[bionet.molbio.genbank.updates] Human apolipoprotein A-I mRNA, complete cds.

GenBank-Updates@genbank.bio.net (02/28/91)

LOCUS       HUMAPOAIB     878 bp ss-mRNA            PRI       28-FEB-1991
DEFINITION  Human apolipoprotein A-I mRNA, complete cds.
ACCESSION   M27875
KEYWORDS    apolipoprotein; apolipoprotein A-I.
SOURCE      Human liver DNA, clone PNIV 1602.
  ORGANISM  Homo sapiens
            Eukaryota; Animalia; Metazoa; Chordata; Vertebrata; Mammalia;
            Theria; Eutheria; Primates; Haplorhini; Catarrhini; Hominidae.
REFERENCE   1  (sites)
  AUTHORS   Moguilevsky,N., Roobol,C., Loriau,R., Guillaume,J.P., Jacobs,P.,
            Cravador,A., Herzog,A., Brouwers,L., Scarso,A., Gilles,P.,
            Holmquist,L., Carlson,L.A. and Bollen,A.
  TITLE     Production of human recombinant proapolipoprotein A-I in
            Escherichia coli purification and biomedical characterization
  JOURNAL   DNA 8, 429-436 (1989)
  STANDARD  full staff_review
REFERENCE   2  (sites)
  AUTHORS   Funke,H., von Eckardstein,A., Pritchard,P.H., Karas,M., Albers,J.J.
            and Assmann,G.
  TITLE     A frameshift mutation in the human apolipoprotein A-1 gene causes
            high density lipoprotein dificiency, partial lecithin:
            Cholesterol-acyltransferase dificiency, and corneal opacities
  JOURNAL   J. Clin. Invest. 87, 371-376 (1991)
  STANDARD  full staff_review
COMMENT
            [DNA 8, 429-436 (1989)]  sites; for [Unpublished (1989) Rue de
            L'Industrie 24, B1400 Nivelles, Belgium].
            
            Draft entry and computer-readable sequence for [Unpublished (1989)
            Rue de L'Industrie 24, B1400 Nivelles, Belgium] kindly submitted
            by N.Moguilevsky, 13-OCT-1989.
FEATURES             Location/Qualifiers
     CDS             20..823
                     /note="proapolipoprotein /nomgen='APOA1' /map='11q23-q24'
                     /hgml_locus_uid='LE0096N'"
                     /codon_start=20
     sig_peptide     20..73
                     /note="apolipoprotein signal peptide"
                     /codon_start=20
     mat_peptide     92..820
                     /note="apolipoprotein"
                     /codon_start=92
     mutation        696..698
                     /note="cgc in wt; cc in mutation causing high density
                     lipoprotein deficiency."
                     /gene="APOA1"
                     /citation=J. Clin. Invest. 87, 371-376 (1991)
BASE COUNT      196 a    273 c    282 g    127 t
ORIGIN
        1 tcccccacgg cccttcagga tgaaagctgc ggtgctgacc ttggccgtgc tcttcctgac
       61 ggggagccag gctcggcatt tctggcagca agatgaaccc ccccagagcc cctgggatcg
      121 agtgaaggac ctggccactg tgtacgtgga tgtgctcaaa gacagcggca gagactatgt
      181 gtcccagttt gaaggctccg ccttgggaaa acagctaaac ctaaagctcc ttgacaactg
      241 ggacagcgtg acctccacct tcagcaagct gcgcgaacag ctcggccctg tgacccagga
      301 gttctgggat aacctggaaa aggagacaga gggcctgagg caggagatga gcaaggatct
      361 ggaggaggtg aaggccaagg tgcagcccta cctggacgac ttccagaaga agtggcagga
      421 ggagatggag ctctaccgcc agaaggtgga gccgctgcgc gcagagctcc aagagggcgc
      481 gcgccagaag ctgcacgagc tgcaagagaa gctgagccca ctgggcgagg agatgcgcga
      541 ccgcgcgcgc gcccatgtgg acgcgctgcg cacgcatctg gccccctaca gcgacgagct
      601 gcgccagcgc ttggccgcgc gccttgaggc tctcaaggag aacggcggcg ccagactggc
      661 cgagtaccac gccaaggcca ccgagcatct gagcacgctc agcgagaagg ccaagcccgc
      721 gctcgaggac ctccgccaag gcctgctgcc cgtgctggag agcttcaagg tcagcttcct
      781 gagcgctctc gaggagtaca ctaagaagct caacacccag tgaggcgccc gccgccgccc
      841 cccttcccgg tgctcagaat aaacgtttcc aaagtggg
//