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Altenberger, T; Bilban, M; Auer, M; Knosp, E; Wolfsberger, S; Gartner, W; Mineva, I; Zielinski, C; Wagner, L; Luger, A.
Identification of DLK1 variants in pituitary- and neuroendocrine tumors.
Biochem Biophys Res Commun. 2006; 340(3):995-1005 Doi: 10.1016/j.bbrc.2005.12.094
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Co-authors Med Uni Graz
Wolfsberger Stefan
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Abstract:
In a gene chip analysis of common pituitary tumor types, one of the genes with the most impressive tissue-specific expression regulation was delta-like 1 (DLK1), which was strongly expressed in GH-secreting (GH-S) pituitary tumors. In addition to pituitary adenomas, various endocrine tumors were subjected to real-time-quantitative PCR revealing high expression of DLK1 in normal pituitary tissue, in GH-S-, in one prolactin-secreting pituitary adenoma and in pheochromocytomas. Additionally, three DLK1 gene-derived subvariants were identified. The first, lacking 204 bp--coding for epidermal growth factor-like domain 6 and parts of the juxtamembrane region--was named Secredeltin. In the other two splice variants (named Brevideltin and Brevideltinin), a stop codon is introduced due to a frame-shift, leading to truncated proteins of 204 and 213 aas, respectively.
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Alternative Splicing - administration & dosage
Base Sequence - administration & dosage
Blotting, Northern - administration & dosage
Calcium-Binding Proteins - administration & dosage
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Codon, Terminator - administration & dosage
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Molecular Sequence Data - administration & dosage
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Polymerase Chain Reaction - administration & dosage
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Find related publications in this database (Keywords)
DLK1
pref-1
transcript variants
neuroendocrine tumors
pituitary adenomas
pituitary
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