Abstract
The complete (17159 bp) nucleotide sequence of the gene for the human C1 inhibitor has been determined. The transcription initiation site was examined by primer extension using human liver mRNA, and the messenger 5′‐end sequence was determined on clones obtained by the anchored polymerase chain reaction. The gene of this serpin molecule is split by seven introns, with junctions of phases zero and one. An outstanding feature of the intron sequences is the occurrence of 17 AluI repeats of all four ancestral subgroups, indicating that the gene has been invaded during consecutive waves of Alu amplification, including a recent one. These Alu repeats form the sites of deletion and insertion in several known lesions in the C1‐inhibitor gene. There is no obvious promoter site of the TATA‐box type at the 5′ end of the gene, but instead it contains a region of potential H‐DNA structure similar to that found upstream of the human c‐myc gene.
Original language | English |
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Pages (from-to) | 301-308 |
Number of pages | 8 |
Journal | European Journal of Biochemistry |
Volume | 197 |
Issue number | 2 |
DOIs | |
Publication status | Published - 1 Jan 1991 |
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Human mRNA fragment for neurone-specific enolase
Fothergill, J. E. (Creator) & Paton, G. (Data Manager), GenBank, 1988
https://www.ncbi.nlm.nih.gov/nucleotide/X13120
Dataset
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Human gene for C1-inhibitor
Fothergill, J. E. (Creator) & Paton, G. (Data Manager), GenBank, 1990
https://www.ncbi.nlm.nih.gov/nucleotide/X54486
Dataset