Stem Trace: An interactive visual tool for comparative RNA structure analysis

被引:21
作者
Kasprzak, W
Shapiro, BA
机构
[1] NCI, Frederick Canc Res & Dev Ctr, SAIC Frederick, Intramur Res Supp Progr,NIH, Frederick, MD 21702 USA
[2] NCI, Frederick Canc Res & Dev Ctr, Image Proc Sect, Lab Expt & Computat Biol,Div Basic Sci,NIH, Frederick, MD 21702 USA
关键词
D O I
10.1093/bioinformatics/15.1.16
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Motivation: Stem Trace is one of the latest tools available in STRUCTURELAB, an RNA structure analysis computer workbench. The paradigm used in STRUCTURELAB views RNA structure determination as a problem of dealing with a database of a large number of computationally generated structures. Stem Trace provides the capability to analyse this data set in a novel, visually driven, interactive and exploratory way In addition to providing graphs at a high level of abstraction, it is also connected with complementary visualization tools which provide orthogonal views of the same data, as well as drawing of structures represented by a stem trace. Thus, on top of being an analysis tool, Stem Trace is a graphical user interface to an RNA structural information database. Results: We illustrate Stem Trace's capabilities with several examples of the analysis of RNA folding data performed rf on 24 strains of HIV-1, HIV-2 and SIV sequences around the HIV dimerization region. This dimer linkage site has been found to play a role in encapsidation, reverse transcription, recombination, and inhibition of translation. Our examples show how Stern Trace elucidates preservation of structures in this region across the various strains of HIV. Availability: The program can be made available upon request. It runs on SUN; SGI and DEC (Compaq) Unix workstations.
引用
收藏
页码:16 / 31
页数:16
相关论文
共 32 条
[1]  
BAUDIN F, 1993, J MOL BIOL, V229, P379
[2]   Requirements for kissing-loop-mediated dimerization of human immunodeficiency virus RNA [J].
Clever, JL ;
Wong, ML ;
Parslow, TG .
JOURNAL OF VIROLOGY, 1996, 70 (09) :5902-5908
[3]  
Currey KM, 1997, COMPUT APPL BIOSCI, V13, P1
[4]   CIS ELEMENTS AND TRANS-ACTING FACTORS INVOLVED IN THE RNA DIMERIZATION OF THE HUMAN-IMMUNODEFICIENCY-VIRUS HIV-1 [J].
DARLIX, JL ;
GABUS, C ;
NUGEYRE, MT ;
CLAVEL, F ;
BARRESINOUSSI, F .
JOURNAL OF MOLECULAR BIOLOGY, 1990, 216 (03) :689-699
[5]   IMPROVED FREE-ENERGY PARAMETERS FOR PREDICTIONS OF RNA DUPLEX STABILITY [J].
FREIER, SM ;
KIERZEK, R ;
JAEGER, JA ;
SUGIMOTO, N ;
CARUTHERS, MH ;
NEILSON, T ;
TURNER, DH .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1986, 83 (24) :9373-9377
[6]   Finding the most significant common sequence and structure motifs in a set of RNA sequences [J].
Gorodkin, J ;
Heyer, LJ ;
Stormo, GD .
NUCLEIC ACIDS RESEARCH, 1997, 25 (18) :3724-3732
[7]  
GROENIK M, 1995, J VIROL, V65, P1968
[8]   Completion of nucleotide sequences of non-syncytium-inducing and syncytium-inducing HIV type 1 variants isolated from the same patient [J].
Guillon, C ;
Bedin, F ;
Fouchier, RAM ;
Schuitemaker, H ;
Gruters, RA .
AIDS RESEARCH AND HUMAN RETROVIRUSES, 1995, 11 (12) :1537-1538
[9]   Evidence that a kissing loop structure facilitates genomic RNA dimerisation in HIV-1 [J].
Haddrick, M ;
Lear, AL ;
Cann, AJ ;
Heaphy, S .
JOURNAL OF MOLECULAR BIOLOGY, 1996, 259 (01) :58-68
[10]   Ultrastructure of HIV-1 genomic RNA [J].
Hoglund, S ;
Ohagen, A ;
Goncalves, J ;
Panganiban, AT ;
Gabuzda, D .
VIROLOGY, 1997, 233 (02) :271-279