Osteocalcin is incompletely spliced in non-osseous tissues

被引:38
作者
Jung, CY
Ou, YC
Yeung, F
Frierson, HF
Kao, CH
机构
[1] Univ Virginia, Hlth Sci Ctr, Dept Urol, Mol Urol & Therapeut Program, Charlottesville, VA 22908 USA
[2] Univ Virginia, Hlth Sci Ctr, Dept Pathol, Charlottesville, VA 22908 USA
关键词
splicing; bone; intron retention; RNA transcript;
D O I
10.1016/S0378-1119(01)00513-3
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Osteocalcin (OC) is known to be a bone tissue-specific protein, expression of which is believed to be controlled by the OC promoter. In this communication, we provided evidence to demonstrate that tissue-specific expression of OC was also regulated at the RNA splicing level. We identified incompletely spliced variants of human OC mRNA, which retain one or more introns during RNA spicing, existing dominantly in non-osseous organs. Northern blot analysis identified two OC RNA transcripts expressed in normal human tissues. but the expression level of the transcripts varied between the tissues. Most non-osseous tissues expressed transcripts with higher molecular weight, prominent in ovary, kidney, pancreas, spleen, thymus, prostate, and testis, than the expected size of OC mRNA as seen in bone marrow. RT-PCR analysis identified up to six OC transcripts in most tissues tested except bone marrow. Sequence analysis showed that four of five RNA variants contained intron 1 in common and the dominant one contained all three introns. MG63, an osteoblastic osteosarcoma cell, expressed only the completely-spliced form of OC, whereas incompletely spliced RNA was dominant in most prostate tumor cells. Combined study of it? situ hybridization and immunohistochemistry revealed that OC RNA was highly expressed in prostate tumor epithelial cells while only very low levels of protein were detected, which confirms that there are OC RNA variants in non-osseous tissues. In conclusion, we demonstrated that OC mRNA is also expressed in several non-osseous tissues. However, only bone preferentially underwent the complete splicing event of all three introns. The function of other splicing variants of OC mRNA needs to be further investigated. (C) 2001 Published by Elsevier Science B.V. All rights reserved.
引用
收藏
页码:143 / 150
页数:8
相关论文
共 38 条
[21]  
Komminoth P, 1992, Diagn Mol Pathol, V1, P142, DOI 10.1097/00019606-199206000-00008
[22]   A ONE-STEP SANDWICH ENZYME-IMMUNOASSAY FOR GAMMA-CARBOXYLATED OSTEOCALCIN USING MONOCLONAL-ANTIBODIES [J].
KOYAMA, N ;
OHARA, K ;
YOKOTA, H ;
KUROME, T ;
KATAYAMA, M ;
HINO, F ;
KATO, I ;
AKAI, T .
JOURNAL OF IMMUNOLOGICAL METHODS, 1991, 139 (01) :17-23
[23]   STRUCTURE OF THE RAT OSTEOCALCIN GENE AND REGULATION OF VITAMIN-D-DEPENDENT EXPRESSION [J].
LIAN, J ;
STEWART, C ;
PUCHACZ, E ;
MACKOWIAK, S ;
SHALHOUB, V ;
COLLART, D ;
ZAMBETTI, G ;
STEIN, G .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1989, 86 (04) :1143-1147
[24]  
Lian JB, 1998, J CELL BIOCHEM, P62, DOI 10.1002/(SICI)1097-4644(1998)72:30/31+<62::AID-JCB10>3.0.CO
[25]  
2-S
[26]   Spontaneous calcification of arteries and cartilage in mice lacking matrix GLA protein [J].
Luo, GB ;
Ducy, P ;
McKee, MD ;
Pinero, GJ ;
Loyer, E ;
Behringer, RR ;
Karsenty, G .
NATURE, 1997, 386 (6620) :78-81
[27]   THE GENERALLY EXPRESSED HNRNP-F IS INVOLVED IN A NEURAL-SPECIFIC PRE-MESSENGER-RNA SPLICING EVENT [J].
MIN, HS ;
CHAN, RC ;
BLACK, DL .
GENES & DEVELOPMENT, 1995, 9 (21) :2659-2671
[28]  
O'Keefe DS, 1998, BBA-GENE STRUCT EXPR, V1443, P113
[29]  
POSER JW, 1980, J BIOL CHEM, V255, P8685
[30]   MULTIPLE COPIES OF THE BONE-SPECIFIC OSTEOCALCIN GENE IN MOUSE AND RAT [J].
RAHMAN, S ;
OBERDORF, A ;
MONTECINO, M ;
TANHAUSER, SM ;
LIAN, JB ;
STEIN, GS ;
LAIPIS, PJ ;
STEIN, JL .
ENDOCRINOLOGY, 1993, 133 (06) :3050-3053