UDP-galactose: β-
A novel gene defining a novel enzyme in the UDP-D-galactose: beta-N-acetylglucosamine/beta-N-acetylgalactosamine beta 1,3galactosyltransferase family, termed beta3Gal-T5, with unique enzymatic properties is disclosed. The enzymatic activity of beta3Gal-T5 is shown to be distinct from that of previously identified enzymes of this gene family. The invention discloses isolated DNA molecules and DNA constructs encoding beta3Gal-T5 and derivatives thereof by way of amino acid deletion, substitution or insertion exhibiting beta3Gal-T5 activity, as well as cloning and expression vectors including such DNA, cells transfected with the vectors, and recombinant methods for providing beta3Gal-T5. The enzyme beta3Gal-T5 and beta3Gal-T5-active derivatives thereof are disclosed, in particular soluble derivatives comprising the catalytically active domain of beta3Gal-T5. Further, the invention discloses methods of obtaining beta 1,3galactosyl glycosylated saccharides, glycopeptides or glycoproteins by use of an enzymically active beta3Gal-T5 protein or fusion protein thereof or by using cells stably transfected with a vector including DNA encoding an enzymatically active beta3Gal-T5 protein as an expression system for recombinant production of such glycopeptides or glycoproteins. Also a method for the identification of DNA sequence variations in the beta3Gal-T5 gene by isolating DNA from a patient, amplifying beta3Gal-T5-coding exons by PCR, and detecting the presence of DNA sequence variation, are disclosed.
1. An isolated nucleic acid probe of less than 10,000 contiguous nucleotides, wherein the probe hybridizes with the entire length of a second nucleic acid comprising:
nucleotides 1-115 of SEQ ID NO:8; and
wherein the hybridization conditions comprise:
i. overnight incubation at 42° C. of a nucleic acid blot with the probe;
ii. washing of the blot at room temperature with 0.5×SSC and 1% Na 4 P 2 O 2 ;
iii. washing of the blot at 65° C. with 0.2×SSC, 1% SDS, and 1% Na 4 P 2 O 2; and
iv. washing of the blot with 0.2×SSC at room temperature, and wherein said probe hybridizes to a polynucleotide encoding a β3Gal-T5 and not to polynucleotides encoding β3Gal-T1, β3Gal-T2, β3Gal-T3, or β3Gal-T4 family members.
2. A complement of the isolated nucleic acid probe of claim 1 .
3. An isolated nucleic acid probe of less than 10,000 contiguous nucleotides, wherein the probe hybridizes with the entire length of a second nucleic acid comprising 428-1011 of SEQ ID NO:8; and the hybridization conditions comprise:
i. overnight incubation at 42° C. of a nucleic acid blot with the probe;
ii. washing of the blot at room temperature with 2×SSC and 1% Na 4 P 2 O 2 ;
iii. washing of the blot at 65° C. with 0.2×SSC, 1% SDS, and 1% Na 4 P 2 O 2; and
iv. washing of the blot with 0.2×SSC at room temperature, and wherein said probe hybridizes to a polynucleotide encoding a β3Gal-T5 and not to polynucleotides encoding β3Gal-T1, β3Gal-T2, β3Gal-T3, or β3Gal-T4 family members.
4. A complement of the isolated nucleic acid probe of claim 3 .