Transcription-dependent spatial arrangements of CFTR and adjacent genes in human cell nuclei

Author:

Zink Daniele1,Amaral Margarida D.23,Englmann Andreas1,Lang Susanne1,Clarke Luka A.2,Rudolph Carsten4,Alt Felix1,Luther Kathrin1,Braz Carla2,Sadoni Nicolas1,Rosenecker Joseph4,Schindelhauer Dirk56

Affiliation:

1. Ludwig Maximilians University Munich, Department of Biology II, 80336 Munich, Germany

2. Department of Chemistry and Biochemistry, Faculty of Sciences, University of Lisboa, 1749-016 Lisboa, Portugal

3. Center of Human Genetics, National Institute of Health, 1649-016 Lisboa, Portugal

4. Ludwig Maximilians University Munich, Division of Molecular Pulmonology, Department of Pediatrics, 80337 Munich, Germany

5. Technical University of Munich, Institute of Human Genetics, 81675 Munich, Germany

6. Life Science Center Weihenstephan, 85354 Freising, Germany

Abstract

We investigated in different human cell types nuclear positioning and transcriptional regulation of the functionally unrelated genes GASZ, CFTR, and CORTBP2, mapping to adjacent loci on human chromosome 7q31. When inactive, GASZ, CFTR, and CORTBP2 preferentially associated with the nuclear periphery and with perinuclear heterochromatin, whereas in their actively transcribed states the gene loci preferentially associated with euchromatin in the nuclear interior. Adjacent genes associated simultaneously with these distinct chromatin fractions localizing at different nuclear regions, in accordance with their individual transcriptional regulation. Although the nuclear localization of CFTR changed after altering its transcription levels, the transcriptional status of CFTR was not changed by driving this gene into a different nuclear environment. This implied that the transcriptional activity affected the nuclear positioning, and not vice versa. Together, the results show that small chromosomal subregions can display highly flexible nuclear organizations that are regulated at the level of individual genes in a transcription-dependent manner.

Publisher

Rockefeller University Press

Subject

Cell Biology

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