Glycosylation Mutants of Mice and Animal Cells

Summary

Principal Investigator: PAMELA M STANLEY
Affiliation: Albert Einstein College of Medicine
Country: USA
Abstract: [unreadable] DESCRIPTION (provided by applicant): The long term goal of this project is to identify biological roles for mammalian glycans in development and cancer. Glycosyltransferase gene mutants of mice, embryonic stem (ES) cells and CHO cells will be used to investigate the basis of cell-type specific blocks to differentiation and transformation caused by alterations in specific glycans. Our recent studies show that 1) oocyte-specific knockout of complex and hybrid N-glycans compromises ovulation and oocyte developmental competence, but fertilization, blastogenesis and implantation proceed in the absence of these glycans; 2) the bisecting GlcNAc on complex N-glycans of non-hepatocyte glycoprotein(s) promotes hepatocarcinogenesis and liver regeneration after partial hepatectomy; and 3) deletion of mouse protein O-fucosyltransferase 1 generates a canonical Notch signaling phenotype identifying the Pofut1 gene as an essential component of the Notch signaling pathway. We now propose in Specific Aim 1 to investigate the molecular basis of the requirement for complex and hybrid N-glycans in oogenesis, and to identify roles of mucin O-glycans and O-fucose glycans in early development after oocyte-specific deletion of the core 1 beta3GalT-1 (C1galt1) or Pofut1 genes. In Specific Aim 2 the hypothesis that a triantennary, GlcNAc-terminating complex N- glycan is required for spermatogenesis will be investigated by deletion of a novel GlcNAc-transferase gene that is expressed almost exclusively in testis and by eliminating complex and hybrid N-glycans from spermatocytes, spermatogonia or Sertoli cells. The Pofut1 gene will also be deleted in spermatocytes and spermatogonia or Sertoli cells to identify roles for Notch signaling in spermatogenesis. In Specific Aim 3 the hypothesis that the Mgat3 gene may function as a tumor suppressor in mammary gland will be tested in the MMTV-Polyoma middle T (PyMT) mammary tumor model which metastasizes to lung and in cell signaling assays. In addition, roles for N- and 0-fucose glycans and Notch signaling will be investigated in mammary gland development and transformation by selective deletion of the Mgat1 and Pofut1 genes in mammary epithelia before puberty using MMTVCre, or during pregnancy using whey acidic protein (WAP) Cre recombinase. [unreadable] [unreadable]
Funding Period: 1981-08-01 - 2010-11-30
more information: NIH RePORT

Top Publications

  1. pmc Mouse fertility is enhanced by oocyte-specific loss of core 1-derived O-glycans
    Suzannah A Williams
    Department of Cell Biology, Albert Einstein College of Medicine, New York, New York 10461, USA
    FASEB J 22:2273-84. 2008
  2. pmc Bisected, complex N-glycans and galectins in mouse mammary tumor progression and human breast cancer
    Hazuki E Miwa
    Department of Cell Biology
    Glycobiology 23:1477-90. 2013
  3. pmc Complex N-glycans or core 1-derived O-glycans are not required for the expression of stage-specific antigens SSEA-1, SSEA-3, SSEA-4, or Le(Y) in the preimplantation mouse embryo
    Suzannah A Williams
    Department of Cell Biology, Albert Einstein College of Medicine, New York, NY 10461, USA
    Glycoconj J 26:335-47. 2009
  4. pmc The bisecting GlcNAc on N-glycans inhibits growth factor signaling and retards mammary tumor progression
    Yinghui Song
    Department of Cell Biology, Albert Einstein College of Medicine of Yeshiva University, Bronx, New York 10461, USA
    Cancer Res 70:3361-71. 2010
  5. pmc Complex N-glycans are essential, but core 1 and 2 mucin O-glycans, O-fucose glycans, and NOTCH1 are dispensable, for mammalian spermatogenesis
    Frank Batista
    Department of Cell Biology, Albert Einstein College Medicine, New York, New York, USA
    Biol Reprod 86:179. 2012
  6. ncbi Suppressors of alpha(1,3)fucosylation identified by expression cloning in the LEC11B gain-of-function CHO mutant
    Wei Chen
    Department of Cell Biology, Albert Einstein College of Medicine, New York, NY 10461, USA
    Glycobiology 15:259-69. 2005
  7. ncbi Fertilization in mouse does not require terminal galactose or N-acetylglucosamine on the zona pellucida glycans
    Suzannah A Williams
    Department of Cell Biology, Albert Einstein College of Medicine, New York, NY 10461, USA
    J Cell Sci 120:1341-9. 2007
  8. pmc Oocyte-specific deletion of complex and hybrid N-glycans leads to defects in preovulatory follicle and cumulus mass development
    Suzannah A Williams
    Department of Cell Biology, Albert Einstein College of Medicine, New York, New York 10461, USA
    Reproduction 137:321-31. 2009

