Abstract

Angiogenin (ANG) and ribonuclease 4 (RNASE4), two members of the secreted and vertebrate-specific ribonuclease superfamily, play important roles in cancers and neurodegenerative diseases. The ANG and RNASE4 genes share genetic regions with promoter activities, but the structure and regulation of these putative promotes are unknown. We have characterized the promoter regions, defined the transcription start site, and identified a mechanism of transcription regulation that involves both RNA polymerase III (Pol III) elements and CCCTC binding factor (CTCF) sites. We found that two Pol III elements within the promoter region influence ANG and RNASE4 expression in a position- and orientation-dependent manner. We also provide evidence for the presence of an intragenic chromatin loop between the two CTCF binding sites located in two introns flanking the ANG coding exon. We found that formation of this intragenic loop preferentially enhances ANG transcription. These results suggest a multilayer transcriptional regulation of ANG and RNASE4 gene locus. These data also add more direct evidence to the notion that Pol III elements are able to directly influence Pol II gene transcription. Furthermore, our data indicate that a CTCF-dependent chromatin loop is able to differentially regulate transcription of genes that share the same promoters.

Highlights

  • Angiogenin and ribonuclease 4 share genetic regions with promoter activities, and both have growth and survival activity

  • Our data indicate that the transcriptional activity of the ANG and ribonuclease 4 (RNASE4) promoter is influenced by RNA polymerase III (Pol III) elements and could be differentially regulated by an intragenic CCCTC binding factor (CTCF)-dependent chromatin loop

  • Chromatin State Segmentation of ANG and RNASE4 Gene Locus—The human ANG and RNASE4 genes are located on chromosome 14q11.2 and have a unique arrangement in which they share the same promoter regions and 5Ј-UTR followed by two distinct exons encoding the two proteins [23, 25]

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Summary

Background

Angiogenin and ribonuclease 4 share genetic regions with promoter activities, and both have growth and survival activity. In an attempt to understand the molecular mechanism by which ANG and RNASE4 transcription is regulated, we used bioinformatics analyses of the data sets released from the Encyclopedia of DNA Elements (ENCODE) project to discover functional elements in the ANG and RNASE4 locus These in silico-discovered elements were verified and defined experimentally by means of luciferase reporter, RNAi knockdown, and chromatin conformation capture (3-C) assays. Our data indicate that the transcriptional activity of the ANG and RNASE4 promoter is influenced by RNA polymerase III (Pol III) elements and could be differentially regulated by an intragenic CCCTC binding factor (CTCF)-dependent chromatin loop

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