Complete nucleotide sequence of ovine β-casein cDNA: inter-species comparison

The complete nucleotide sequence of ovine β-casein mRNA has been determined by sequencing, according to Sanger-Messing, both a recombinant clone isolated from a mammary cDNA pUC 18 library and a single-stranded cDNA generated by reverse transcription from a synthetic 17-mer primer complementary to t...

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Bibliographic Details
Published inBiochimie Vol. 71; no. 7; pp. 827 - 832
Main Authors Provot, Christian, Persuy, Marie-Annick, Mercier, Jean-Claude
Format Journal Article
LanguageEnglish
Published Paris Elsevier Masson SAS 01.07.1989
Elsevier
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Summary:The complete nucleotide sequence of ovine β-casein mRNA has been determined by sequencing, according to Sanger-Messing, both a recombinant clone isolated from a mammary cDNA pUC 18 library and a single-stranded cDNA generated by reverse transcription from a synthetic 17-mer primer complementary to the 5′ part of the mRNA coding frame. The 1088 nucleotide long β-casein mRNA, excluding the poly(A) tail, contains a coding frame of 669 nucleotides including the stop codon, flanked by 60 adn 359 nucleotides in the 5′ and 3′ untranslated regions, respectively. It arises from the splicing of 9 exons as deduced from gene sequence data. The deduced amino acid sequence differs at 3 positions from that previously determined by direct sequencing of mature β-casein. Comparison of the ovine, bovine, rat, mouse, and rabbit β-casein mRNA sequences shows a higher homology in the 3′ and 5′ untranslated regions. The most conserved regions in the open reading frame are essentially those encoding the signal peptide and the major phosphorylation site.
Bibliography:8905907
Q04
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ISSN:0300-9084
1638-6183
DOI:10.1016/0300-9084(89)90046-1