Biology subjects

Pask, A. J.

Publications and source records attributed to Pask, A. J..

13 recordsLinked to original sources

bioRxiv2026

Genomes of two arid-zone marsupials uncover contrasting responses to climatic change

Small marsupials in the family Dasyuridae are a key component of Australias arid and semi-arid fauna, whose high species richness is proposed to reflect an opportunity-driven adaptive radiation. Despite growing interest in this group from both ecological and evolutionary perspectives, genomic data for most species is non-existent, or limited to a few marker loci. Here, we generated a chromosome-level reference genome and a de novo mitochondrial genome for the desert-dwelling Wongai ningaui (Ningaui ridei). The nuclear genome assembly is highly contiguous, with a scaffold N50 of 594.5 MB and high BUSCO gene recovery (93.8%). Additionally, we produced a draft assembly for the related, semi-arid slender-tailed dunnart (Sminthopsis murina). We then used these assemblies to explore the demographic histories of these species. We find evidence for contrasting patterns of population growth during the late Pleistocene and early Holocene, corresponding with differences in local climate, potentially consistent with differences in optimal habitat. The new genomic resources and demographic findings presented here provide a foundation for future studies on adaptive specialisation in this group of Australian marsupials. Significance StatementDasyurid marsupials are the primary carnivorous and insectivorous mammals in Australia. This family includes species such as the endangered Tasmanian devil (Sarcophilus harrisii) and quolls (Genus Dasyurus), as well as an emerging model species, the fat-tailed dunnart (Sminthopsis crassicaudata). Despite the species richness within dasyurids, most species remain under-studied. This is particularly true of arid and semi-arid zone species, who are often small in size, live in remote habitats and are cryptic by nature. By creating genome assemblies for two dasyurid species, this study provides resources to support phylogenetic, comparative and conservation research in arid zone marsupials. Importantly, the studys finding that arid and semi-arid species show distinct trajectories of demographic change in response to historical climate may have implications for the resilience of locally-adapted dasyurid species to ongoing climate change.

genomics↗

bioRxiv2025

Getting a head start: Craniofacial heterochrony in marsupials involves dynamic changes to molecular and cellular mechanisms underlying neural crest development

The neural crest is a vertebrate innovation central to craniofacial development and evolution. While the gene regulatory networks guiding neural crest development are well characterized, the mechanisms generating species-specific craniofacial diversity remain poorly understood. Marsupials provide a unique model for studying neural crest plasticity, having evolved accelerated patterns of craniofacial development during embryogenesis. This adaptation arises in response to marsupials being born altricial after a short gestation yet require well-developed mouthparts to attach to a teat and continue development in the pouch. However, how marsupials achieve this heterochronic shift in neural crest development is largely unknown. In this study, we investigate the cellular and molecular mechanisms underlying their distinct heterochrony, revealing that marsupials produce dense pre-migratory aggregates of neural crest cells which undergo collective migration as epithelial-like sheets, potentially facilitating rapid establishment of the facial prominences. These cellular behaviours are unique amongst amniotes but resemble patterns in anamniotes which similarly exhibit accelerated craniofacial development to support early feeding. Marsupials appear to have evolved a similar mechanism of neural crest migration to facilitate their developmental heterochrony. These findings suggest that vertebrate neural crest migration may be shaped by the pace of craniofacial development during embryogenesis rather than phylogeny, providing new perspectives on neural crest plasticity and the developmental mechanisms driving craniofacial diversity across vertebrates.

developmental biology↗

bioRxiv2025

High-Yield Induced Ovulation in Adult Fat-Tailed Dunnarts by PMSG Treatment Combined with Estrus Synchronization

