Fetuin-B, a second member of the fetuin family in mammals

被引:131
作者
Olivier, E
Soury, E
Ruminy, P
Husson, A
Parmentier, F
Daveau, M
Salier, JP
机构
[1] Fac Med Pharm, INSERM, U519, F-76183 Rouen, France
[2] Fac Med Pharm, Inst Federat Rech Multidisciplinaires Peptides, F-76183 Rouen, France
[3] Fac Med Pharm, Appareii Digest Environm & Nutr Res Grp, Rouen, France
[4] Fac Med Pharm, INSERM, EPI 9906, Rouen, France
关键词
acute inflammation; cystatin superfamily; development; liver; alpha; 2-HS-glycoprotein;
D O I
10.1042/0264-6021:3500589
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
A set of orthologous plasma proteins found in human, sheep, pig, cow and rodents, now collectively designated fetuin-A, constitutes the fetuin family. Fetuin-A has been identified as a major protein during fetal life and is also involved in important functions such as inhibition of the insulin receptor tyrosine kinase activity, protease inhibitory activities and development-associated regulation of calcium metabolism and osteogenesis. Furthermore, fetuin-A is a key partner in the recovery phase of an acute inflammatory response. We now describe a second protein of the fetuin family, called fetuin-B, which is found at least in human and rodents. On grounds of domain homology, overall conservation of cysteine residues and chromosomal assignments of the corresponding genes in these species, fetuin-B is unambiguously a paralogue of fetuin-A. Yet, fetuin-A and fetuin-B exhibit significant differences at the amino acid sequence level, notably including variations with respect to the archetypal fetuin-specific signature. Differences and similarities in terms of gene regulation were also observed. Indeed, studies performed during development in rat and mouse showed for the first time high expression of a member of the fetuin family in adulthood, as shown with the fetuin-B mRNA in rat. However, like its fetuin-A counterpart, the fetuin-B mRNA level is down-regulated during the acute phase of experimentally induced inflammation in rat.
引用
收藏
页码:589 / 597
页数:9
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