Differential expression of genes associated with collagen fibril growth in the chicken tendon: Identification of structural and regulatory genes by subtractive hybridization

被引:28
作者
Nurminskaya, MV [1 ]
Birk, DE [1 ]
机构
[1] Tufts Univ, Sch Med, Dept Anat & Cellular Biol, Boston, MA 02111 USA
关键词
subtractive hybridization; chicken tendon development; collagen fibril growth;
D O I
10.1006/abbi.1997.0498
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
Collagen fibril growth is a very rapid and abrupt process, resulting in a 4- to 5-fold increase in fibril length between 16 and 18 days of chicken metatarsal tendon development. This fibril growth is due to a postdepositional fusion/association of preformed intermediates, termed fibril segments. We propose that the regulated assembly of collagen fibrils from the segment intermediates is mediated by interactions of structural macromolecules. The cells could modulate this process by responding to cytokines and altering cell-matrix signaling, transcription, and translation. To identify the genes involved in this process a subtractive hybridization procedure was utilized. Genes of cell proliferation were excluded as major contributors to differential gene expression in avian tendon on days 14 and 19 of development after analysis of BrdUr incorporation. The BrdUr incorporation studies revealed little, if any, tendon fibroblast proliferation at both stages. This suggested that observed alterations in gene expression would be related to the pre- and postfibril growth phases in developing tendons. A total of 80 unique up- and down-regulated cDNA fragments were isolated and 26 of these were identified. There was an up-regulation of structural proteins (for example, collagen types I, VI, and XI and fibromodulin), a number of regulatory proteins (including TGF-beta 2 and IGF-1), as well as other enzymes/proteins. Northern analysis confirmed the up-regulation of mRNAs for all the structural proteins, The observed 20-fold increase of mRNA for the isolated clone corresponding to the 3' UTR of alpha 1(VI) collagen makes it a possible marker for the postfibril growth stage of collagen fibrillogenesis. The large number of isolated genes differentially expressed during the rapid phase of fibril growth reveals a fine and possibly tissue-specific control of fibrillogenesis. (C) 1998 Academic Press.
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页码:1 / 9
页数:9
相关论文
共 52 条
[1]   LONG-TERM EXPLANT CULTURE OF RABBIT FLEXOR TENDON - EFFECTS OF RECOMBINANT HUMAN INSULIN-LIKE GROWTH FACTOR-I AND SERUM ON MATRIX METABOLISM [J].
ABRAHAMSSON, SO ;
LUNDBORG, G ;
LOHMANDER, LS .
JOURNAL OF ORTHOPAEDIC RESEARCH, 1991, 9 (04) :503-515
[2]  
Birk D., 1991, CELL BIOLOPY EXTRACE, V2nd, P221
[3]  
Birk D.E., 1994, EXTRACELL MATRIX ASS, P91, DOI [10.1016/b978-0-12-775170-2.50009-3, DOI 10.1016/B978-0-12-775170-2.50009-3]
[4]   COLLAGEN FIBRILLOGENESIS IN-SITU - FIBRIL SEGMENTS UNDERGO POSTDEPOSITIONAL MODIFICATIONS RESULTING IN LINEAR AND LATERAL GROWTH DURING MATRIX DEVELOPMENT [J].
BIRK, DE ;
NURMINSKAYA, MV ;
ZYCBAND, EI .
DEVELOPMENTAL DYNAMICS, 1995, 202 (03) :229-243
[5]  
Birk DE, 1997, EUR J CELL BIOL, V72, P352
[6]  
BIRK DE, 1994, J ANAT, V184, P457
[7]   EXTRACELLULAR COMPARTMENTS IN TENDON MORPHOGENESIS - COLLAGEN FIBRIL, BUNDLE, AND MACROAGGREGATE FORMATION [J].
BIRK, DE ;
TRELSTAD, RL .
JOURNAL OF CELL BIOLOGY, 1986, 103 (01) :231-240
[8]  
Birk DE, 1997, DEV DYNAM, V208, P291
[9]   Characterization of collagen fibril segments from chicken embryo cornea, dermis and tendon [J].
Birk, DE ;
Hahn, RA ;
Linsenmayer, CY ;
Zycband, EI .
MATRIX BIOLOGY, 1996, 15 (02) :111-118
[10]   COLLAGEN FIBRILLOGENESIS INSITU - FIBRIL SEGMENTS ARE INTERMEDIATES IN MATRIX ASSEMBLY [J].
BIRK, DE ;
ZYCBAND, EI ;
WINKELMANN, DA ;
TRELSTAD, RL .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1989, 86 (12) :4549-4553