Biology subjects

Guerrero, G.

Publications and source records attributed to Guerrero, G..

5 recordsLinked to original sources

bioRxiv2026

A putative cis-regulatory element near Shox2 in the jerboa genome (Jaculus jaculus) is not sufficient to alter mouse limb bone lengths

Vertebrate limb bones grow at different rates within and between species to achieve a striking variety of proportions and functions. However, most coding mutations that alter bone growth in mice and humans affect the entire skeleton, pointing to cis-regulatory modularity as the primary mechanism to diversify proportion. In a search for causative loci, we previously identified 1,755 disproportionately differentially expressed genes associated with the extreme hindlimb elongation in bipedal jerboas, Jaculus jaculus, compared to laboratory mice. We then took a focused approach to identify putative cis-regulatory elements near select candidate genes in a highly fragmented draft Jaculus jaculus genome assembly. We identified an ATAC-seq peak near Shox2 that was reproducible in jerboa metatarsals and not in radius/ulna. Shox2 gained a novel expression domain in jerboa metatarsals and is both necessary and sufficient to modulate mouse limb bone length. This 139 bp putative enhancer in the jerboa genome centers on a ~1 kb deletion of sequence found broadly throughout placental mammals. Here, we show that replicating the deletion and replacement with the 139 bp jerboa sequence in mice causes no detected phenotype. A genome-wide analysis of our ATAC-seq data using a high-quality Jaculus jaculus genome assembly replicated the peak called at this location but also identified 7,445 peaks that are similarly reproducible in metatarsals and not in radius/ulna. Certainly not all of these peaks are causative, but it is likely that many small-effect mutations diversified proportion. It is therefore crucial to apply unbiased filters to genome-wide analyses and to not assume that the few historically favored genes will have the largest effect.

evolutionary biology↗

bioRxiv2025

Expanding the fly eye gene regulatory network: from Drosophila to the hoverfly Episyrphus balteatus.

Comparing developmental mechanisms across long evolutionary distances is challenging, especially when the level of description in the compared species is very disparate. This is the case for the gene regulatory network (GRN) that underlies the development of compound eyes in insects, where the very detailed level description of the network in the fruit fly Drosophila melanogaster contrasts with the knowledge of the network in other well studied insects, such as the flour beetle Tribolium or the desert locust Schistocerca. It is not even known to what extent the Drosophila eye GRN is typical of flies (diptera). Here we have introduced the marmalade fly Episyrphus balteatus (Syrphidae), separated from Drosophila approximately 90 MYrs, as a fly species to compare the mechanisms of compound eye development. The Episyrphus eye develops from an imaginal disc which is, in the overall, similar to that of Drosophila. By generating parallel data sets in Episyrphus and Drosophila to maximize comparability, our results show how the genes known to participate in the early specification of the Drosophila eye and the onset of its differentiation are likely participating in the eye GRN of Episyrphus, further expanding the set of conserved genes/nodes in this network. This gene set might be the basis for further explorations of the developmental mechanisms involved in compound eye development beyond flies. By combining RNAseq and ATACseq profiling with TF motifs we derive the first eye GRN in Episyrphus. When built using Episyrphus/Drosophila conserved nodes, the resulting GRN model exhibited abundant internal connectivity, suggesting that, as proposed in Drosophila, the GRN is knitted with many regulatory feedbacks. Using link conservation as a criterion for discovering new regulatory interactions, we find that the AML1/Runx transcription factor lozenge (lz) is a negative regulator of the retinal determination gene dachshund (dac) in Drosophila. However, although many of the predicted regulatory links are conserved, a large number of regulatory connections seem species-specific, even among conserved nodes. This suggests quite a significant regulatory rewiring during the 90Myr period separating Episyrphus and Drosophila.

developmental biology↗

bioRxiv2022

Formation of sulfoquinovosyl diacylglycerol by acylation of sulfoquinovosyl glycerol

Sulfoquinovosyl diacylglycerol (SQDG) is a membrane-forming lipid present in photosynthetic organisms as well as in distinct bacteria growing in phosphate-limited environments. Four genes for SQDG biosynthesis were previously identified in Rhodobacter sphaeroides, the operon sqdBDC and sqdA. In this work, we found that SMc02490 of Sinorhizobium meliloti is an SqdA orthologue. Expression of the S. meliloti sqdBDC operon in Escherichia coli results in formation of sulfoquinovosyl glycerol (SQGro), while co-expression of this operon together with smc02490 (sqdA) results in formation of SQDG. Furthermore, SqdA allows for incorporation of exogenous SQGro into SQDG in S. meliloti and in E. coli cultures, suggesting that presence of SqdA in bacteria permit them to use environmental SQGro for the biosynthesis of the membrane lipid SQDG. An in vitro enzymatic assay for the acyltransferase SqdA was developed. Cell-free crude extracts of E. coli expressing sqdA can efficiently convert [35S]-sulfoquinovosyl monoacylglycerol into SQDG using as acyl donor acyl carrier protein. Bioinformatic analyses reveal that this sulfoquinovose acylation pathway for SQDG biosynthesis is delimited to the Hyphomicrobiales (Rhizobiales) and Rhodobacterales orders of Alphaproteobacteria.

microbiology↗

bioRxiv2021

Differences in orthodenticle expression promote ommatidial size variation between Drosophila species

The compound eyes of insects exhibit extensive variation in ommatidia number and size, which affects how they see and underlies adaptations in their vision to different environments and lifestyles. However, very little is known about the genetic and developmental bases of differences in compound eye size. We previously showed that the larger eyes of Drosophila mauritiana compared to D. simulans is generally caused by differences in ommatidia size rather than number. Furthermore, we identified an X-linked chromosomal region in D. mauritiana that results in larger eyes when introgressed into D. simulans. Here, we used a combination of fine-scale mapping and gene expression analysis to further investigate positional candidate genes on the X chromosome. We found earlier expression of orthodenticle (otd) during ommatidial maturation in third instar larvae in D. mauritiana than in D. simulans, and we show that this gene is required for the correct organisation and size of ommatidia in D. melanogaster. We discovered that the activity of an otd eye enhancer is consistent with the difference in the expression of this gene between species, with the D. mauritiana enhancer sequence driving earlier expression than that of D. simulans. We also identified potential direct targets of Otd that are differentially expressed between D. mauritiana and D. simulans during ommatidial maturation. Taken together, our results suggest that differential timing of otd expression contributes to natural variation in ommatidia size between D. mauritiana and D. simulans, which provides new insights into the mechanisms underlying the regulation and evolution of compound eye size in insects.

evolutionary biology↗

bioRxiv2019

In situ dissection of domain boundaries affect genome topology and gene transcription in Drosophila

The molecular mechanisms responsible for Topologically Associated Domains (TADs) formation are not yet fully understood. In Drosophila, it has been proposed that transcription is fundamental for TAD organization while the participation of genetic sequences bound by Architectural Proteins (APs) remains controversial. Here, we investigate the contribution of domain boundaries to TAD organization and the regulation of gene expression at the Notch gene locus in Drosophila. We find that deletion of domain boundaries results in TAD fusion and long-range topological defects that are accompanied by loss of APs and RNA Pol II chromatin binding as well as defects in transcription. Together, our results provide compelling evidence on the contribution of discrete genetic sequences bound by APs and RNA Pol II in the partition of the genome into TADs and in the regulation of gene expression in Drosophila.

genomics↗