The challenge of Down syndrome

被引:92
作者
Antonarakis, Stylianos E.
Epstein, Charles J. [1 ]
机构
[1] Univ Calif San Francisco, Dept Pediat, San Francisco, CA 94143 USA
[2] Univ Calif San Francisco, Ctr Human Genet, San Francisco, CA 94143 USA
[3] Univ Geneva, Sch Med, Dept Genet Med & Dev, CH-1211 Geneva, Switzerland
[4] Univ Hosp Geneva, CH-1211 Geneva, Switzerland
关键词
D O I
10.1016/j.molmed.2006.08.005
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
Down syndrome (DS) has been recognized as a clinical entity for about 150 years, but it is only recently that there has been hope for the possibility to understand its pathogenesis and to use this information to devise approaches for the prevention and treatment of its numerous features. The earlier pessimism was due to several reasons, including: (i) the nature of the genetic defect that leads to the syndrome; (ii) the multiplicity of systems involved; and (iii) the high degree of variability of the phenotype. However, science has now caught up with the problem, and recent developments, especially in genetics, genomics, developmental biology and neuroscience, suggest that these potential impediments might not be as arduous as once appeared. As a result, basic research on DS is now rapidly accelerating, and there is hope that the findings will be translatable into benefit for people with DS.
引用
收藏
页码:473 / 479
页数:7
相关论文
共 80 条
[1]   Dosage-dependent over-expression of genes in the trisomic region of Ts1Cje mouse model for Down syndrome [J].
Amano, K ;
Sago, H ;
Uchikawa, C ;
Suzuki, T ;
Kotliarova, SE ;
Nukina, N ;
Epstein, CJ ;
Yamakawa, K .
HUMAN MOLECULAR GENETICS, 2004, 13 (13) :1333-1340
[2]  
Antonio A, 2004, J PROD ANAL, V21, P5
[3]   Measurement of locus copy number by hybridisation with amplifiable probes [J].
Armour, JAL ;
Sismani, C ;
Patsalis, PC ;
Cross, G .
NUCLEIC ACIDS RESEARCH, 2000, 28 (02) :605-609
[4]   NFAT dysregulation by increased dosage of DSCR1 and DYRK1A on chromosome 21 [J].
Arron, Joseph R. ;
Winslow, Monte M. ;
Polleri, Alberto ;
Chang, Ching-Pin ;
Wu, Hai ;
Gao, Xin ;
Neilson, Joel R. ;
Chen, Lei ;
Heit, Jeremy J. ;
Kim, Seung K. ;
Yamasaki, Nobuyuki ;
Miyakawa, Tsuyoshi ;
Francke, Uta ;
Graef, Isabella A. ;
Crabtree, Gerald R. .
NATURE, 2006, 441 (7093) :595-600
[5]   Cerebellar volume in adults with Down syndrome [J].
Aylward, EH ;
Habbak, R ;
Warren, AC ;
Pulsifer, MB ;
Barta, PE ;
Jerram, M ;
Pearlson, GD .
ARCHIVES OF NEUROLOGY, 1997, 54 (02) :209-212
[6]   Neuronal target genes of the neuron-restrictive silencer factor in neurospheres derived from fetuses with Down's syndrome: a gene expression study [J].
Bahn, S ;
Mimmack, M ;
Ryan, M ;
Caldwell, MA ;
Jaunlaux, E ;
Starkey, M ;
Svendsen, CN ;
Emson, P .
LANCET, 2002, 359 (9303) :310-315
[7]   Synaptic structural abnormalities in the Ts65Dn mouse model of Down syndrome [J].
Belichenko, PV ;
Masliah, E ;
Kleschevnikov, AM ;
Villar, AJ ;
Epstein, CJ ;
Salehi, A ;
Mobley, WC .
JOURNAL OF COMPARATIVE NEUROLOGY, 2004, 480 (03) :281-298
[8]   Cis-acting variation in the expression of a high proportion of genes in human brain [J].
Bray, NJ ;
Buckland, PR ;
Owen, MJ ;
O'Donovan, MC .
HUMAN GENETICS, 2003, 113 (02) :149-153
[9]   Natural variation in human gene expression assessed in lymphoblastoid cells [J].
Cheung, VG ;
Conlin, LK ;
Weber, TM ;
Arcaro, M ;
Jen, KY ;
Morley, M ;
Spielman, RS .
NATURE GENETICS, 2003, 33 (03) :422-425
[10]   The mouse brain transcriptome by SAGE: Differences in gene expression between P30 brains of the partial trisomy 16 mouse model of Down syndrome (Ts65Dn) and normals [J].
Chrast, R ;
Scott, HS ;
Papasavvas, MP ;
Rossier, C ;
Antonarakis, ES ;
Barras, C ;
Davisson, MT ;
Schmidt, C ;
Estivill, X ;
Dierssen, M ;
Pritchard, M ;
Antonarakis, SE .
GENOME RESEARCH, 2000, 10 (12) :2006-2021