Adrián Gonzalo
@adriangonzalo.bsky.social
200 followers 190 following 16 posts
Treasuring exceptions at IJPB (INRAE Versailles). Thirsty for genetics, chromosome biology and evolution.
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adriangonzalo.bsky.social
Sooooo well deserved!! Looking forward to learning all the new insights you will provide with your project😻
Reposted by Adrián Gonzalo
schnittger-lab.bsky.social
After 12 years…

In 2014, a wild idea was born: to follow female meiosis in Arabidopsis in real time. After many trials (including experiments with quirky mutants where female organs developed inside out, and a few other unconventional ideas), we switched gears to image the male side.
Reposted by Adrián Gonzalo
majdabohu.bsky.social
1/5 ✨Proud✨ to see our review with Katie Peichel as featured content in Trends_Ecol_Evo, with my beloved alpine lineages of Arabidopsis arenosa on the cover. Hope that you find it interesting! doi.org/10.1016/j.tree.2023.11.007
adriangonzalo.bsky.social
Check out the Views & News piece that Joiselle Fernandes and I wrote for @nature.com on the recent work from @amarques.bsky.social and colleagues about one of the most bizarre ways to do meiosis rdcu.be/euabu.

Explained for non-experts!
Diagram of two types of reproduction based on their meiosis. A. shows typical meiosis taking place in individuals with two copies of each chromosome (diploids) resulting in both male and female gametes carrying one copy of each chromosome. Fertilization restores the double copy for each chromosome. B. shows Canina meiosis in individuals carrying five copies of each chromosome (pentaploids) where male gametes only carry one copy of each chromosome and female gametes carry four copies of each chromosome. Fertilization restores the five copy for each chromosome.
adriangonzalo.bsky.social
Maybe holocentric chromosomes? Having centromeres dispersed all over the chromosome prevents loss of acentric fragments after breakage. Am I wrong, @amarques.bsky.social ?
adriangonzalo.bsky.social
Very interesting weirdo! Good job and congratulations!
adriangonzalo.bsky.social
En espagnol on dit "impulso meiótico" -> "impulsion méiotique"?
adriangonzalo.bsky.social
Finally, I must thank the other co-authors: Kirsten Bomblies and Aditya Nayak for their essential contributions to this work. It would have not been possible without them!
adriangonzalo.bsky.social
Conclusion: we found synapsis dynamics is severely compromised in neo-tetraploids, while in established ones it is more efficient even than diploids, and hybrids display sub-optimal synapsis. The extent of these synapsis defects is correlated with the degree of meiotic instability. 8/8.
A schematic timeline of synapsis completion using HEI10 dynamics as a “developmental clock”. In diploids, there is still some extensive asynapsis at the onset of HEI10 accumulation that quickly declines and synapsis completes as HEI10 accumulates. In neo-tetraploids there is extensive asynapsis, regardless of how advanced HEI10 accumulation is. In hybrids (cross between neo- and established tetraploid), the progression seems similar to that of diploids, but often fails to complete synapsis at the end of the process. Established tetraploids, show the most efficient dynamics, as very little asynapsis is left when HEI10 accumulation begins.
adriangonzalo.bsky.social
So, why is it so bad for NEO-4X to have incomplete synapsis? We don’t know but we observed certain (non-linear, probably complex) correlation between the extent of asynapsis and crossover number. Excess of crossovers, we know, is a problem for polyploid meiosis 7/8.
Plot of crossover number vs extent of asynapsis, R2 = 0.608, P < 0.0001
adriangonzalo.bsky.social
But why is synapsis so messed up in NEO-4X? We observed defects compatible with problems during earlier stages: less pre-synaptic co-alignments, and slower dynamics elongation of synapsis initiation sites. 6/8.
adriangonzalo.bsky.social
We modeled the initial extent of synapsis, the pace of synapsis completion, and the final extent of asynapsis. This suggested that NEO-4X synapsis progress stalls even before HE10 accumulation begins. In summary: EST-4X > 2X > > HYB-4X >>>>>> NEO-4X. 5/8.
Some examples of meiocytes with different degrees of synapsis completion and different levels of HEI10 accumulation. 
Plots showing comparisons between A. arenosa genotypes for the initial extent of synapsis, the pace of synapsis completion, and the final extent of asynapsis.
adriangonzalo.bsky.social
Are these defects associated with problems in synapsis progression? We used the dynamics of HEI10 as a “developmental clock”: many small foci at early stages, few bright foci in later stages, to measure how early/late is the completion of synapsis (measured by the disappearance of ASY1). 4/8
Using the level of HEI10 accumulation (what % of total signal accumulates at bright foci): The higher is the %, the later in the HEI10 dynamics we are. 
Using the length of ASY1 signal as a negative proxy for the degree of synapsis completion: The lower the ASY1 length, the closer to synapsis completeness. 
Plotting HEI10 accumulation level vs ASY1 length show the normal trend: the higher is the HEI10 accumulation level the lower is the ASY1 length. In other words: incomplete synapsis is associated to early stages of HEI10 accumulation, and vice versa; full synapsis is typical when HEI10 accumulation is high. HOWEVER, this is not the case for NEO-4X where there is no real progress of synapsis as HEI10 accumulates.
adriangonzalo.bsky.social
We analyzed this in Arabidopsis arenosa diploids (2X), newly induced tetraploids (NEO-4X), natural established tetraploids (EST-4X), and hybrids (EST-4X x NEO-4X), which have different levels of meiotic stability: 2X > EST-4X > HYB-4X >> NEO-4X. 3/8
Quantification of meiotic stability in NEO-4x, EST-4X and HYB-4X through the number of meiotic defects like quadrivalents (groups of four homologs associated by crossovers) and univalents (chromosomes that did not receive crossovers) in metaphase I. The frequency of these defects is correlated with the total number of crossovers (measured as the number of HEI10 foci).
adriangonzalo.bsky.social
Pairs of homologous chromosomes need to remain pair-wise associated during early meiosis thanks to the formation of the synaptonemal complex (synapsis) for a normal regulation of meiotic recombination, and fertility. But how messy can synapsis get in polyploids? Can polyploids solve this problem?2/8
adriangonzalo.bsky.social
Our latest work is out in @pnas.org! We have quantified and modeled the dynamics of early meiosis events, which can get really messy in polyploids (doubled number of chromosomes, double the trouble), but can also get fixed through adaptive evolution 🧵1/8.
www.pnas.org/doi/10.1073/...
Improved synapsis dynamics accompany meiotic stability in Arabidopsis arenosa autotetraploids | PNAS
During meiosis, the correct pairing, synapsis, and recombination of homologous chromosome pairs is critical for fertility of sexual eukaryotes. The...
www.pnas.org