Sequence and Chromosomal Context Effects on Variegated Expression of Keratin 5/lacZ Constructs in Stratified Epithelia of Transgenic Mice

Author:

Ramírez Angel1,Milot Eric2,Ponsa Immaculada3,Marcos-Gutiérrez Camelia4,Page Angustias1,Santos Mirentxu1,Jorcano José1,Vidal Miguel4

Affiliation:

1. Cell and Molecular Biology, Centro Investigaciones Medio Ambientales y Energeticas (CIEMAT), 28040 Madrid, Spain

2. Department of Cell Biology, Medical Genetics Center, Erasmus University, 3000 DR Rotterdam, The Netherlands

3. Departament de Biologia Cellular, Fisiologia i Immunologia, Facultat de Medicina, Universitat Autònoma de Barcelona, E-08193 Bellaterra, Spain

4. Department of Developmental and Cell Biology, Centro Investigaciones Biológicas, 28006 Madrid, Spain

Abstract

Abstract The expression of transgene loci in mammals often occurs in a heterocellular fashion resulting in variegated patterns of expression. We have examined the effect of chromosomal integration site, copy number, and transcriptionally activating sequences on the variegation of a keratin 5-lacZ (K5Z) construct in the stratified epithelia of transgenic mice. lacZ expression in these mice is always mosaic, and the β-gal activity per cell is usually higher in the lines with a higher proportion of expressing cells. Similar constructs, in which cDNAs were exchanged by lacZ sequences, showed no variegation. Also, when a strongly active, nonvariegating construct was coinjected with K5Z, most transgenic lines showed an almost homogeneous lacZ expression. The comparison of transgene arrays of different copies inserted at the same locus (obtained by using a lox/Cre system) showed that the reduction of copy number does not lead to an increase in the proportion of cells that express the transgene. Finally, in most of the variegating or nonexpressing lines the transgenes were located both at intermediate positions and at peritelomeric regions in the long chromosome arms. These findings suggest that the probability and efficiency of expression of K5Z genes depend on both long range chromosomal influences and on sequences in the transgene array.

Publisher

Oxford University Press (OUP)

Subject

Genetics

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