Spatiotemporal expression of alternatively spliced IGF-I mRNA in the rat costochondral growth plate

被引:12
作者
Lin, WW [1 ]
Oberbauer, AM [1 ]
机构
[1] Univ Calif Davis, Dept Anim Sci, Davis, CA 95616 USA
关键词
D O I
10.1677/joe.0.1600461
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
IGF-I acts as a local proliferation and maturation factor for chondrocytes in the growth plate. However, the expression of different alternative IGF-I mRNA classes in the growth plate has not been characterized. Using quantitative reverse transcription PCR, the abundance of each alternative IGF-I mRNA class in resting, proliferative and hypertrophic chondrocytes was measured in rat costochondral growth plates. Class 1Ea mRNA was the most abundant IGF-I transcript overall and was highly expressed in proliferative chondrocytes at 2 and 4 weeks of age; by 6 weeks, the majority of 1Ea mRNA expression had shifted to hypertrophic chondrocytes. Class 1Eb mRNA was the second most abundant transcript and its distribution was uniform across all the cell types at 2 weeks of age. The expression pattern changed with increasing age such that at 6 weeks a gradient existed with hypertrophic chondrocytes expressing higher levels of 1Eb than resting chondrocytes. Class 2Ea mRNA was constitutively expressed at low levels across the: growth plate at all ages, while class 2Eb mRNA expression was negligible. The distribution of total IGF-I mRNA also shifted across growth plate cell types as the animals aged from 2 to 6 weeks. These finding; suggest that IGF-I class 1 mRNA plays the predominant role in the maturation of the growth plate.
引用
收藏
页码:461 / 467
页数:7
相关论文
共 28 条
[1]   INSULIN-LIKE GROWTH FACTOR-I MESSENGER RIBONUCLEIC-ACIDS WITH ALTERNATIVE 5'-UNTRANSLATED REGIONS ARE DIFFERENTIALLY EXPRESSED DURING DEVELOPMENT OF THE RAT [J].
ADAMO, M ;
LOWE, WL ;
LEROITH, D ;
ROBERTS, CT .
ENDOCRINOLOGY, 1989, 124 (06) :2737-2744
[2]   TRANSCRIPTION INITIATION IN THE 2 LEADER EXONS OF THE RAT IGF-I GENE OCCURS FROM DISPERSE VERSUS LOCALIZED SITES [J].
ADAMO, ML ;
BENHUR, H ;
LEROITH, D ;
ROBERTS, CT .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1991, 176 (02) :887-893
[3]   MURINE MACROPHAGES EXPRESS ABUNDANT INSULIN-LIKE GROWTH FACTOR-I CLASS-I EA AND EB TRANSCRIPTS [J].
ARKINS, S ;
REBEIZ, N ;
BIRAGYN, A ;
REESE, DL ;
KELLEY, KW .
ENDOCRINOLOGY, 1993, 133 (05) :2334-2343
[4]   NUCLEOTIDE-SEQUENCE OF A GENOMIC FRAGMENT OF THE RAT IGF-I GENE SPANNING AN ALTERNATE 5' NON-CODING EXON [J].
BUCCI, C ;
MALLUCCI, P ;
ROBERTS, CT ;
FRUNZIO, R ;
BRUNI, CB .
NUCLEIC ACIDS RESEARCH, 1989, 17 (09) :3596-3596
[5]  
CHOMCZYNSKI P, 1987, ANAL BIOCHEM, V162, P156, DOI 10.1016/0003-2697(87)90021-2
[6]   INSULIN-LIKE GROWTH FACTOR-I AND FACTOR-II - PEPTIDE, MESSENGER RIBONUCLEIC-ACID AND GENE STRUCTURES, SERUM, AND TISSUE CONCENTRATIONS [J].
DAUGHADAY, WH ;
ROTWEIN, P .
ENDOCRINE REVIEWS, 1989, 10 (01) :68-91
[7]   EFFECT OF GROWTH-HORMONE ON LEVELS OF DIFFERENTIALLY PROCESSED INSULIN-LIKE GROWTH FACTOR-I MESSENGER-RNAS IN TOTAL AND POLYSOMAL MESSENGER-RNA POPULATIONS [J].
FOYT, HL ;
LANAU, F ;
WOLOSCHAK, M ;
LEROITH, D ;
ROBERTS, CT .
MOLECULAR ENDOCRINOLOGY, 1992, 6 (11) :1881-1888
[8]   FUNCTIONAL-ANALYSIS OF THE RAT INSULIN-LIKE GROWTH FACTOR-I GENE AND IDENTIFICATION OF AN IGF-I GENE PROMOTER [J].
HALL, LJ ;
KAJIMOTO, Y ;
BICHELL, D ;
KIM, SW ;
JAMES, PL ;
COUNTS, D ;
NIXON, LJ ;
TOBIN, G ;
ROTWEIN, P .
DNA AND CELL BIOLOGY, 1992, 11 (04) :301-313
[9]  
Holthuizen E., 1991, MODERN CONCEPTS INSU, P733
[10]   ENGINEERING HYBRID GENES WITHOUT THE USE OF RESTRICTION ENZYMES - GENE-SPLICING BY OVERLAP EXTENSION [J].
HORTON, RM ;
HUNT, HD ;
HO, SN ;
PULLEN, JK ;
PEASE, LR .
GENE, 1989, 77 (01) :61-68