TY - JOUR
T1 - The brain link protein-1 (BRAL1)
T2 - cDNA cloning, genomic structure, and characterization as a novel link protein expressed in adult brain
AU - Hirakawa, Satoshi
AU - Oohashi, Toshitaka
AU - Su, Wei Dong
AU - Yoshioka, Hidekatsu
AU - Murakami, Takuro
AU - Arata, Jirô
AU - Ninomiya, Yoshifumi
N1 - Funding Information:
We thank Drs. Uwe Rauch and Reinhard Fässler for continuous support and discussion throughout the study. We also thank Ms. Tomoko Yonezawa for critical review of the manuscript. This study was supported in part by a Grant-in-Aid from the Ministry of Education, Science, Sports, and Culture of Japan to Y.N. and by grants from the Kanae Foundation and Ryobi-Teien Foundation to T.O.
PY - 2000/10/5
Y1 - 2000/10/5
N2 - We report here molecular cloning and expression analysis of the gene for a novel human brain link protein-1 (BRAL1) which is predominantly expressed in brain. The predicted open reading frame of human brain link protein-1 encoded a polypeptide of 340 amino acids containing three protein modules, the immunoglobulin-like fold and proteoglycan tandem repeat 1 and 2 domains, with an estimated mass of 38 kDa. The brain link protein-1 mRNA was exclusively present in brain. When analyzed during mouse development, it was detected solely in the adult brain. Concomitant expression pattern of mRNAs for brain link protein-1 and various lectican proteoglycans in brain suggests a possibility that brain link protein-1 functions to stabilize the binding between hyaluronan and brevican. The human BRAL1 gene contained 7 exons and spanned ~6 kb. The entire immunoglobulin-like fold was encoded by a single exon and the proteoglycan tandem repeat 1 and 2 domains were encoded by a single and two exons, respectively. The deduced amino acid sequence of human brain link protein-1 exhibited 45% identity with human cartilage link protein-1 (CRTL1), previously reported as link protein to stabilize aggregates of aggrecan and hyaluronan in cartilage. These results suggest that brain link protein-1 may have distinct function from cartilage link protein-1 and play specific roles, especially in the adult brain. (C) 2000 Academic Press.
AB - We report here molecular cloning and expression analysis of the gene for a novel human brain link protein-1 (BRAL1) which is predominantly expressed in brain. The predicted open reading frame of human brain link protein-1 encoded a polypeptide of 340 amino acids containing three protein modules, the immunoglobulin-like fold and proteoglycan tandem repeat 1 and 2 domains, with an estimated mass of 38 kDa. The brain link protein-1 mRNA was exclusively present in brain. When analyzed during mouse development, it was detected solely in the adult brain. Concomitant expression pattern of mRNAs for brain link protein-1 and various lectican proteoglycans in brain suggests a possibility that brain link protein-1 functions to stabilize the binding between hyaluronan and brevican. The human BRAL1 gene contained 7 exons and spanned ~6 kb. The entire immunoglobulin-like fold was encoded by a single exon and the proteoglycan tandem repeat 1 and 2 domains were encoded by a single and two exons, respectively. The deduced amino acid sequence of human brain link protein-1 exhibited 45% identity with human cartilage link protein-1 (CRTL1), previously reported as link protein to stabilize aggregates of aggrecan and hyaluronan in cartilage. These results suggest that brain link protein-1 may have distinct function from cartilage link protein-1 and play specific roles, especially in the adult brain. (C) 2000 Academic Press.
KW - Brain
KW - Hyaluronan
KW - Lectican proteoglycan
KW - Link protein
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U2 - 10.1006/bbrc.2000.3583
DO - 10.1006/bbrc.2000.3583
M3 - Article
C2 - 11027579
AN - SCOPUS:0034610059
SN - 0006-291X
VL - 276
SP - 982
EP - 989
JO - Biochemical and Biophysical Research Communications
JF - Biochemical and Biophysical Research Communications
IS - 3
ER -