Literature DB >> 6930703

Marker segregation without chromosome loss at the emt locus in Chinese hamster cell hybrids.

R G Worton, C Duff, C E Campbell.   

Abstract

Segregation, defined as the reexpression of the recessive phenotype, has been examined in Chinese hamster cell hybrids heterozygous at the recessive emtr locus. Segregants were selected in emetine, and the role of chromosome loss in the segregation process was evaluated by detailed karyotype comparison of segregants with their hybrid parent. In emtr CHO x emt+ CHO hybrids (CHO is thought to be hemizygous at the emt locus), segregants were obtained at high frequency, and no consistent chromosome loss was found in the segregants. In hybrids made with Emtr CHO and wild-type lines other than CHO (CHW,CHL,V-79), where two wild-type alleles are thought to be present in the hybrid, segregants were obtained at much lower frequency, consistent with a two-step segregation process. These segregants revealed consistent loss of one chromosome 2 or deletion of a part of the long arm of a chromosome 2. Thus, one step in segregation seems to be chromosome loss while the other step must have a different mechanism, possibly the same mechanism that operates in the CHO x CHO hybrids. Two major conclusions can be drawn: (1) the emt gene maps to a hemizygous region of the long arm of a chromosome 2 in Chinese hamster, and (2) a segregation mechanism other than chromosome loss appears to operate with high efficiency in intraspecific hybrids.

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Year:  1980        PMID: 6930703     DOI: 10.1007/bf01538796

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


  12 in total

1.  Gene inactivation as a mechanism for the expression of recessive phenotypes.

Authors:  S G Grant; C E Campbell; C Duff; S L Toth; R G Worton
Journal:  Am J Hum Genet       Date:  1989-10       Impact factor: 11.025

2.  Densely methylated DNA islands in mammalian chromosomal replication origins.

Authors:  E S Tasheva; D J Roufa
Journal:  Mol Cell Biol       Date:  1994-09       Impact factor: 4.272

3.  Microcell-mediated cotransfer of genes specifying methotrexate resistance, emetine sensitivity, and chromate sensitivity with Chinese hamster chromosome 2.

Authors:  R Worton; C Duff; W Flintoff
Journal:  Mol Cell Biol       Date:  1981-04       Impact factor: 4.272

4.  Identification and characterization of a third complementation group of emetine-resistant Chinese hamster cell mutants.

Authors:  J J Wasmuth; J M Hill; L S Vock
Journal:  Mol Cell Biol       Date:  1981-01       Impact factor: 4.272

5.  Chemical carcinogens transform BHK cells by inducing a recessive mutation.

Authors:  N Bouck; G di Mayorca
Journal:  Mol Cell Biol       Date:  1982-02       Impact factor: 4.272

6.  Genetic and biochemical distinction among Chinese hamster cell emtA, emtB, and emtC mutants.

Authors:  S Chang; J J Wasmuth
Journal:  Mol Cell Biol       Date:  1983-03       Impact factor: 4.272

7.  Primary structure of human ribosomal protein S14 and the gene that encodes it.

Authors:  D D Rhoads; A Dixit; D J Roufa
Journal:  Mol Cell Biol       Date:  1986-08       Impact factor: 4.272

8.  Spontaneous fusion in vivo between normal host and tumor cells: possible contribution to tumor progression and metastasis studied with a lectin-resistant mutant tumor.

Authors:  R S Kerbel; A E Lagarde; J W Dennis; T P Donaghue
Journal:  Mol Cell Biol       Date:  1983-04       Impact factor: 4.272

9.  Ribosomal protein S14 is altered by two-step emetine resistance mutations in Chinese hamster cells.

Authors:  J J Madjar; M Frahm; S McGill; D J Roufa
Journal:  Mol Cell Biol       Date:  1983-02       Impact factor: 4.272

10.  Chromosome segregation is frequently associated with the expression of recessive mutations in mouse cells.

Authors:  E M Eves; R A Farber
Journal:  Proc Natl Acad Sci U S A       Date:  1981-03       Impact factor: 11.205

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