar/12.2.857 364:www.thermofisher.com 271:Archaeal translation 319:1975Natur.254...34S 152:heat shock proteins 145:Heat shock proteins 1714:Ribosomal Proteins 654:10.1101/gad.891101 162: 2671:Molecular biology 2653: 2652: 2609: 2608: 2605: 2604: 2601: 2600: 2181: 2180: 1670: 1669: 1594:​Eukaryotic 1531:Elongation factor 1525: 1524: 1521: 1520: 1058:Initiation factor 898:www.garvan.org.au 647:(13): 1593–1612. 16:(Redirected from 2683: 2192: 1728: 1719: 1593: 1540: 1536: 1506: 1467: 1379: 1297: 1216: 1170: 1161: 1063: 1054: 1019: 1012: 1005: 996: 989: 988: 986: 985: 971: 965: 964: 954: 914: 908: 907: 905: 904: 890: 884: 883: 847: 841: 840: 830: 806: 800: 799: 789: 749: 743: 742: 732: 723: 714: 713: 681: 675: 674: 656: 632: 623: 622: 612: 587:(9): 2971–2996. 572: 566: 565: 530: 519: 518: 508: 468: 457: 456: 446: 428: 404: 398: 397: 395: 394: 380: 374: 373: 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Retrieved 978: 969: 926: 922: 912: 901:. Retrieved 897: 888: 858:(1): 16–23. 855: 851: 845: 818: 814: 804: 761: 758:DNA Research 757: 747: 738: 734: 693: 689: 679: 644: 640: 584: 580: 570: 535: 480: 476: 416: 413:BMC Genomics 412: 402: 391:. Retrieved 387: 378: 367:. Retrieved 363: 310: 306: 303:Dalgarno, L. 229: 213: 209: 197: 187: 181: 166: 148: 139: 135: 127: 119: 108: 101: 92: 77: 39: 35: 31: 29: 2631:Start codon 2416:28S subunit 2195:39S subunit 1995:40S subunit 1732:60S subunit 1723:Cytoplasmic 1187:SUI1 family 1030:translation 74:Prokaryotes 56:translation 44:start codon 2660:Categories 2636:Stop codon 1980:RRP15-like 1790:RPL10-like 1539:Bacterial/ 1156:Eukaryotic 1042:eukaryotic 984:2015-11-10 903:2015-11-10 741:: 279–290. 419:(1): 604. 393:2015-10-16 369:2015-10-16 282:References 232:John Shine 169:eukaryotes 158:Eukaryotes 88:base pairs 64:eukaryotes 1592:Archaeal/ 1067:Bacterial 1034:bacterial 943:0305-1048 872:1367-4803 837:1415-4757 778:1340-2838 663:0890-9369 601:0305-1048 497:1092-2172 435:1471-2164 299:Shine, J. 177:5' capped 80:consensus 1683:Class 1 1123:Archaeal 1050:Proteins 1038:archaeal 880:10812473 796:18940874 710:15992743 671:11445534 515:15755955 453:26268350 250:See also 222:method. 52:ribosome 1985:RSL24D1 1662:a/eEF-2 1601:a/eEF-1 961:6694911 787:2608843 619:7048258 562:2199771 506:1082788 444:4535381 343:4162567 315:Bibcode 226:History 2153:RPS27A 2093:RPS15A 2032:RPS4Y2 2028:RPS4Y1 2022:RPS4 ( 1940:RPL37A 1930:RPL36A 1920:RPL35A 1880:RPL27A 1860:RPL23A 1835:RPL18A 1810:RPL13A 1785:RPL10A 1240:γ 1235:β 1228:kinase 1223:α 959:  952:318541 949:  941:  878:  870:  835:  794:  784:  776:  708:  669:  661:  617:  610:320669 607:  599:  560:  550:  513:  503:  495:  451:  441:  433:  341:  335:803646 333:  307:Nature 163:5' cap 68:5' cap 46:of an 2423:MRPS1 2202:MRPL1 2173:RACK1 2168:RPS30 2163:RPS29 2158:RPS28 2148:RPS27 2143:RPS26 2138:RPS25 2133:RPS24 2128:RPS23 2123:RPS21 2118:RPS20 2113:RPS19 2108:RPS18 2103:RPS17 2098:RPS16 2088:RPS15 2083:RPS14 2078:RPS13 2073:RPS12 2068:RPS11 2063:RPS10 2024:RPS4X 2018:RPS3A 1975:RPLP2 1970:RPLP1 1965:RPLP0 1960:RPL41 1955:RPL40 1950:RPL39 1945:RPL38 1935:RPL37 1925:RPL36 1915:RPL35 1910:RPL34 1905:RPL32 1900:RPL31 1895:RPL30 1890:RPL29 1885:RPL28 1875:RPL27 