Islam Ahmed Abdulsahib Almsarrhad
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Research Subjects
Islam Ahmed Abdulsahib Almsarrhad has a total of 17 co-authors. Here are the top co-authors by number of shared publications:
- Balázs Kakuk
MTA-SZTE Lendület GeMiNI Research Group, University of Szeged, Somogyi st. 4., 6720 Szeged, Hungary
1 shared publication - Dóra Tombácz
Department of Medical Biology, Albert Szent-Györgyi Medical School, University of Szeged
1 shared publication - Gergely Ármin Nagy
Department of Medical Biology, Albert Szent-Györgyi Medical School, University of Szeged
1 shared publication - Gábor Gulyás
MTA-SZTE Lendület GeMiNI Research Group, University of Szeged, Somogyi st. 4., 6720 Szeged, Hungary
1 shared publication - Gábor Torma
Department of Medical Biology, Albert Szent-Györgyi Medical School, University of Szeged, Szeged, Hungary
1 shared publication - Ishaan Gupta
Department of Biochemical Engineering and Biotechnology, Indian Institute of Technology, New Delhi, India
1 shared publication
Latest Publications
- 10 September 2024
- Published by University of Szeged
Herpesvirus Transcriptomics as a Module of DNA Replication-Global Transcription Dynamics
- 10 September 2024
- Published by University of Szeged
Herpesvirus Transcriptomics as a Module of DNA Replication-Global Transcription Dynamics
- Open Access
Novel Herpesvirus Transcripts with Putative Regulatory Roles in DNA Replication and Global Transcription
In the last couple of years, the rapid advances and decreasing costs of sequencing technologies have revolutionized transcriptomic research. Long-read sequencing (LRS) techniques are able to detect full-length RNA molecules in a single run without the need for additional assembly steps. LRS studies have revealed an unexpected transcriptomic complexity in a variety of organisms, including viruses. A number of transcripts with proven or putative regulatory role, mapping close to or overlapping the replication origins (Oris) and the nearby transcription activator genes, have been described in herpesviruses. In this study, we applied both newly generated and previously published LRS and short-read sequencing datasets to discover additional Ori-proximal transcripts in nine herpesviruses belonging to all of the three subfamilies (alpha, beta and gamma). We identified novel long non-coding RNAs (lncRNAs), as well as splice and length isoforms of mRNAs and lncRNAs. Furthermore, our analysis disclosed an intricate meshwork of transcriptional overlaps at the examined genomic regions. Our results suggest the existence of a ‘super regulatory center’, which controls both the replication and the global transcription through multilevel interactions between the molecular machineries.
Open AccessNovel Herpesvirus Transcripts with Putative Regulatory Roles in DNA Replication and Global Transcription
In the last couple of years, the rapid advances and decreasing costs of sequencing technologies have revolutionized transcriptomic research. Long-read sequencing (LRS) techniques are able to detect full-length RNA molecules in a single run without the need for additional assembly steps. LRS studies have revealed an unexpected transcriptomic complexity in a variety of organisms, including viruses. A number of transcripts with proven or putative regulatory role, mapping close to or overlapping the replication origins (Oris) and the nearby transcription activator genes, have been described in herpesviruses. In this study, we applied both newly generated and previously published LRS and short-read sequencing datasets to discover additional Ori-proximal transcripts in nine herpesviruses belonging to all of the three subfamilies (alpha, beta and gamma). We identified novel long non-coding RNAs (lncRNAs), as well as splice and length isoforms of mRNAs and lncRNAs. Furthermore, our analysis disclosed an intricate meshwork of transcriptional overlaps at the examined genomic regions. Our results suggest the existence of a ‘super regulatory center’, which controls both the replication and the global transcription through multilevel interactions between the molecular machineries.