Variations in gene expression among different types of human skeletal muscle

被引:27
作者
Kang, PB
Kho, AT
Sanoudou, D
Haslett, JN
Dow, CP
Han, M
Blasko, JM
Lidov, HGW
Beggs, AH
Kunkel, LM
机构
[1] Howard Hughes Med Inst, Genom Program, Boston, MA 02115 USA
[2] Harvard Univ, Childrens Hosp Boston, Sch Med, Dept Neurol, Boston, MA 02115 USA
[3] Harvard Univ, Sch Med, Childrens Hosp, Informat Program, Boston, MA 02115 USA
[4] Acad Athens, Fdn Biomed Res, Athens, Greece
[5] Harvard Univ, Childrens Hosp Boston, Sch Med, Dept Pathol, Boston, MA USA
关键词
aging; gene expression; muscle; muscular dystrophy;
D O I
10.1002/mus.20356
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
There is a consistent variation in the response of different skeletal muscle groups to mutations in genes known to cause muscular dystrophy, yet these muscles appear histologically similar. To better understand these phenotypic differences, we analyzed gene expression patterns in control muscle specimens obtained from four sites at autopsy: deltoid, quadriceps, gastrocnemius, and tibialis anterior (TA). A total of 35 muscle samples from nine individuals (four pediatric and five geriatric) were studied. Factors potentially influencing gene expression in the different samples included individuality, age, muscle type, gender, cause of death, postmortem interval, and ethnicity. The first three factors, in decreasing order, were found to have a significant impact on the stratification of muscle specimens. A novel analytic method, using a second round of normalization, was used to elicit differences between muscle types. This approach may be extended to a broader survey, potentially elucidating a molecular classification of the skeletal muscles.
引用
收藏
页码:483 / 491
页数:9
相关论文
共 33 条
[1]
FatiGO:: a web tool for finding significant associations of Gene Ontology terms with groups of genes [J].
Al-Shahrour, F ;
Díaz-Uriarte, R ;
Dopazo, J .
BIOINFORMATICS, 2004, 20 (04) :578-580
[2]
A web-accessible complete transcriptome of normal human and DMD muscle [J].
Bakay, M ;
Zhao, P ;
Chen, J ;
Hoffman, EP .
NEUROMUSCULAR DISORDERS, 2002, 12 :S125-S141
[3]
Defective membrane repair in dysferlin-deficient muscular dystrophy [J].
Bansal, D ;
Miyake, K ;
Vogel, SS ;
Groh, S ;
Chen, CC ;
Williamson, R ;
McNeil, PL ;
Campbell, KP .
NATURE, 2003, 423 (6936) :168-172
[4]
HISTOGRAPHIC ANALYSIS OF HUMAN MUSCLE BIOPSIES WITH REGARD TO FIBER TYPES .4. CHILDRENS BIOPSIES [J].
BROOKE, MH ;
ENGEL, WK .
NEUROLOGY, 1969, 19 (06) :591-+
[5]
A CDNA CLONE FROM THE DUCHENNE BECKER MUSCULAR-DYSTROPHY GENE [J].
BURGHES, AHM ;
LOGAN, C ;
HU, XY ;
BELFALL, B ;
WORTON, RG ;
RAY, PN .
NATURE, 1987, 328 (6129) :434-437
[6]
Differential global gene expression in red and white skeletal muscle [J].
Campbell, WG ;
Gordon, SE ;
Carlson, CJ ;
Pattison, JS ;
Hamilton, MT ;
Booth, FW .
AMERICAN JOURNAL OF PHYSIOLOGY-CELL PHYSIOLOGY, 2001, 280 (04) :C763-C768
[7]
Constitutive activation of MAPK cascade in acute quadriplegic myopathy [J].
Di Giovanni, S ;
Molon, A ;
Broccolini, A ;
Melcon, G ;
Mirabella, M ;
Hoffman, EP ;
Servidei, S .
ANNALS OF NEUROLOGY, 2004, 55 (02) :195-206
[8]
EDSTROM L, 1969, ACTA NEUROL SCAND, V45, P257
[9]
Cluster analysis and display of genome-wide expression patterns [J].
Eisen, MB ;
Spellman, PT ;
Brown, PO ;
Botstein, D .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1998, 95 (25) :14863-14868
[10]
MEMBRANE ORGANIZATION OF THE DYSTROPHIN-GLYCOPROTEIN COMPLEX [J].
ERVASTI, JM ;
CAMPBELL, KP .
CELL, 1991, 66 (06) :1121-1131