Expression profiling of human fetal growth plate cartilage by EST sequencing

The differentiation of mesenchymal stem cells into hypertrophic chondrocytes is an integral and multistep process important in pattern formation, endochondral ossification, and postnatal growth of the skeleton. In recent years, novel genes involved in these processes have been identified, but still...

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Published in:Matrix biology Vol. 24; no. 8; pp. 530 - 538
Main Authors: Tagariello, Andreas, Schlaubitz, Silke, Hankeln, Thomas, Mohrmann, Gerrit, Stelzer, Christiane, Schweizer, Anja, Hermanns, Pia, Lee, Brendan, Schmidt, Erwin R., Winterpacht, Andreas, Zabel, Bernhard
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Language:English
Published: Netherlands Elsevier B.V 01-12-2005
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Abstract The differentiation of mesenchymal stem cells into hypertrophic chondrocytes is an integral and multistep process important in pattern formation, endochondral ossification, and postnatal growth of the skeleton. In recent years, novel genes involved in these processes have been identified, but still only little is known about the large-scale gene expression profile during skeletal development. We initiated an expressed sequence tag (EST) project aiming at the identification of genes and pathways involved in this complex process. Candidate genes are expected to be of value for diagnosis and treatment of monogenic and multigenic heritable disorders of the skeleton. Here, we describe the sequences of 4748 clones from a human growth plate cartilage cDNA library generated from 20 weeks prenatal–2 years postnatal specimens. In silico analysis of these sequences revealed 1688 individual transcription units, corresponding to known (1274) and to novel, yet uncharacterised potential genes (414). The tissue specificity of the library was reflected by its corresponding EST profile representing a total of ∼10% proteins already shown to be involved in cartilage/bone development or homeostasis. The EST profile also reflects the developmental stage of the tissue with significant differences in the expression of matrix proteins compared to corresponding EST profiles from 8–12 and 12–20 week human fetal cartilage. Calculation of the relative frequency of transcripts in our cDNA library, as compared to their abundance in other EST datasets, revealed a set of ∼200 genes, including 81 novel, yet uncharacterised genes, showing increased expression. These genes represent candidates for the large number of osteochondrodysplasias for which the causative gene defects have not yet been identified.
AbstractList The differentiation of mesenchymal stem cells into hypertrophic chondrocytes is an integral and multistep process important in pattern formation, endochondral ossification, and postnatal growth of the skeleton. In recent years, novel genes involved in these processes have been identified, but still only little is known about the large-scale gene expression profile during skeletal development. We initiated an expressed sequence tag (EST) project aiming at the identification of genes and pathways involved in this complex process. Candidate genes are expected to be of value for diagnosis and treatment of monogenic and multigenic heritable disorders of the skeleton. Here, we describe the sequences of 4,748 clones from a human growth plate cartilage cDNA library generated from 20 weeks prenatal-2 years postnatal specimens. In silico analysis of these sequences revealed 1,688 individual transcription units, corresponding to known (1,274) and to novel, yet uncharacterised potential genes (414). The tissue specificity of the library was reflected by its corresponding EST profile representing a total of approximately 10% proteins already shown to be involved in cartilage/bone development or homeostasis. The EST profile also reflects the developmental stage of the tissue with significant differences in the expression of matrix proteins compared to corresponding EST profiles from 8-12 and 12-20 week human fetal cartilage. Calculation of the relative frequency of transcripts in our cDNA library, as compared to their abundance in other EST datasets, revealed a set of approximately 200 genes, including 81 novel, yet uncharacterised genes, showing increased expression. These genes represent candidates for the large number of osteochondrodysplasias for which the causative gene defects have not yet been identified.
The differentiation of mesenchymal stem cells into hypertrophic chondrocytes is an integral and multistep process important in pattern formation, endochondral ossification, and postnatal growth of the skeleton. In recent years, novel genes involved in these processes have been identified, but still only little is known about the large-scale gene expression profile during skeletal development. We initiated an expressed sequence tag (EST) project aiming at the identification of genes and pathways involved in this complex process. Candidate genes are expected to be of value for diagnosis and treatment of monogenic and multigenic heritable disorders of the skeleton. Here, we describe the sequences of 4748 clones from a human growth plate cartilage cDNA library generated from 20 weeks prenatal–2 years postnatal specimens. In silico analysis of these sequences revealed 1688 individual transcription units, corresponding to known (1274) and to novel, yet uncharacterised potential genes (414). The tissue specificity of the library was reflected by its corresponding EST profile representing a total of ∼10% proteins already shown to be involved in cartilage/bone development or homeostasis. The EST profile also reflects the developmental stage of the tissue with significant differences in the expression of matrix proteins compared to corresponding EST profiles from 8–12 and 12–20 week human fetal cartilage. Calculation of the relative frequency of transcripts in our cDNA library, as compared to their abundance in other EST datasets, revealed a set of ∼200 genes, including 81 novel, yet uncharacterised genes, showing increased expression. These genes represent candidates for the large number of osteochondrodysplasias for which the causative gene defects have not yet been identified.
Author Hankeln, Thomas
Mohrmann, Gerrit
Schlaubitz, Silke
Stelzer, Christiane
Schmidt, Erwin R.
Hermanns, Pia
Lee, Brendan
Tagariello, Andreas
Winterpacht, Andreas
Schweizer, Anja
Zabel, Bernhard
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  givenname: Gerrit
  surname: Mohrmann
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  givenname: Christiane
  surname: Stelzer
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  surname: Lee
  fullname: Lee, Brendan
  organization: Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX 77030, USA
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  givenname: Erwin R.
  surname: Schmidt
  fullname: Schmidt, Erwin R.
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  givenname: Bernhard
  surname: Zabel
  fullname: Zabel, Bernhard
  organization: Children's Hospital, University of Mainz, Langenbeckstr. 1, D-55101-Mainz, Germany
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Skeletal development
Expression profiling
ESTs
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SSID ssj0004478
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Snippet The differentiation of mesenchymal stem cells into hypertrophic chondrocytes is an integral and multistep process important in pattern formation, endochondral...
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SubjectTerms ESTs
Expressed Sequence Tags
Expression profiling
Extracellular Matrix Proteins - genetics
Fetus - metabolism
Gene Expression Profiling
Gene Expression Regulation, Developmental - genetics
Growth plate
Growth Plate - embryology
Growth Plate - metabolism
Humans
Proteoglycans - genetics
Skeletal development
Title Expression profiling of human fetal growth plate cartilage by EST sequencing
URI https://dx.doi.org/10.1016/j.matbio.2005.08.002
https://www.ncbi.nlm.nih.gov/pubmed/16176871
https://search.proquest.com/docview/68864998
Volume 24
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