Literature DB >> 6623313

Lectin-resistant CHO cells: selection of new mutant phenotypes.

P Stanley.   

Abstract

Cytotoxic plant lectins select for mutants which exhibit unique structural changes in surface carbohydrates reflecting specific defects in glycosylation reactions. However, lectins are not highly specific selective agents and, as a result, only the most frequently occurring mutants are obtained from single lectin selections. We have previously shown that the specificity of lectin selections may be improved by utilizing a combination of lectins added together or sequentially. This strategy has now been further exploited in the search for novel lectin-resistant mutants of Chinese hamster ovary cells. Five new LecR phenotypes have been uncovered. One belongs to a new, recessive complementation group, two behave dominantly in somatic cell hybrids, and the remaining two appear to represent new phenotypes which fall into previously described complementation groups.

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Year:  1983        PMID: 6623313     DOI: 10.1007/bf01574260

Source DB:  PubMed          Journal:  Somatic Cell Genet        ISSN: 0098-0366


  21 in total

1.  "Stuck on sugars - how carbohydrates regulate cell adhesion, recognition, and signaling".

Authors:  Richard D Cummings
Journal:  Glycoconj J       Date:  2019-07-02       Impact factor: 2.916

2.  Chinese hamster ovary cell mutants with multiple glycosylation defects for production of glycoproteins with minimal carbohydrate heterogeneity.

Authors:  P Stanley
Journal:  Mol Cell Biol       Date:  1989-02       Impact factor: 4.272

3.  UDP-galactose (SLC35A2) and UDP-N-acetylglucosamine (SLC35A3) Transporters Form Glycosylation-related Complexes with Mannoside Acetylglucosaminyltransferases (Mgats).

Authors:  Dorota Maszczak-Seneczko; Paulina Sosicka; Beata Kaczmarek; Michał Majkowski; Marcin Luzarowski; Teresa Olczak; Mariusz Olczak
Journal:  J Biol Chem       Date:  2015-05-05       Impact factor: 5.157

4.  Transfection of a human gene that corrects the Lec1 glycosylation defect: evidence for transfer of the structural gene for N-acetylglucosaminyltransferase I.

Authors:  R Kumar; P Stanley
Journal:  Mol Cell Biol       Date:  1989-12       Impact factor: 4.272

5.  Biosynthesis of GlcNAc-rich N- and O-glycans in the Golgi apparatus does not require the nucleotide sugar transporter SLC35A3.

Authors:  Bozena Szulc; Paulina Sosicka; Dorota Maszczak-Seneczko; Edyta Skurska; Auhen Shauchuk; Teresa Olczak; Hudson H Freeze; Mariusz Olczak
Journal:  J Biol Chem       Date:  2020-09-16       Impact factor: 5.157

6.  Decreased tumorigenicity correlates with expression of altered cell surface carbohydrates in Lec9 CHO cells.

Authors:  J Ripka; S Shin; P Stanley
Journal:  Mol Cell Biol       Date:  1986-04       Impact factor: 4.272

7.  Control of carbohydrate processing: increased beta-1,6 branching in N-linked carbohydrates of Lec9 CHO mutants appears to arise from a defect in oligosaccharide-dolichol biosynthesis.

Authors:  A G Rosenwald; P Stanley; S S Krag
Journal:  Mol Cell Biol       Date:  1989-03       Impact factor: 4.272

8.  Membrane mutants of animal cells: rapid identification of those with a primary defect in glycosylation.

Authors:  P Stanley
Journal:  Mol Cell Biol       Date:  1985-05       Impact factor: 4.272

9.  UDP-N-acetylglucosamine transporter (SLC35A3) regulates biosynthesis of highly branched N-glycans and keratan sulfate.

Authors:  Dorota Maszczak-Seneczko; Paulina Sosicka; Teresa Olczak; Piotr Jakimowicz; Michał Majkowski; Mariusz Olczak
Journal:  J Biol Chem       Date:  2013-06-13       Impact factor: 5.157

10.  New liver cell mutants defective in the endocytic pathway.

Authors:  Richard J Stockert; Barry Potvin; Sangeeta Nath; Allan W Wolkoff; Pamela Stanley
Journal:  Biochim Biophys Acta       Date:  2007-04-14
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