The sequence of a 200 kb portion of a Plasmodium vivax chromosome reveals a high degree of conservation with Plasmodium falciparum chromosome 3

被引:27
作者
Tchavtchitch, M
Fischer, K
Huestis, R
Saul, A
机构
[1] Queensland Inst Med Res, Malaria Biol Lab, Australian Ctr Int Trop Hlth & Nutr, Brisbane, Qld 4029, Australia
[2] Univ Queensland, Brisbane, Qld 4072, Australia
基金
英国惠康基金; 英国医学研究理事会;
关键词
Plasmodium vivax; synteny; chromosome; conservation; homology; sequencing;
D O I
10.1016/S0166-6851(01)00380-2
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Within a 199 866 base pair (bp) portion of a Plasmodium vivax chromosome we identified a conserved linkage group consisting of at least 41 genes homologous to Plasmodium falciparum genes located on chromosome 3. There were no P. vivax homologues of the P. falciparum cytoadherence-linked asexual genes clag 3.2, clag 3.1 and a var C pseudogene found on the P. vivax chromosome. Within the conserved linkage group, the gene order and structure are identical to those of P. falciparum chromosome 3. This conserved linkage group may extend to as many as 190 genes. The subtelomeric regions are different in size and the P. vivax segment contains genes for which no P. falciparum homologues have been identified to date. The size difference of at least 900 kb between the homologous P. vivax chromosome and P. falciparum chromosome 3 is presumably due to a translocation. There is substantial sequence divergence with a much higher guanine + cytosine (G + C) content in the DNA and a preference for amino acids using GC-rich codons in the deduced proteins of P. vivax. This structural conservation of homologous genes and their products combined with sequence divergence at the nucleotide level makes the P. vivax genome a powerful tool for comparative analyses of Plasmodium genomes. (C) 2001 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:211 / 222
页数:12
相关论文
共 38 条
[31]   LONG-RANGE RESTRICTION MAPS OF PLASMODIUM-FALCIPARUM CHROMOSOMES - CROSSING-OVER AND SIZE VARIATION AMONG GEOGRAPHICALLY DISTANT ISOLATES [J].
SINNIS, P ;
WELLEMS, TE .
GENOMICS, 1988, 3 (04) :287-295
[32]  
Stoffel W., 1993, BIOL CHEM HOPPESEYLE, V374, P166, DOI DOI 10.1515/BCHM3.1993.374.1-6.143
[33]  
Tatusova TA, 1999, FEMS MICROBIOL LETT, V174, P247, DOI 10.1016/S0378-1097(99)00149-4
[34]   A PROCEDURE FOR INVITRO AMPLIFICATION OF DNA SEGMENTS THAT LIE OUTSIDE THE BOUNDARIES OF KNOWN SEQUENCES [J].
TRIGLIA, T ;
PETERSON, MG ;
KEMP, DJ .
NUCLEIC ACIDS RESEARCH, 1988, 16 (16) :8186-8186
[35]   RAPID AND EFFICIENT METHOD FOR CLONING OF BLUNT-ENDED DNA FRAGMENTS [J].
UPCROFT, P ;
HEALEY, A .
GENE, 1987, 51 (01) :69-75
[36]   The conserved genome organisation of non-falciparum malaria species: the need to know more [J].
van Lin, LHM ;
Janse, CJ ;
Waters, AP .
INTERNATIONAL JOURNAL FOR PARASITOLOGY, 2000, 30 (04) :357-370
[37]   CHROMOSOME-SIZED DNA-MOLECULES OF PLASMODIUM-FALCIPARUM [J].
VANDERPLOEG, LHT ;
SMITS, M ;
PONNUDURAI, T ;
VERMEULEN, A ;
MEUWISSEN, JHET ;
LANGSLEY, G .
SCIENCE, 1985, 229 (4714) :658-661
[38]   COMPARISON OF INTRONS IN A CDC2-HOMOLOGOUS GENE WITHIN A NUMBER OF PLASMODIUM SPECIES [J].
VINKENOOG, R ;
VELDHUISEN, B ;
SPERANCA, MA ;
DELPORTILLO, HA ;
JANSE, C ;
WATERS, AP .
MOLECULAR AND BIOCHEMICAL PARASITOLOGY, 1995, 71 (02) :233-241