Neonatal growth cartilage: Equine tissue specific gene expression

Biochemical and Biophysical Research Communications

Volumn 354, Issue 4, 2007, Pages 975-980

  Johannessen, Maria Kjeldaas ^a   Skretting, Grethe ^b   Ytrehus, Bjørnar ^c   Røed, Knut H ^a  

^a NORWEGIAN UNIVERSITY OF LIFE SCIENCES   (Norway)

^b ULLEVÅL UNIVERSITY HOSPITAL   (Norway)

^c NORWEGIAN VETERINARY INSTITUTE   (Norway)

Author keywords

Endochondral bone formation; EST; Gene expression; Growth cartilage; Horse; SSH

Indexed keywords

ACID PROTEIN; ANGIOPOIETIN; COMPLEMENTARY DNA; CYTOKINE; FUNCTIONAL GROUP; GROWTH FACTOR;

ANIMAL TISSUE; ARTICLE; ARTICULAR CARTILAGE; CARTILAGE; CONTROLLED STUDY; DNA LIBRARY; EPIPHYSEAL CARTILAGE; EXTRACELLULAR MATRIX; FEMALE; FOAL; GENE EXPRESSION; GENE FUNCTION; GENE IDENTIFICATION; GENETIC ANALYSIS; HORSE; HYBRIDIZATION; MOLECULAR CLONING; NONHUMAN; NORTHERN BLOTTING; NUCLEOTIDE SEQUENCE; PRIORITY JOURNAL; SIGNAL TRANSDUCTION; TISSUE DISTRIBUTION; TISSUE SPECIFICITY; TRANSCRIPTION INITIATION;

EQUIDAE;

EID: 33846817263     PISSN: 0006291X     EISSN: 10902104     Source Type: Journal    
DOI: 10.1016/j.bbrc.2007.01.074     Document Type: Article

References (39)

