Literature DB >> 2837827

Tandem array of human visual pigment genes at Xq28.

D Vollrath1, J Nathans, R W Davis.   

Abstract

Unequal crossing-over within a head-to-tail tandem array of the homologous red and green visual pigment genes has been proposed to explain the observed variation in green-pigment gene number among individuals and the prevalence of red-green fusion genes among color-blind subjects. This model was tested by probing the structure of the red and green pigment loci with long-range physical mapping techniques. The loci were found to constitute a gene array with an approximately 39-kilobase repeat length. The position of the red pigment gene at the 5' edge of the array explains its lack of variation in copy number. Restriction maps of the array in four individuals who differ in gene number are consistent with a head-to-tail configuration of the genes. These results provide physical evidence in support of the model and help to explain the high incidence of color blindness in the human population.

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Year:  1988        PMID: 2837827     DOI: 10.1126/science.2837827

Source DB:  PubMed          Journal:  Science        ISSN: 0036-8075            Impact factor:   47.728


  53 in total

1.  Mutually exclusive expression of human red and green visual pigment-reporter transgenes occurs at high frequency in murine cone photoreceptors.

Authors:  Y Wang; P M Smallwood; M Cowan; D Blesh; A Lawler; J Nathans
Journal:  Proc Natl Acad Sci U S A       Date:  1999-04-27       Impact factor: 11.205

2.  Selective expression of human X chromosome-linked green opsin genes.

Authors:  J Winderickx; L Battisti; A G Motulsky; S S Deeb
Journal:  Proc Natl Acad Sci U S A       Date:  1992-10-15       Impact factor: 11.205

3.  Genotype-phenotype relationships in human red/green color-vision defects: molecular and psychophysical studies.

Authors:  S S Deeb; D T Lindsey; Y Hibiya; E Sanocki; J Winderickx; D Y Teller; A G Motulsky
Journal:  Am J Hum Genet       Date:  1992-10       Impact factor: 11.025

4.  Adrenoleucodystrophy: a molecular genetic study in five families.

Authors:  R G Del Mastro; S Bundey; M W Kilpatrick
Journal:  J Med Genet       Date:  1990-11       Impact factor: 6.318

5.  Structural genomic variation in ischemic stroke.

Authors:  Mar Matarin; Javier Simon-Sanchez; Hon-Chung Fung; Sonja Scholz; J Raphael Gibbs; Dena G Hernandez; Cynthia Crews; Angela Britton; Fabienne Wavrant De Vrieze; Thomas G Brott; Robert D Brown; Bradford B Worrall; Scott Silliman; L Douglas Case; John A Hardy; Stephen S Rich; James F Meschia; Andrew B Singleton
Journal:  Neurogenetics       Date:  2008-02-21       Impact factor: 2.660

6.  The L:M cone ratio in males of African descent with normal color vision.

Authors:  Carrie McMahon; Joseph Carroll; Stella Awua; Jay Neitz; Maureen Neitz
Journal:  J Vis       Date:  2008-02-20       Impact factor: 2.240

Review 7.  Potential genetic functions of tandem repeated DNA sequence blocks in the human genome are based on a highly conserved "chromatin folding code".

Authors:  P Vogt
Journal:  Hum Genet       Date:  1990-03       Impact factor: 4.132

8.  High-resolution microarray analysis unravels complex Xq28 aberrations in patients and carriers affected by X-linked blue cone monochromacy.

Authors:  S A Yatsenko; H A Bakos; K Vitullo; M Kedrov; A Kishore; B J Jennings; U Surti; M A Wood-Trageser; S Cercone; A N Yatsenko; A Rajkovic; A Iannaccone
Journal:  Clin Genet       Date:  2015-07-28       Impact factor: 4.438

Review 9.  New aspects of an old theme: the genetic basis of human color vision.

Authors:  B Wissinger; L T Sharpe
Journal:  Am J Hum Genet       Date:  1998-11       Impact factor: 11.025

10.  Molecular patterns and sequence polymorphisms in the red and green visual pigment genes of Japanese men.

Authors:  S S Deeb; A Alvarez; M Malkki; A G Motulsky
Journal:  Hum Genet       Date:  1995-05       Impact factor: 4.132

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