Abstract

BackgroundAn uncharacterized histone H2a-coding transcript (E130307C13) has been cloned from a mouse full-length cDNA library. This transcript is encoded on chromosome 6, approximately 4 kb upstream of a histone H4 gene, Hist4h4. The proteins encoded by this transcript and the human H2afj mRNA isoform-2 have the highest amino acid similarity. In this paper, we characterize it from the expression pattern given by quantitative RT-PCR.ResultsQuantitative RT-PCR indicated that the gene that encodes E130307C13 (E130307C13) is regulated in a replication-independent manner, and therefore it is H2afj. Certainly, H2afj transcript lacks a stem-loop structure at the 3'-UTR but contains a poly (A) signal. In addition, its promoter region has a different structure from those of the replication-dependent histone H2a genes.ConclusionThe bioinformatics imply that E130307C13 is a replication-independent H2a gene. In addition, quantitative RT-PCR analysis shows that it is replication-independent. Thus, it is H2afj, a novel replication-independent H2a gene in mouse.

Highlights

  • An uncharacterized histone H2a-coding transcript (E130307C13) has been cloned from a mouse full-length cDNA library

  • Replication of the eukaryotic chromosomes requires the synthesis of histones to package the newly replicated DNA into chromatin

  • E130307C13 lies on chromosome 6, approximately 4 kb upstream of Hist4h4. We characterize it from the expression pattern given by quantitative RT-PCR

Read more

Summary

Results

Quantitative RT-PCR indicated that the gene that encodes E130307C13 (E130307C13) is regulated in a replication-independent manner, and it is H2afj. H2afj transcript lacks a stem-loop structure at the 3'-UTR but contains a poly (A) signal. Its promoter region has a different structure from those of the replication-dependent histone H2a genes

Background
Results and discussion
Methods
Osley MA
Full Text
Paper version not known

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.