1870:RPL26 1865:RPL24 1855:RPL23 1850:RPL22 1845:RPL21 1840:RPL19 1830:RPL18 1825:RPL17 1820:RPL15 1815:RPL14 1805:RPL13 1800:RPL12 1795:RPL11 1780:RPL10 1765:RPL7A 1702:GSPT2 1697:GSPT1 1553:EF-Ts 1548:EF-Tu 1479:EIF5A 1282:eIF2D 1250:eIF2B 1245:eIF2A 1194:eIF1A 1113:MTIF3 1108:MTIF2 1103:MTIF1 731:(PDF) 339:S2CID 34:, or 2058:RPS9 2053:RPS8 2048:RPS7 2043:RPS6 2038:RPS5 2013:RPS3 2008:RPS2 2003:RPSA 1775:RPL9 1770:RPL8 1760:RPL7 1755:RPL6 1750:RPL5 1745:RPL4 1740:RPL3 1687:eRF1 1583:GFM2 1578:GFM1 1573:TSFM 1568:EF-P 1563:EF-4 1558:EF-G 1513:EIF6 1503:eIF6 1474:EIF5 1464:eIF5 1376:eIF4 1294:eIF3 1213:eIF2 1177:eIF1 1167:eIF1 1146:aIF6 1141:aIF5 1136:aIF2 1131:aIF1 957:PMID 939:ISSN 876:PMID 868:ISSN 833:ISSN 792:PMID 774:ISSN 706:PMID 667:PMID 659:ISSN 615:PMID 597:ISSN 558:PMID 548:ISBN 511:PMID 493:ISSN 449:PMID 431:ISSN 331:PMID 234:and 48:mRNA 1085:IF3 1080:IF2 1075:IF1 947:PMC 931:doi 860:doi 823:doi 782:PMC 766:doi 698:doi 694:328 649:doi 605:PMC 589:doi 540:doi 501:PMC 485:doi 439:PMC 421:doi 323:doi 311:254 188:AUG 186:ACC 40:RBS 2662:: 2593:35 2588:34 2583:33 2578:32 2573:31 2568:30 2563:29 2558:28 2553:27 2548:26 2543:25 2538:24 2533:23 2528:22 2523:21 2518:20 2513:19 2508:18 2503:17 2498:16 2493:15 2488:14 2483:13 2478:12 2473:11 2468:10 2407:42 2402:41 2397:40 2392:39 2387:38 2382:37 2377:36 2372:35 2367:34 2362:33 2357:32 2352:31 2347:30 2342:29 2337:28 2332:27 2327:26 2322:25 2317:24 2312:23 2307:22 2302:21 2297:20 2292:19 2287:18 2282:17 2277:16 2272:15 2267:14 2262:13 2257:12 2252:11 2247:10 2030:, 2026:, 1638:P3 1633:P2 1628:P1 1606:A1 1491:5B 1408:E1 1040:, 1036:, 1028:: 977:. 955:. 945:. 937:. 927:12 925:. 921:. 896:. 874:. 866:. 856:16 854:. 831:. 819:27 817:. 813:. 790:. 780:. 772:. 762:15 760:. 756:. 737:. 733:. 718:^ 704:. 692:. 688:. 665:. 657:. 645:15 643:. 639:. 627:^ 613:. 603:. 595:. 585:10 583:. 579:. 556:. 546:. 523:^ 509:. 499:. 491:. 481:69 479:. 475:. 461:^ 447:. 437:. 429:. 417:16 415:. 411:. 386:. 362:. 351:^ 337:. 329:. 321:. 309:. 301:; 290:^ 246:. 30:A 2643:/ 2463:9 2458:8 2453:7 2448:6 2443:5 2438:4 2433:3 2428:2 2242:9 2237:8 2232:7 2227:6 2222:5 2217:4 2212:3 2207:2 2034:) 1655:G 1650:E 1645:D 1623:B 1616:3 1611:2 1484:2 1452:H 1447:B 1440:3 1435:2 1430:1 1425:G 1418:3 1413:2 1401:3 1396:2 1391:1 1386:A 1364:M 1359:L 1354:K 1349:J 1344:I 1339:H 1334:G 1329:F 1324:E 1319:D 1314:C 1309:B 1304:A 1275:5 1270:4 1265:3 1260:2 1255:1 1199:Y 1182:B 1044:) 1032:( 1018:e 1011:t 1004:v 987:. 963:. 933:: 906:. 882:. 862:: 839:. 825:: 798:. 768:: 739:3 712:. 700:: 673:. 651:: 621:. 591:: 564:. 542:: 517:. 487:: 455:. 423:: 396:. 372:. 345:. 325:: 317:: 38:( 20:)

Index

Ribosomal binding site
start codon
mRNA
ribosome
translation
internal ribosome entry sites
eukaryotes
5' cap
consensus
Shine-Dalgarno
base pairs
polycistronic
heat shock proteins
eukaryotes
poly(A)-binding protein
5' capped
Kozak consensus sequence
internal ribosome entry site
neural networks
Gibbs sampling
John Shine
Lynn Dalgarno
Marilyn Kozak
University of Pittsburgh
Alpha operon ribosome binding site
Eukaryotic translation
Bacterial translation
Archaeal translation
Gene prediction

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