Literature DB >> 24190224

DNA fingerprinting analysis of Booroola pedigrees: a search for linkage to the Booroola gene.

A M Crawford1, P A Swarbrick, F C Buchanan, K G Dodds.   

Abstract

Seven minisatellite probes from a variety of sources were used to analyse 11 paternal half-sib families in which the Booroola gene was segregating. A total of 402 bands that showed segregation in the pedigrees were examined for linkage to the Booroola gene. None of the bands showed segregation with the Booroola gene. The most likely evidence for a linked band was produced by the HaRas HVR probe in Family 902 (θ=0.0; LOD 2.3). The conclusion, however, is that the minisatellite probes used in this study could not be used as markers for the Booroola gene. The study highlighted problems associated with the use of minisatellite probes in linkage studies in half-sib families. The complex banding patterns found on fingerprinting gels was a major source of scoring error. In a few cases both of the sire's alleles could be identified at a particular locus, but in most cases only one of the alleles could be identified. For the most part, the bands had to be treated as dominant alleles. The contribution of dam alleles to the banding pattern could only be estimated. There was an indication that minisatellite loci in sheep are clustered in particular regions of the sheep genome as the rate at which bands segregated with each other was higher than one would expect from loci randomly distributed throughout the genome.

Entities:  

Year:  1993        PMID: 24190224     DOI: 10.1007/BF00223776

Source DB:  PubMed          Journal:  Theor Appl Genet        ISSN: 0040-5752            Impact factor:   5.699


  23 in total

1.  Expression of the genes for alpha inhibin, beta A inhibin and follistatin in the ovaries of Booroola ewes which were homozygotes or non-carriers of the fecundity gene FecB.

Authors:  J S Fleming; D J Tisdall; P J Greenwood; N L Hudson; D A Heath; K P McNatty
Journal:  J Mol Endocrinol       Date:  1992-06       Impact factor: 5.098

2.  Repeat sequences from complex ds DNA viruses can be used as minisatellite probes for DNA fingerprinting.

Authors:  A M Crawford; F C Buchanan; K M Fraser; A J Robinson; D F Hill
Journal:  Anim Genet       Date:  1991       Impact factor: 3.169

3.  Chromosome morphology during meiosis of normal and Robertsonian translocation-carrying rams (Ovis aries).

Authors:  H M Chapman; A N Bruère
Journal:  Can J Genet Cytol       Date:  1977-03

4.  Simultaneous genetic mapping of multiple human minisatellite sequences using DNA fingerprinting.

Authors:  R A Wells; P Green; S T Reeders
Journal:  Genomics       Date:  1989-11       Impact factor: 5.736

5.  Differences in gonadotrophin concentrations and pituitary responsiveness to GnRH between Booroola ewes which were homozygous (FF), heterozygous (F+) and non-carriers (++) of a major gene influencing their ovulation rate.

Authors:  K P McNatty; N Hudson; K M Henderson; M Gibb; L Morrison; K Ball; P Smith
Journal:  J Reprod Fertil       Date:  1987-07

6.  Clustering of hypervariable minisatellites in the proterminal regions of human autosomes.

Authors:  N J Royle; R E Clarkson; Z Wong; A J Jeffreys
Journal:  Genomics       Date:  1988-11       Impact factor: 5.736

7.  Hypervariable 'minisatellite' regions in human DNA.

Authors:  A J Jeffreys; V Wilson; S L Thein
Journal:  Nature       Date:  1985 Mar 7-13       Impact factor: 49.962

8.  The highly polymorphic region near the human insulin gene is composed of simple tandemly repeating sequences.

Authors:  G I Bell; M J Selby; W J Rutter
Journal:  Nature       Date:  1982-01-07       Impact factor: 49.962

9.  A highly polymorphic locus in human DNA.

Authors:  A R Wyman; R White
Journal:  Proc Natl Acad Sci U S A       Date:  1980-11       Impact factor: 11.205

10.  On the use of DNA fingerprints for linkage studies in cattle.

Authors:  M Georges; M Lathrop; P Hilbert; A Marcotte; A Schwers; S Swillens; G Vassart; R Hanset
Journal:  Genomics       Date:  1990-03       Impact factor: 5.736

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