Detail Information

Publications8

  1. pmc Mouse fertility is enhanced by oocyte-specific loss of core 1-derived O-glycans
    Suzannah A Williams
    Department of Cell Biology, Albert Einstein College of Medicine, New York, New York 10461, USA
    FASEB J 22:2273-84. 2008
    ..These results identify novel roles for glycoproteins from the oocyte as suppressors of fertility and regulators of follicular integrity in the mouse...
  2. pmc Bisected, complex N-glycans and galectins in mouse mammary tumor progression and human breast cancer
    Hazuki E Miwa
    Department of Cell Biology
    Glycobiology 23:1477-90. 2013
    ....
  3. pmc Complex N-glycans or core 1-derived O-glycans are not required for the expression of stage-specific antigens SSEA-1, SSEA-3, SSEA-4, or Le(Y) in the preimplantation mouse embryo
    Suzannah A Williams
    Department of Cell Biology, Albert Einstein College of Medicine, New York, NY 10461, USA
    Glycoconj J 26:335-47. 2009
    ..Furthermore, neither of these classes of glycan is essential for the expression of SSEA-1, SSEA-3, SSEA-4 or Le(Y) on mouse embryos...
  4. pmc The bisecting GlcNAc on N-glycans inhibits growth factor signaling and retards mammary tumor progression
    Yinghui Song
    Department of Cell Biology, Albert Einstein College of Medicine of Yeshiva University, Bronx, New York 10461, USA
    Cancer Res 70:3361-71. 2010
    ..Thus, the addition of the bisecting GlcNAc to complex N-glycans of mammary tumor cell glycoprotein receptors is a cell autonomous mechanism serving to retard tumor progression by reducing growth factor signaling...
  5. pmc Complex N-glycans are essential, but core 1 and 2 mucin O-glycans, O-fucose glycans, and NOTCH1 are dispensable, for mammalian spermatogenesis
    Frank Batista
    Department of Cell Biology, Albert Einstein College Medicine, New York, New York, USA
    Biol Reprod 86:179. 2012
    ..Therefore, although core 1 and 2 mucin O-glycans, NOTCH1, POFUT1, O-fucose glycans, and Notch signaling are dispensable, MGAT1 and complex N-glycans are essential for spermatogenesis...
  6. ncbi Suppressors of alpha(1,3)fucosylation identified by expression cloning in the LEC11B gain-of-function CHO mutant
    Wei Chen
    Department of Cell Biology, Albert Einstein College of Medicine, New York, NY 10461, USA
    Glycobiology 15:259-69. 2005
    ....
  7. ncbi Fertilization in mouse does not require terminal galactose or N-acetylglucosamine on the zona pellucida glycans
    Suzannah A Williams
    Department of Cell Biology, Albert Einstein College of Medicine, New York, NY 10461, USA
    J Cell Sci 120:1341-9. 2007
    ..The combined data show that mouse ZP3 does not require terminal Gal or GlcNAc on either N- or O-glycans for fertilization...
  8. pmc Oocyte-specific deletion of complex and hybrid N-glycans leads to defects in preovulatory follicle and cumulus mass development
    Suzannah A Williams
    Department of Cell Biology, Albert Einstein College of Medicine, New York, New York 10461, USA
    Reproduction 137:321-31. 2009
    ..Therefore, the absence of complex and hybrid N-glycans on oocyte glycoproteins leads to abnormal folliculogenesis resulting in a decreased ovulation rate...