Cloning of a novel cDNA expressed during the early stages of fracture healing

被引:26
作者
Hadjiargyrou, M [1 ]
Halsey, MF
Ahrens, W
Rightmire, EP
McLeod, KJ
Rubin, CT
机构
[1] SUNY Stony Brook, Biomed Engn Program, Musculoskeletal Res Lab, Stony Brook, NY 11794 USA
[2] SUNY Stony Brook, Dept Orthopaed, Musculoskeletal Res Lab, Stony Brook, NY 11794 USA
关键词
differential mRNA display; bone; gene expression;
D O I
10.1006/bbrc.1998.9167
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
Using differential mRNA display (DD-PCR), a novel cDNA, FxC1 (Fracture Callus 1) was isolated from the early stages of a healing fractured femur. Utilizing 5' RACE PCR, a 598-bp full-length cDNA was obtained for FxC1 that contains an open reading frame (ORF) of 243 bp, encoding for an 80 amino acid protein. Within this ORF, a leucine zipper motif was present. In vitro transcription/translation of the full-length cDNA generated the expected 9-kDa protein. Northern analysis reveals that this gene is expressed in calluses harvested from post-fracture day 5, 7 and 10, as well as in several other tissues and bone-derived cell lines. During the differentiation of MC3T3 cells along the osteoblast lineage, FxC1 expression increases 3- to 4-fold during the production and deposition of matrix proteins, suggesting a possible role for this protein in cell differentiation. (C) 1998 Academic Press.
引用
收藏
页码:879 / 884
页数:6
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