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Molecular Cloning of a Novel cDNA From Mus Muscular BALB/c Mice Encoding Glycosyl Hydrolase Family 1: A Homolog of Human Lactase-Phlorizin Hydrolase 被引量:3

Molecular Cloning of a Novel cDNA From Mus Muscular BALB/c Mice Encoding Glycosyl Hydrolase Family 1: A Homolog of Human Lactase-Phlorizin Hydrolase
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摘要 Objective To study the mechanism of lactose intolerance (LI) by cloning the mouse lactase cDNA and recombining a vector. Methods Total murine RNA was isolated from the small intestine of a 4-week-old BALB/c mouse (δ). Crene-specific primers were designed and synthesized according to the cDNA sequences of lactase-phlorizin hydrolase (LPH) in human, rat, and rabbit. A coding sequence (CDS) fragment was obtained using RT-PCR, and inserted into a clone vector pNEB-193, then the cDNA was sequenced and analyzed using bioinformatics. Results The cDNA from the BALB/c mouse with 912 bp encoding 303 amino acid residues. Analysis of the deduced amino acid sequence using bioinforrnatics revealed that this cDNA shared extensive sequence homology with human LPH containing a conserved glycosyl hydrolase family 1 motif important for regulating lactase intolerance. Conclusion BALB/c mouse LPH cDNA (GenBank accession No: AY751548) provides a necessary foundation for study of the biological function and regulatory mechanism of the lactose intolerance in mice. Objective To study the mechanism of lactose intolerance (LI) by cloning the mouse lactase cDNA and recombining a vector. Methods Total murine RNA was isolated from the small intestine of a 4-week-old BALB/c mouse (δ). Crene-specific primers were designed and synthesized according to the cDNA sequences of lactase-phlorizin hydrolase (LPH) in human, rat, and rabbit. A coding sequence (CDS) fragment was obtained using RT-PCR, and inserted into a clone vector pNEB-193, then the cDNA was sequenced and analyzed using bioinformatics. Results The cDNA from the BALB/c mouse with 912 bp encoding 303 amino acid residues. Analysis of the deduced amino acid sequence using bioinforrnatics revealed that this cDNA shared extensive sequence homology with human LPH containing a conserved glycosyl hydrolase family 1 motif important for regulating lactase intolerance. Conclusion BALB/c mouse LPH cDNA (GenBank accession No: AY751548) provides a necessary foundation for study of the biological function and regulatory mechanism of the lactose intolerance in mice.
出处 《Biomedical and Environmental Sciences》 SCIE CAS CSCD 2006年第5期340-345,共6页 生物医学与环境科学(英文版)
基金 This work was supported by National Natural Science Foundation China (No. 30271126).
关键词 BALB/c mice LPH cDNA pNEB 193 Cloning Sequence BALB/c mice LPH cDNA pNEB 193 Cloning Sequence
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  • 1Swagerty D L Jr,Walling A D,Klein R M (2002).Lactose ntolerance.Am Fam Physician 65(9),1845-1850.
  • 2Auricchio S,Rubino A,Landolt M,et al.(1963).Isolated intestinal lactase deficiency in the adult.Lancet 2,324-326.
  • 3Dahlqvist A, Hammond J D, Grane R K, et al. (1963). Intestine lactase deficiency and lactose intolerance in adults: preliminary report. Gastroenterol 45, 488-491.
  • 4Sahi T, Isokoski M, Jussila J, et al, (1973). Recessive inheritance of adult-type iactose malabsorption. Lancet 2,823-826.
  • 5Sahi T (1994). Genetics and epidemiology of adult-type hypolactasia. Scand J Gastroenterol 29 (S 202), 7-20.
  • 6Potter J, Ho M-W, Bolten H, et al. (1985). Hurnan lactase and the molecular basis of lactase persistence Genet 23, 423-439.
  • 7Escher J C, de Koning N D, van Engen C G J,et al. (1992).Molecular basis of lactase levels in adult humans. J Clin Invest 89, 480-483.
  • 8Arola H, Tamm A (1994). Metabolism of lactose in the human body. Scand J Gastroenterol 29 (S 202), 21-25.
  • 9Burrin D G, Stoll B, Fan M Z, et al. (2001). Oral IGF-I alters the posttranslational processing but not the activity of lactase-phlorizin hydrolase in formula-fed neonatal pigs. J Nutr 131(9), 2235-2241.
  • 10Sambrook J, Fritsch E E Maniatis T (1989). MOLECULAR CLONING A Laboratory Manual, 2nd ed, Cold Spring Harbor Laboratory Press, 888-897.

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