Literature DB >> 7606932

Construction and characterization of a highly stable human: rodent monochromosomal hybrid panel for genetic complementation and genome mapping studies.

A P Cuthbert1, D A Trott, R M Ekong, S Jezzard, N L England, M Themis, C M Todd, R F Newbold.   

Abstract

Human:rodent somatic cell hybrids carrying a single, intact, selectable human chromosome are valuable both for functional somatic cell genetic analysis and genome mapping procedures. Here, we describe the construction and detailed molecular cytogenetic characterization of a panel of 23 stable hybrids, representing all 22 human autosomes plus the X-chromosome. Individual normal human chromosomes have been tagged with a selectable fusion gene (Hytk) introduced into the chromosome in a small (4.2 kbp) retroviral vector. Use of the Hytk marker permits both positive and negative ("in-out") selection to be applied to the human chromosome in any mammalian cell background. The panel includes 18 new hybrids isolated by direct microcell transfer from normal human diploid fibroblasts into mouse A9 cells.

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Year:  1995        PMID: 7606932     DOI: 10.1159/000134066

Source DB:  PubMed          Journal:  Cytogenet Cell Genet        ISSN: 0301-0171


  24 in total

1.  An activity associated with human chromosome 21 permits nuclear colocalization of the adenovirus E1B-55K and E4orf6 proteins and promotes viral late gene expression.

Authors:  Amy M Chastain-Moore; Terry Roberts; Deborah A Trott; Robert F Newbold; David A Ornelles
Journal:  J Virol       Date:  2003-07       Impact factor: 5.103

Review 2.  Insights into lysosomal cobalamin trafficking: lessons learned from cblF disease.

Authors:  Susann Gailus; Wolfgang Höhne; Bruno Gasnier; Peter Nürnberg; Brian Fowler; Frank Rutsch
Journal:  J Mol Med (Berl)       Date:  2010-02-20       Impact factor: 4.599

3.  RUNX1 permits E4orf6-directed nuclear localization of the adenovirus E1B-55K protein and associates with centers of viral DNA and RNA synthesis.

Authors:  Leslie J Marshall; Amy C Moore; Misao Ohki; Issay Kitabayashi; David Patterson; David A Ornelles
Journal:  J Virol       Date:  2008-04-16       Impact factor: 5.103

4.  Similar regions of human chromosome 3 are eliminated from or retained in human/human and human/mouse microcell hybrids during tumor growth in severe combined immunodeficient (SCID) mice.

Authors:  Y Yang; M Kost-Alimova; S Ingvarsson; Q Qianhui; H Kiss; A Szeles; I Kholodnyuk; A Cuthbert; G Klein; S Imreh
Journal:  Proc Natl Acad Sci U S A       Date:  2001-01-30       Impact factor: 11.205

5.  A novel syndrome affecting multiple mitochondrial functions, located by microcell-mediated transfer to chromosome 2p14-2p13.

Authors:  A Seyda; R F Newbold; T J Hudson; A Verner; N MacKay; S Winter; A Feigenbaum; S Malaney; D Gonzalez-Halphen; A P Cuthbert; B H Robinson
Journal:  Am J Hum Genet       Date:  2001-01-10       Impact factor: 11.025

6.  A mortality gene(s) for the human adenocarcinoma line HeLa maps to a 130-kb region of human chromosome 4q22-q23.

Authors:  Steven D Bryce; Vivienne Morrison; Nicola J Craig; Nicholas R Forsyth; Sara A Fitzsimmons; Hazel Ireland; Andrew P Cuthbert; Robert F Newbold; E Kenneth Parkinson
Journal:  Neoplasia       Date:  2002 Nov-Dec       Impact factor: 5.715

Review 7.  LMBRD1: the gene for the cblF defect of vitamin B₁₂ metabolism.

Authors:  Frank Rutsch; Susann Gailus; Terttu Suormala; Brian Fowler
Journal:  J Inherit Metab Dis       Date:  2010-05-06       Impact factor: 4.982

8.  Mutations in C12orf62, a factor that couples COX I synthesis with cytochrome c oxidase assembly, cause fatal neonatal lactic acidosis.

Authors:  Woranontee Weraarpachai; Florin Sasarman; Tamiko Nishimura; Hana Antonicka; Karine Auré; Agnès Rötig; Anne Lombès; Eric A Shoubridge
Journal:  Am J Hum Genet       Date:  2012-01-13       Impact factor: 11.025

Review 9.  The manipulation of chromosomes by mankind: the uses of microcell-mediated chromosome transfer.

Authors:  Karen J Meaburn; Christopher N Parris; Joanna M Bridger
Journal:  Chromosoma       Date:  2005-10-15       Impact factor: 4.316

10.  NDUFS6 mutations are a novel cause of lethal neonatal mitochondrial complex I deficiency.

Authors:  Denise M Kirby; Renato Salemi; Canny Sugiana; Akira Ohtake; Lee Parry; Katrina M Bell; Edwin P Kirk; Avihu Boneh; Robert W Taylor; Hans-Henrik M Dahl; Michael T Ryan; David R Thorburn
Journal:  J Clin Invest       Date:  2004-09       Impact factor: 14.808

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