GENOMIC ORGANIZATION OF AN INVARIANT SURFACE GLYCOPROTEIN GENE FAMILY OF TRYPANOSOMA-BRUCEI

被引:17
作者
ZIEGELBAUER, K
RUDENKO, G
KIEFT, R
OVERATH, P
机构
[1] MAX PLANCK INST BIOL,MEMBRANBIOCHEM ABT,D-72076 TUBINGEN,GERMANY
[2] NETHERLANDS CANC INST,DIV MOLEC BIOL,1066 CX AMSTERDAM,NETHERLANDS
关键词
TRYPANOSOMA BRUCEI; INVARIANT SURFACE GLYCOPROTEIN; GENE EXPRESSION; GENOMIC ORGANIZATION;
D O I
10.1016/0166-6851(94)00194-R
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
The genomic organization of a gene family for the invariant surface glycoprotein, ISG75 (invariant surface glycoprotein with a molecular mass of 75 kDa), from Trypanosoma brucei is described. In T. brucei strain 427 ISG75 genes are present in tandem arrays at two loci, A and B, containing 5 and 2 copies, respectively. At the S'-end of locus A, a single gene was identified that encodes a structural isoform of ISG75. This isoform contains a unique amino-terminal domain, whereas the rest of the protein is nearly identical to the polypeptides encoded by the other genes. This isoform is transcribed into a stable mRNA, but the expression of the derived polypeptide was below the detection limit. The ISG75 gene clusters are present on chromosomal bands 9' and 10, supporting the hypothesis of Gottesdiener et al. [25] that these bands contain allelic chromosomes. The total number of ISG75 genes is strain dependent, but at least one copy of the unique isoform is present in every variant tested.
引用
收藏
页码:53 / 63
页数:11
相关论文
共 42 条
  • [21] HUANG J, 1991, EMBO J, V12, P3877
  • [22] A POSSIBLE ROLE FOR THE 3'-UNTRANSLATED REGION IN DEVELOPMENTAL REGULATION IN TRYPANOSOMA-BRUCEI
    HUG, M
    CARRUTHERS, VB
    HARTMANN, C
    SHERMAN, DS
    CROSS, GAM
    CLAYTON, C
    [J]. MOLECULAR AND BIOCHEMICAL PARASITOLOGY, 1993, 61 (01) : 87 - 96
  • [23] TRANSIENT ACTIVITY ASSAYS OF THE TRYPANOSOMA-BRUCEI VARIANT SURFACE GLYCOPROTEIN GENE PROMOTER - CONTROL OF GENE-EXPRESSION AT THE POSTTRANSCRIPTIONAL LEVEL
    JEFFERIES, D
    TEBABI, P
    PAYS, E
    [J]. MOLECULAR AND CELLULAR BIOLOGY, 1991, 11 (01) : 338 - 343
  • [24] KOENIG E, 1989, Nucleic Acids Research, V17, P8727
  • [25] TRANS-SPLICING IN TRYPANOSOMES - ARCHAISM OR ADAPTATION
    LAIRD, PW
    [J]. TRENDS IN GENETICS, 1989, 5 (07) : 204 - 208
  • [26] EVIDENCE FOR GENE CONVERSION BETWEEN THE PHOSPHOGLYCERATE KINASE GENES OF TRYPANOSOMA-BRUCEI
    LEBLANCQ, SM
    SWINKELS, BW
    GIBSON, WC
    BORST, P
    [J]. JOURNAL OF MOLECULAR BIOLOGY, 1988, 200 (03) : 439 - 447
  • [27] A TRANSCRIPTIONAL ANALYSIS OF THE TRYPANOSOMA-BRUCEI HSP83 GENE-CLUSTER
    MOTTRAM, JC
    MURPHY, WJ
    AGABIAN, N
    [J]. MOLECULAR AND BIOCHEMICAL PARASITOLOGY, 1989, 37 (01) : 115 - 128
  • [28] INVARIANT SURFACE-PROTEINS IN BLOOD-STREAM FORMS OF TRYPANOSOMA-BRUCEI
    OVERATH, P
    CHAUDHRI, M
    STEVERDING, D
    ZIEGELBAUER, K
    [J]. PARASITOLOGY TODAY, 1994, 10 (02): : 53 - 58
  • [29] PROCYCLIC ACIDIC REPETITIVE PROTEIN (PARP) GENES LOCATED IN AN UNUSUALLY SMALL ALPHA-AMANITIN-RESISTANT TRANSCRIPTION UNIT - PARP PROMOTER ACTIVITY ASSAYED BY TRANSIENT DNA TRANSFECTION OF TRYPANOSOMA-BRUCEI
    RUDENKO, G
    LEBLANCO, S
    SMITH, J
    LEE, MGS
    RATTRAY, A
    VANDERPLOEG, LHT
    [J]. MOLECULAR AND CELLULAR BIOLOGY, 1990, 10 (07) : 3492 - 3504
  • [30] Sambrook J., 1989, MOL CLONING LAB MANU