1. Kronenberg H.M. Developmental regulation of the growth plate. Nature 423 (2003) 332-336
2. Provot S., and Schipani E. Molecular mechanisms of endochondral bone development. Biochem. Biophys. Res. Commun. 328 (2005) 658-665
3. Hall C.M. International nosology and classification of constitutional disorders of bone (2001). Am. J. Med. Genet. 113 (2002) 65-77
4. Kornak U., and Mundlos S. Genetic disorders of the skeleton: a developmental approach. Am. J. Hum. Genet. 73 (2003) 447-474
5. Weisbrode S.E. Bone and joints. In: McGavin M.C., and Zachary J.F. (Eds). Pathologic Basis of Veterinary Disease (2007), Mosby, St. Louis 1041-1105
6. Alberts B., Johnson A., Lewis J., Raff M., Roberts K., and Walter P. Manipulating proteins DNA and RNA. In: Alberts B., Johnson A., Lewis J., Raff M., Roberts K., and Walter P. (Eds). Molecular Biology of the Cell (2002), Garland Science, New York 469-546
7. Alberts B., Johnson A., Lewis J., Raff M., Roberts K., and Walter P. Control of gene expression. In: Alberts B., Johnson A., Lewis J., Raff M., Roberts K., and Walter P. (Eds). Molecular Biology of the Cell (2002), Garland Science, New York 375-468
8. Zelzer E., and Olsen B.R. The genetic basis for skeletal diseases. Nature 423 (2003) 343-348
9. Ekman S., Rodriguez-Martinez H., and Ploen L. Morphology of normal and osteochondrotic porcine articular-epiphyseal cartilage. A study in the domestic pig and minipig of wild hog ancestry. Acta Anat. (Basel) 139 (1990) 239-253
10. Ekman S., and Carlson C.S. The pathophysiology of osteochondrosis. Vet. Clin. N. Am. Small Anim. Pract. 28 (1998) 17-32
11. Okihana H., and Yamada K. Preparation of a cDNA library and preliminary assessment of 1400 genes from mouse growth cartilage. J. Bone Miner. Res. 14 (1999) 304-310
12. Zhang H., Marshall K.W., Tang H., Hwang D.M., Lee M., and Liew C.C. Profiling genes expressed in human fetal cartilage using 13,155 expressed sequence tags. Osteoarthr. Cartil. 11 (2003) 309-319
13. Krakow D., Sebald E.T., Pogue R., Rimoin L.P., King L., and Cohn D.H. Analysis of clones from a human cartilage cDNA library provides insight into chondrocyte gene expression and identifies novel candidate genes for the osteochondrodysplasias. Mol. Genet. Metab. 79 (2003) 34-42
14. Pogue R., Sebald E., King L., Kronstadt E., Krakow D., and Cohn D.H. A transcriptional profile of human fetal cartilage. Matrix Biol. 23 (2004) 299-307
15. Tagariello A., Schlaubitz S., Hankeln T., Mohrmann G., Stelzer C., Schweizer A., et al. Expression profiling of human fetal growth plate cartilage by EST sequencing. Matrix Biol. 24 (2005) 530-538
16. Tollet-Egnell P., Flores-Morales A., Odeberg J., Lundeberg J., and Norstedt G. Differential cloning of growth hormone-regulated hepatic transcripts in the aged rat. Endocrinology 141 (2000) 910-921
17. Skretting G., Espenes A., Ulvund M.J., and Olsaker I. cDNA representational difference analysis of ileal Peyer's patches in lambs after oral inoculation with scrapie. Biochem. Biophys. Res. Commun. 316 (2004) 272-279
18. Ochi K., Derfoul A., and Tuan R.S. A predominantly articular cartilage-associated gene, SCRG1, is induced by glucocorticoid and stimulates chondrogenesis in vitro. Osteoarthr. Cartil. 14 (2006) 30-38
19. Wang Y., Middleton F., Horton J.A., Reichel L., Farnum C.E., and Damron T.A. Microarray analysis of proliferative and hypertrophic growth plate zones identifies differentiation markers and signal pathways. Bone 35 (2004) 1273-1293
20. Schmid T.M., and Linsenmayer T.F. A short chain (pro)collagen from aged endochondral chondrocytes. Biochemical characterization. J. Biol. Chem. 258 (1983) 9504-9509
21. Chen J., Zhang Q., McCulloch C.A., and Sodek J. Immunohistochemical localization of bone sialoprotein in foetal porcine bone tissues: comparisons with secreted phosphoprotein 1 (SPP-1, osteopontin) and SPARC (osteonectin). Histochem. J. 23 (1991) 281-289
22. Natsume W., Tanabe K., Kon S., Yoshida N., Watanabe T., Torii T., et al. SMAP2, a novel ARF GTPase-activating protein, interacts with clathrin and clathrin assembly protein and functions on the AP-1-positive early endosome/trans-Golgi network. Mol. Biol. Cell 17 (2006) 2592-2603
23. Oike Y., Yasunaga K., and Suda T. Angiopoietin-related/angiopoietin-like proteins regulate angiogenesis. Int. J. Hematol. 80 (2004) 21-28
24. Vu T.H., Shipley J.M., Bergers G., Berger J.E., Helms J.A., Hanahan D., et al. MMP-9/gelatinase B is a key regulator of growth plate angiogenesis and apoptosis of hypertrophic chondrocytes. Cell 93 (1998) 411-422
25. Gerber H.P., Vu T.H., Ryan A.M., Kowalski J., Werb Z., and Ferrara N. VEGF couples hypertrophic cartilage remodeling, ossification and angiogenesis during endochondral bone formation. Nat. Med. 5 (1999) 623-628
26. Carlson C.S., Hilley H.D., and Meuten D.J. Degeneration of cartilage canal vessels associated with lesions of osteochondrosis in swine. Vet. Pathol. 26 (1989) 47-54
27. Carlson C.S., Cullins L.D., and Meuten D.J. Osteochondrosis of the articular-epiphyseal cartilage complex in young horses: evidence for a defect in cartilage canal blood supply. Vet. Pathol. 32 (1995) 641-647
28. Ytrehus B., Ekman S., Carlson C.S., Teige J., and Reinholt F.P. Focal changes in blood supply during normal epiphyseal growth are central in the pathogenesis of osteochondrosis in pigs. Bone 35 (2004) 1294-1306
29. Katoh Y., and Katoh M. Comparative integromics on Angiopoietin family members. Int. J. Mol. Med. 17 (2006) 1145-1149
30. Klyce S.D., and Beuerman R.W. Structure and function of the cornea. In: Kaufman H.E., Barron B.A., McDonald M.B., and Waltman S.R. (Eds). The cornea (1988), Churchill Livingstone, New York 3-54
31. Trueta J. The normal vascular anatomy of the human femoral head during growth. J. Bone Joint Surg. Br. 39-B (1957) 358-394
32. Hsu D.R., Economides A.N., Wang X., Eimon P.M., and Harland R.M. The Xenopus dorsalizing factor Gremlin identifies a novel family of secreted proteins that antagonize BMP activities. Mol. Cell 1 (1998) 673-683
33. Urist M.R. Bone: formation by autoinduction. Science 150 (1965) 893-899
34. Sakou T. Bone morphogenic proteins: from basic studies to clinical approaches. Bone 22 (1998) 306-591
35. Brunet L.J., McMahon J.A., McMahon A.P., and Harland R.M. Noggin, cartilage morphogenesis, and joint formation in the mammalian skeleton. Science 280 (1998) 1455-1457
36. Semevolos S.A., Nixon A.J., and Strassheim M.L. Expression of bone morphogenetic protein-6 and -2 and a bone morphogenetic protein antagonist in horses with naturally acquired osteochondrosis. Am. J. Vet. Res. 65 (2004) 110-115
37. Chen B., Athanasiou M., Gu Q., and Blair D.G. Drm/Gremlin transcriptionally activates p21(Cip1) via a novel mechanism and inhibits neoplastic transformation. Biochem. Biophys. Res. Commun. 295 (2002) 1135-1141
38. Ohyama A., Saito F., Ohuchi H., and Noji S. Differential expression of two BMP antagonists, gremlin and Follistatin, during development of the chick feather bud. Mech. Dev. 100 (2001) 331-333
39. Capdevila J., Tsukui T., Rodriquez E.C., Zappavigna V., and Izpisua Belmonte J.C. Control of vertebrate limb outgrowth by the proximal factor Meis2 and distal antagonism of BMPs by Gremlin. Mol. Cell 4 (1999) 839-849