The mouse type-III procollagen-encoding gene: genomic cloning and complete DNA sequence
Overlapping cosmid clones were isolated that covered the entire mouse type-III collagen-encoding gene (m Col3) locus including flanking sequences approximately 40 kb upstream and 20 kb downstream from the gene. This gene was characterized initially by restriction mapping and then followed by sequenc...
Gespeichert in:
Veröffentlicht in: | Gene 1994-09, Vol.147 (2), p.161-168 |
---|---|
Hauptverfasser: | , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
Zusammenfassung: | Overlapping cosmid clones were isolated that covered the entire mouse type-III collagen-encoding gene (m
Col3) locus including flanking sequences approximately 40 kb upstream and 20 kb downstream from the gene. This gene was characterized initially by restriction mapping and then followed by sequencing of 43.6 kb, including 5 kb upstream from the transcription start point (
tsp) and all exons and introns of the entire gene. The optimal parameters for sequencing a gene of this size were determined by sequencing 5–10-kb fragments at different ratios of random and directed sequencing, and comparing their efficiency. Based on our experience for sequencing m
Col3, we have estimated that the most cost-efficient method was to achieve a twofold redundancy in sequencing by using random DNA subclones as templates for sequencing prior to initiating directed DNA sequencing to close the gaps between contiguous regions. m
Col3 spans 37.6 kb from the
tsp to the single polyadenylation site and contains 51 exons. The overall structure of m
Col3 is similar to that of other members of the fibrillar collagen-encoding gene family. Several repetitive elements were located within the gene boundaries. Based on the nucleotide (nt) sequence, the predicted sizes of the mouse type-III collagen (mCOL3) mRNA and polypeptide are 4767 nt and 1464 amino acids (aa), respectively. A comparison of mCOL3 versus the human type-III collagen (hCOL3) showed 91% identity at the aa level. |
---|---|
ISSN: | 0378-1119 1879-0038 |
DOI: | 10.1016/0378-1119(94)90061-2 |