Expression profiling the human septin gene family

被引:148
作者
Hall, PA
Jung, K
Hillan, KJ
Russell, SEH
机构
[1] Queens Univ Belfast, Belfast City Hosp, Ctr Canc Res & Cell Biol, Belfast BT9 7AB, Antrim, North Ireland
[2] Genentech Inc, San Francisco, CA 94080 USA
关键词
septin; phylogeny; expression profile; microarray; lymphoid; CNS;
D O I
10.1002/path.1789
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The septins are an evolutionarily conserved family of GTP-binding proteins involved in diverse processes including vesicle trafficking, apoptosis, remodelling of the cytoskeleton, infection, neurodegeneration, and neoplasia. The present paper reports a comprehensive study of septin gene expression by DNA microarray methods in 10360 samples of normal, diseased, and tumour tissues. A novel septin, SEPT13, has been identified and is shown to be related to SEPT7. It is shown that SEPT13 and the other known human septins are expressed in all tissue types but some show high expression in lymphoid (SEPT], 6, 9, and 12) or brain tissues (SEPT2, 3, 4, 5, 7, 8, and 11). For a given septin, some isoforms are highly expressed in the brain and others are not. For example, SEPT8_v2 and v3, 1* and 3 are highly expressed in the brain and cluster with SEPT2, 3, 4, 5, 7, and 11 However, a probe set specific for SEPT8_v1 with low brain expression clusters away from this set. Similarly, SEPT4 has lymphoid and non-lymphoid forms; SEPT2 has lymphoid and central nervous system (CNS) forms; and SEPT6 and SEPT9 are elevated in lymphoid tissues but both have forms that cluster away from the lymphoid forms. Perturbation of septin expression was widespread in disease and tumours of the various tissues examined, particularly for conditions of the CNS, where alterations in all 13 septin genes were identified. This analysis provides a comprehensive catalogue of the septin family in health and disease. It is a key step in understanding the role of septins in physiological and pathological states and provides insight into the complexity of septin biology. Copyrigbt (c) 2005 Pathological Society of Great Britain and Ireland. Published by John Wiley & Sons, Ltd.
引用
收藏
页码:269 / 278
页数:10
相关论文
共 51 条
  • [1] Cancer - New-age tumour suppressors
    Balmain, A
    [J]. NATURE, 2002, 417 (6886) : 235 - 237
  • [2] Isolation of new splice isoforms, characterization and expression analysis of the human septin SEPT8 (KIAA0202)
    Bläser, S
    Jersch, K
    Hainmann, I
    Zieger, W
    Wunderle, D
    Busse, A
    Zieger, B
    [J]. GENE, 2003, 312 : 313 - 320
  • [3] Altered expression of the septin gene, SEPT9, in ovarian neoplasia
    Burrows, JF
    Chanduloy, S
    McIlhatton, MA
    Nagar, H
    Yeates, K
    Donaghy, P
    Price, J
    Godwin, AK
    Johnston, PG
    Russell, SHE
    [J]. JOURNAL OF PATHOLOGY, 2003, 201 (04) : 581 - 588
  • [4] SEPT9_v4 expression induces morphological change, increased motility and disturbed polarity
    Chacko, AD
    Hyland, PL
    McDade, SS
    Hamilton, PW
    Russell, SEH
    Hall, PA
    [J]. JOURNAL OF PATHOLOGY, 2005, 206 (04) : 458 - 465
  • [5] Cheon MS, 2001, J NEURAL TRANSM-SUPP, P311
  • [6] SEPT5_v2 is a parkin-binding protein
    Choi, P
    Snyder, H
    Petrucelli, L
    Theisler, C
    Chong, M
    Zhang, Y
    Lim, K
    Chung, KKK
    Kehoe, K
    D'Adamio, L
    Lee, JM
    Cochran, E
    Bowser, R
    Dawson, TM
    Wolozin, B
    [J]. MOLECULAR BRAIN RESEARCH, 2003, 117 (02): : 179 - 189
  • [7] Dopamine-dependent neurodegeneration in rats induced by viral vector-mediated overexpression of the parkin target protein, CDCrel-1
    Dong, ZZ
    Ferger, B
    Paterna, JC
    Vogel, D
    Furler, S
    Osinde, M
    Feldon, J
    Büeler, H
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2003, 100 (21) : 12438 - 12443
  • [8] Mitochondrial pro-apoptotic ARTS protein is lost in the majority of acute lymphoblastic leukemia patients
    Elhasid, R
    Sahar, D
    Merling, A
    Zivony, Y
    Rotem, A
    Ben-Arush, M
    Izraeli, S
    Bercovich, D
    Larisch, S
    [J]. ONCOGENE, 2004, 23 (32) : 5468 - 5475
  • [9] Aberrant protein expression in cerebral cortex of fetus with Down syndrome
    Engidawork, E
    Gulesserian, T
    Fountoulakis, M
    Lubec, G
    [J]. NEUROSCIENCE, 2003, 122 (01) : 145 - 154
  • [10] Septins: cytoskeletal polymers or signalling GTPases?
    Field, CM
    Kellogg, D
    [J]. TRENDS IN CELL BIOLOGY, 1999, 9 (10) : 387 - 394