TY - JOUR
T1 - Comparative genome analysis of three eukaryotic parasites with differing abilities to transform leukocytes reveals key mediators of theileria-induced leukocyte transformation
AU - Hayashida, Kyoko
AU - Hara, Yuichiro
AU - Abe, Takashi
AU - Yamasaki, Chisato
AU - Toyoda, Atsushi
AU - Kosuge, Takehide
AU - Suzuki, Yutaka
AU - Sato, Yoshiharu
AU - Kawashima, Shuichi
AU - Katayama, Toshiaki
AU - Wakaguri, Hiroyuki
AU - Inoue, Noboru
AU - Homma, Keiichi
AU - Tada-Umezaki, Masahito
AU - Yagi, Yukio
AU - Fujii, Yasuyuki
AU - Habara, Takuya
AU - Kanehisa, Minoru
AU - Watanabe, Hidemi
AU - Ito, Kimihito
AU - Gojobori, Takashi
AU - Sugawara, Hideaki
AU - Imanishi, Tadashi
AU - Weir, William
AU - Gardner, Malcolm
AU - Pain, Arnab
AU - Shiels, Brian
AU - Hattori, Masahira
AU - Nene, Vishvanath
AU - Sugimoto, Chihiro
N1 - KAUST Repository Item: Exported on 2020-10-01
PY - 2012/9/4
Y1 - 2012/9/4
N2 - We sequenced the genome of Theileria orientalis, a tick-borne apicomplexan protozoan parasite of cattle. The focus of this study was a comparative genome analysis of T. orientalis relative to other highly pathogenic Theileria species, T. parva and T. annulata. T. parva and T. annulata induce transformation of infected cells of lymphocyte or macrophage/monocyte lineages; in contrast, T. orientalis does not induce uncontrolled proliferation of infected leukocytes and multiplies predominantly within infected erythrocytes. While synteny across homologous chromosomes of the three Theileria species was found to be well conserved overall, subtelomeric structures were found to differ substantially, as T. orientalis lacks the large tandemly arrayed subtelomere-encoded variable secreted protein-encoding gene family. Moreover, expansion of particular gene families by gene duplication was found in the genomes of the two transforming Theileria species, most notably, the TashAT/TpHN and Tar/Tpr gene families. Gene families that are present only in T. parva and T. annulata and not in T. orientalis, Babesia bovis, or Plasmo-dium were also identified. Identification of differences between the genome sequences of Theileria species with different abilities to transform and immortalize bovine leukocytes will provide insight into proteins and mechanisms that have evolved to induce and regulate this process. The T. orientalis genome database is available at http://totdb.czc.hokudai.ac.jp/. 2012 Hayashida et al. T.
AB - We sequenced the genome of Theileria orientalis, a tick-borne apicomplexan protozoan parasite of cattle. The focus of this study was a comparative genome analysis of T. orientalis relative to other highly pathogenic Theileria species, T. parva and T. annulata. T. parva and T. annulata induce transformation of infected cells of lymphocyte or macrophage/monocyte lineages; in contrast, T. orientalis does not induce uncontrolled proliferation of infected leukocytes and multiplies predominantly within infected erythrocytes. While synteny across homologous chromosomes of the three Theileria species was found to be well conserved overall, subtelomeric structures were found to differ substantially, as T. orientalis lacks the large tandemly arrayed subtelomere-encoded variable secreted protein-encoding gene family. Moreover, expansion of particular gene families by gene duplication was found in the genomes of the two transforming Theileria species, most notably, the TashAT/TpHN and Tar/Tpr gene families. Gene families that are present only in T. parva and T. annulata and not in T. orientalis, Babesia bovis, or Plasmo-dium were also identified. Identification of differences between the genome sequences of Theileria species with different abilities to transform and immortalize bovine leukocytes will provide insight into proteins and mechanisms that have evolved to induce and regulate this process. The T. orientalis genome database is available at http://totdb.czc.hokudai.ac.jp/. 2012 Hayashida et al. T.
UR - http://hdl.handle.net/10754/325462
UR - https://mbio.asm.org/content/3/5/e00204-12
UR - http://www.scopus.com/inward/record.url?scp=84868378574&partnerID=8YFLogxK
U2 - 10.1128/mBio.00204-12
DO - 10.1128/mBio.00204-12
M3 - Article
C2 - 22951932
SN - 2161-2129
VL - 3
JO - mBio
JF - mBio
IS - 5
ER -