Second cysteine-rich region of epidermal growth factor receptor contains targeting information for caveolae/rafts

被引:98
作者
Yamabhai, M [1 ]
Anderson, RGW [1 ]
机构
[1] Univ Texas, SW Med Ctr, Dept Cell Biol, Dallas, TX 75235 USA
关键词
D O I
10.1074/jbc.C200277200
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
Previous studies have shown that similar to60% of the epidermal growth factor receptors (EGFRs) in quiescent fibroblasts are concentrated in the caveolae/raft fraction from purified plasma membranes. This high degree of localization suggests the EGFR contains targeting information for lipid domains. We have used mutagenesis to determine that the region of the receptor that controls targeting to caveolae/rafts resides in the juxtamembrane, second cysteine-rich region. A 60-amino acid-long sequence within this region that is continuous with the transmembrane domain was sufficient to target the transmembrane and cytoplasmic tails of both EGFR and the low density lipoprotein receptor to caveolae/rafts. Two N-linked sugars in this segment were not required for proper targeting, although unglycosylated wild-type receptors did not localize property. We conclude that, in contrast to signals for coated pit localization that are in the cytoplasmic tail, the targeting information for caveolae/rafts is on the extracellular side of the EGFR very close to the membrane.
引用
收藏
页码:24843 / 24846
页数:4
相关论文
共 22 条
[1]  
ALEXANDER S, 1998, FRONT BIOSCI, V3, pD729
[2]   Analysis of the transmembrane domain of influenza virus neuraminidase, a type II transmembrane glycoprotein, for apical sorting and raft association [J].
Barman, S ;
Nayak, DP .
JOURNAL OF VIROLOGY, 2000, 74 (14) :6538-6545
[3]   SORTING OF GPI-ANCHORED PROTEINS TO GLYCOLIPID-ENRICHED MEMBRANE SUBDOMAINS DURING TRANSPORT TO THE APICAL CELL-SURFACE [J].
BROWN, DA ;
ROSE, JK .
CELL, 1992, 68 (03) :533-544
[4]  
Carpenter G, 2000, BIOESSAYS, V22, P697, DOI 10.1002/1521-1878(200008)22:8<697::AID-BIES3>3.3.CO
[5]  
2-T
[6]   EGF RECEPTOR AND ERBB-2 TYROSINE KINASE DOMAINS CONFER CELL SPECIFICITY FOR MITOGENIC SIGNALING [J].
DIFIORE, PP ;
SEGATTO, O ;
TAYLOR, WG ;
AARONSON, SA ;
PIERCE, JH .
SCIENCE, 1990, 248 (4951) :79-83
[7]   CLOSE SIMILARITY OF EPIDERMAL GROWTH-FACTOR RECEPTOR AND V-ERB-B ONCOGENE PROTEIN SEQUENCES [J].
DOWNWARD, J ;
YARDEN, Y ;
MAYES, E ;
SCRACE, G ;
TOTTY, N ;
STOCKWELL, P ;
ULLRICH, A ;
SCHLESSINGER, J ;
WATERFIELD, MD .
NATURE, 1984, 307 (5951) :521-527
[8]   Guidance of cell migration by EGF receptor signaling during Drosophila oogenesis [J].
Duchek, P ;
Rorth, P .
SCIENCE, 2001, 291 (5501) :131-133
[9]   Glycosylation-induced conformational modification positively regulates receptor-receptor association -: A study with an aberrant epidermal growth factor receptor (EGFRvIII/ΔEGFR) expressed in cancer cells [J].
Fernandes, H ;
Cohen, S ;
Bishayee, S .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2001, 276 (07) :5375-5383
[10]   Structural determinants required for apical sorting of an intestinal brush-border membrane protein [J].
Jacob, R ;
Alfalah, M ;
Grünberg, J ;
Obendorf, M ;
Naim, HY .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2000, 275 (09) :6566-6572