Genetic and Epigenetic Mechanisms Underlying Cell-Surface Variability in Protozoa and Fungi

被引:63
作者
Verstrepen, Kevin J. [1 ,2 ]
Fink, Gerald R. [3 ]
机构
[1] VIB, Lab Syst Biol, B-3001 Louvain, Belgium
[2] Katholieke Univ Leuven, Lab Genet & Genom, CMPG, B-3001 Louvain, Belgium
[3] MIT, Whitehead Inst Biomed Res, Cambridge, MA 02142 USA
关键词
phase variation; tandem repeats; satellite repeats; contingency loci; mucin; VAR; VSG; VSG EXPRESSION SITE; MUTUALLY EXCLUSIVE EXPRESSION; ANTIGENIC VARIATION; PLASMODIUM-FALCIPARUM; TRYPANOSOMA-CRUZI; SACCHAROMYCES-CEREVISIAE; TRANS-SIALIDASE; INVASIVE GROWTH; HOMOLOGOUS RECOMBINATION; GENOME SEQUENCE;
D O I
10.1146/annurev-genet-102108-134156
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Eukaryotic microorganisms have evolved ingenious mechanisms to generate variability at their cell surface, permitting differential adherence, rapid adaptation to changing environments, and evasion of immune surveillance. Fungi such as Saccharomyces cerevisiae and the pathogen Candida albicans carry a family Of mucin and adhesin genes that allow adhesion to various Surfaces and tissues. Trypanosoma cruzi, T. brucei, and Plasmodium falciparum likewise contain large arsenals of different cell surface adhesion genes. In both yeasts and protozoa, silencing and differential expression of the gene family results in surface variability. Here, we discuss unexpected similarities in the structure and genomic location of the cell surface genes, the role of repeated DNA sequences, and the genetic and epigenetic mechanisms-all of which contribute to the remarkable cell surface variability in these highly divergent microbes.
引用
收藏
页码:1 / 24
页数:24
相关论文
共 154 条
  • [1] The mucin-like glycoprotein super-family of Trypanosoma cruzi:: structure and biological roles
    Acosta-Serrano, A
    Almeida, IC
    Freitas, LH
    Yoshida, N
    Schenkman, S
    [J]. MOLECULAR AND BIOCHEMICAL PARASITOLOGY, 2001, 114 (02) : 143 - 150
  • [2] Loss of the mono-allelic control of the VSG expression sites during the development of Trypanosoma brucei in the bloodstream
    Amiguet-Vercher, A
    Pérez-Morga, D
    Pays, A
    Poelvoorde, P
    Van Xong, H
    Tebabi, P
    Vanhamme, L
    Pays, E
    [J]. MOLECULAR MICROBIOLOGY, 2004, 51 (06) : 1577 - 1588
  • [3] The Trypanosoma cruzi proteome
    Atwood, JA
    Weatherly, DB
    Minning, TA
    Bundy, B
    Cavola, C
    Opperdoes, FR
    Orlando, R
    Tarleton, RL
    [J]. SCIENCE, 2005, 309 (5733) : 473 - 476
  • [4] MUC1 and the MUCs: A family of human mucins with impact in cancer biology
    Baldus, SE
    Engelmann, K
    Hanisch, FG
    [J]. CRITICAL REVIEWS IN CLINICAL LABORATORY SCIENCES, 2004, 41 (02) : 189 - 231
  • [5] Pathogen escape from host immunity by a genome program for antigenic variation
    Barbour, Alan G.
    Dai, Qiyuan
    Restrepo, Blanca I.
    Stoenner, Herbert G.
    Frank, Steven A.
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2006, 103 (48) : 18290 - 18295
  • [6] Identification of novel activation mechanisms for FLO11 regulation in Saccharomyces cerevisiae
    Barrales, Ramon R.
    Jimenez, Juan
    Ibeas, Jose I.
    [J]. GENETICS, 2008, 178 (01) : 145 - 156
  • [7] The trypanosomiases
    Barrett, MP
    Burchmore, RJS
    Stich, A
    Lazzari, JO
    Frasch, AC
    Cazzulo, JJ
    Krishna, S
    [J]. LANCET, 2003, 362 (9394) : 1469 - 1480
  • [8] VSG gene control and infectivity strategy of metacyclic stage Trypanosoma brucei
    Barry, JD
    Graham, SV
    Fotheringham, M
    Graham, VS
    Kobryn, K
    Wymer, B
    [J]. MOLECULAR AND BIOCHEMICAL PARASITOLOGY, 1998, 91 (01) : 93 - 105
  • [9] Barry JD, 2001, ADV PARASIT, V49, P1, DOI 10.1016/S0065-308X(01)49037-3
  • [10] Identification of a region of PfEMP1 that mediates adherence of Plasmodium falciparum infected erythrocytes to CD36: Conserved function with variant sequence
    Baruch, DI
    Ma, XC
    Singh, HB
    Bi, XH
    Pasloske, BL
    Howard, RJ
    [J]. BLOOD, 1997, 90 (09) : 3766 - 3775