Related Experiment Video
Updated: Nov 19, 2025

07:48
Use of Time-Lapse Microscopy and Stage-Specific Nuclear Depletion of Proteins to Study Meiosis in S. cerevisiae
Published on: October 11, 2022
2.1K
Barley Anther and Meiocyte Transcriptome Dynamics in Meiotic Prophase I
Abdellah Barakate1, Jamie Orr1, Miriam Schreiber1
1Cell and Molecular Sciences, The James Hutton Institute, Dundee, United Kingdom.
Frontiers in Plant Science
|January 29, 2021
Summary
Successful plant reproduction relies on precise gene regulation during meiosis. This study reveals key transcriptomic shifts and long non-coding RNA dynamics in barley anthers during meiosis entry, highlighting regulatory network complexity.
Area of Science:
- Plant reproductive biology
- Molecular genetics
- Transcriptomics
Background:
- Meiosis is crucial for sexual reproduction in flowering plants.
- Transcriptional regulation governs germ cell development and meiotic recombination.
- Environmental and genetic factors influence these processes.
Purpose of the Study:
- To investigate the temporal dynamics of gene expression during barley meiosis.
- To identify key transcriptional changes and regulatory elements involved in early meiotic stages.
- To understand the role of long non-coding RNAs in meiotic progression.
Main Methods:
- Short- and long-read RNA sequencing (RNA-seq) of immuno-cytologically staged barley anthers and meiocytes.
- Analysis of temporal transcript abundance dynamics from pre-meiosis through prophase I.
- Bioinformatic analysis to identify differentially expressed genes and long non-coding RNAs.
Main Results:
- Significant transcriptional reprogramming occurs at the transition from pre-meiosis to leptotene-zygotene.
- Pre-meiotic anthers show enrichment in long non-coding RNAs (lncRNAs), which are downregulated upon entry to meiosis.
- Transcript abundance remains relatively stable in meiocytes from prophase I to metaphase I-tetrad.
- A subset of meiotic gene orthologs (24%) exhibited differential expression.
- Specific proteins like Argonautes, E3 ubiquitin ligases, and de-ubiquitinating enzymes are enriched in prophase I meiocytes.
Conclusions:
- Meiosis entry in barley involves substantial transcriptomic reprogramming, particularly the downregulation of lncRNAs.
- Meiocyte transcriptomes are remarkably stable throughout prophase I after initial reprogramming.
- Complex regulatory networks involving specific protein families orchestrate early meiotic processes.
Related Concept Videos
Meiosis I
201.4K
Meiosis is a carefully orchestrated set of cell divisions, the goal of which—in humans—is to produce haploid sperm or eggs, each containing half the number of chromosomes present in somatic cells elsewhere in the body. Meiosis I is the first such division, and involves several key steps, among them: condensation of replicated chromosomes in diploid cells; the pairing of homologous chromosomes and their exchange of information; and finally, the separation of homologous chromosomes by...
201.4K
Meiosis I
43.2K
Meiosis is the division of a diploid cell into haploid cells forming sperm and eggs in animals through differentiation. Meiosis I is the first stage of meiosis, where the genetic recombination of homologous chromosomes and the reduction of the ploidy level by half occurs.
Prophase I is the most extended and complex step of meiosis I characterized by synapsis, chromosome pairing, and recombination of the homologous chromosomes. This process is facilitated by a proteinaceous structure called the...
Prophase I is the most extended and complex step of meiosis I characterized by synapsis, chromosome pairing, and recombination of the homologous chromosomes. This process is facilitated by a proteinaceous structure called the...
43.2K
Meiosis II
48.4K
Meiosis II entails cell division and segregation of the sister chromatids, resulting in the production of four unique haploid gametes. The steps for meiosis II are similar to mitosis, except that meiosis II occurs in haploid cells, whereas mitosis occurs in diploid cells.
The timing and cell division patterns of meiosis differ between males and females. In male meiosis, the centrosomes are part of the formation of the meiotic spindle. However, in oocytes, including that of humans, Drosophila,...
The timing and cell division patterns of meiosis differ between males and females. In male meiosis, the centrosomes are part of the formation of the meiotic spindle. However, in oocytes, including that of humans, Drosophila,...
48.4K
Meiosis II
190.8K
Meiosis II is the second and final stage of meiosis. It relies on the haploid cells produced during meiosis I, each of which contain only 23 chromosomes—one from each homologous initial pair. Importantly, each chromosome in these cells is composed of two joined copies, and when these cells enter meiosis II, the goal is to separate such sister chromatids using the same microtubule-based network employed in other division processes. The result of meiosis II is two haploid cells, each...
190.8K
Meiosis vs. Mitosis
65.3K
Cell division is necessary for growth and reproduction in organisms. Mitosis aids cell growth and development by dividing somatic cells. In contrast, meiosis causes the division of germ cells and plays an essential role in sexual reproduction. Due to their unique functional requirements, mitosis and meiosis differ from each other in multiple aspects.
Before the start of mitosis and meiosis I, the cell synthesizes DNA, resulting in two homologous copies of each chromosome. DNA synthesis is...
Before the start of mitosis and meiosis I, the cell synthesizes DNA, resulting in two homologous copies of each chromosome. DNA synthesis is...
65.3K
What is Meiosis?
233.1K
Meiosis is the process by which diploid cells divide to produce haploid daughter cells. In humans, each diploid cell contains 46 chromosomes, half from the mother and half from the father. Following meiosis, the resulting haploid eggs or sperm only contain 23 chromosomes; however, each of these chromosomes contains a unique combination of parental information that results from the meiotic process of crossing over.
233.1K

