Dieter Hackenberg
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Research Subjects
Research Interests
Dieter Hackenberg has a total of 9 co-authors. Here are the top co-authors by number of shared publications:
- Ann-Cathrin Lindner
Instituto Gulbenkian de Ciência, Oeiras, Portugal
2 shared publications - Božena Klodová
Institute of Experimental Botany of the Czech Academy of Sciences, Prague 6, Czech Republic
2 shared publications - Christos Michailidis
Laboratory of Pollen Biology, Institute of Experimental Botany of the Czech Academy of Sciences, Rozvojová 263, 165 00 Prague 6, Czech Republic
2 shared publications - David Honys
Laboratory of Pollen Biology, Institute of Experimental Botany of the Czech Academy of Sciences , Prague 6 165 00
2 shared publications - David Potěšil
Central European Institute of Technology, Masaryk University
2 shared publications - David Twell
Department of Genetics and Genome Biology, University of Leicester, Leicester, UK
2 shared publications
Latest Publications
- Open Access
- 15 June 2023
- Published by Springer Nature in Plant Reproduction
- Vol. 36 (3) , 285-286
Correction: Regulatory dynamics of gene expression in the developing male gametophyte of Arabidopsis
- 15 June 2023
- Published by Springer Nature in Plant Reproduction
- Vol. 36 (3) , 285-286
Open AccessCorrection: Regulatory dynamics of gene expression in the developing male gametophyte of Arabidopsis
- Open Access
- 25 October 2022
- Published by Springer Nature in Plant Reproduction
- Vol. 36 (3) , 213-241
Regulatory dynamics of gene expression in the developing male gametophyte of Arabidopsis
Sexual reproduction in angiosperms requires the production and delivery of two male gametes by a three-celled haploid male gametophyte. This demands synchronized gene expression in a short developmental window to ensure double fertilization and seed set. While transcriptomic changes in developing pollen are known for Arabidopsis, no studies have integrated RNA and proteomic data in this model. Further, the role of alternative splicing has not been fully addressed, yet post-transcriptional and post-translational regulation may have a key role in gene expression dynamics during microgametogenesis. We have refined and substantially updated global transcriptomic and proteomic changes in developing pollen for two Arabidopsis accessions. Despite the superiority of RNA-seq over microarray-based platforms, we demonstrate high reproducibility and comparability. We identify thousands of long non-coding RNAs as potential regulators of pollen development, hundreds of changes in alternative splicing and provide insight into mRNA translation rate and storage in developing pollen. Our analysis delivers an integrated perspective of gene expression dynamics in developing Arabidopsis pollen and a foundation for studying the role of alternative splicing in this model.
- 25 October 2022
- Published by Springer Nature in Plant Reproduction
- Vol. 36 (3) , 213-241
Open AccessRegulatory dynamics of gene expression in the developing male gametophyte of Arabidopsis
Sexual reproduction in angiosperms requires the production and delivery of two male gametes by a three-celled haploid male gametophyte. This demands synchronized gene expression in a short developmental window to ensure double fertilization and seed set. While transcriptomic changes in developing pollen are known for Arabidopsis, no studies have integrated RNA and proteomic data in this model. Further, the role of alternative splicing has not been fully addressed, yet post-transcriptional and post-translational regulation may have a key role in gene expression dynamics during microgametogenesis. We have refined and substantially updated global transcriptomic and proteomic changes in developing pollen for two Arabidopsis accessions. Despite the superiority of RNA-seq over microarray-based platforms, we demonstrate high reproducibility and comparability. We identify thousands of long non-coding RNAs as potential regulators of pollen development, hundreds of changes in alternative splicing and provide insight into mRNA translation rate and storage in developing pollen. Our analysis delivers an integrated perspective of gene expression dynamics in developing Arabidopsis pollen and a foundation for studying the role of alternative splicing in this model.