The fat-tailed dunnart, Sminthopsis crassicaudata, is an emerging laboratory-based marsupial model for research on comparative biology, reproduction and conservation. In females, the reproductive cycle lasts 31 days and approximately 10 oocytes are ovulated per cycle. Assisted reproductive technologies (ART) play a crucial role in marsupial conservation, but developing protocols to harvest large numbers of oocytes remains a key challenge. Specifically, producing sufficient mature metaphase II (MII) oocytes in dunnarts continues to be difficult. Ovarian follicle stimulation is common practice to achieve superovulation in many species and typically requires treatment of prepubertal female animals to avoid the impacts of endogenous hormone cycling. Alternatively, adult females can be stimulated during the intermediate or follicular phase. In this study, we aimed to develop a high-yield induced-ovulation protocol to collect higher number of MII oocytes from adult, cycling, female dunnarts. We first synchronized the female dunnart reproductive cycles using luteinizing hormone-releasing hormone (LHRH). The reproductive cycles were monitored by examining cytology of vaginal lavage samples. After administering four LHRH injections given at three-day intervals, 88.9% (n=36) of the adult female dunnarts responded to the treatment, with their estrous cycles synchronized at the diestrous stage. We then induced ovarian follicle development through two PMSG injections over 6 days, followed by hCG administration to trigger ovulation. By combining estrous cycle synchronization with PMSG stimulation, we achieved 77.8% (n=36) ovulation success and obtained an average of 20.1{+/-}9.1 (n=28) MII oocytes per adult dunnart. These data demonstrated that estrous cycle synchronization followed by the PMSG-hCG treatment yields consistent, highly efficient induced-ovulation in adult dunnarts. This approach of combining estrus synchronization and follicle stimulation to produce sufficient MII oocytes for ART purpose could be applied to other valuable marsupial species to support conservation efforts. Summary SentenceSuperovulation and robust production of mature MII oocytes can be induced by 10-day estrus synchronization using LHRH followed by 6-day PMSG stimulation of follicle growth in adult fat-tailed dunnarts, a marsupial species. Graphical Abstract O_FIG O_LINKSMALLFIG WIDTH=200 HEIGHT=93 SRC="FIGDIR/small/671172v1_ufig1.gif" ALT="Figure 1"> View larger version (33K): org.highwire.dtl.DTLVardef@14c6685org.highwire.dtl.DTLVardef@decf75org.highwire.dtl.DTLVardef@64330org.highwire.dtl.DTLVardef@12538a4_HPS_FORMAT_FIGEXP M_FIG C_FIG

developmental biology↗

bioRxiv2025

Dissecting functional regulatory convergence over 160 million years of therian evolution

Understanding the molecular mechanisms underpinning convergent traits can provide insight into the predictability of the evolutionary process. The thylacine, an extinct marsupial carnivore, has been long known to have a very similar craniofacial morphology to that of eutherian canids, despite having diverged{approx} 160 million years ago. Using a massively parallel reporter assay (MPRA), we tested the regulatory potential of a set of previously identified highly conserved craniofacial enhancers that showed convergent sequence acceleration in thylacine and wolf (TWARs). We compared orthologous sequences from six different taxa, including outgroup taxa with non-convergent craniofacial phenotypes (Tasmanian devil and giant panda) and ancestral reconstructions for marsupial and placental carnivores (Dasyuromorphia and Carnivora). Dense 10bp tiling allowed us to thoroughly examine features associated with activity, including percentage GC content and transcription factor binding motifs turnover. We identified marked conservation of levels and patterns of regulatory activity across all six taxa, as well as multiple cases of differentially active TWARs within each clade, with both thylacine and wolf driving functional divergence. However, evidence of convergent divergence was limited to a set of neighbouring TWARs near the neural crest gene Phox2b - one of which exhibited reduced activity in the wolf, and the other in the thylacine. Ultimately our findings suggest that shared gene regulatory potential is not a feature of these convergently accelerated regions in the thylacine and wolf.

genomics↗

bioRxiv2025

Generation and Assessment of High-Quality Fat-Tailed Dunnart Oocytes Following Superovulation in Prepubertal Animals

The fat-tailed dunnart, Sminthopsis crassicaudata, is a mouse-sized, polyovular, solitary dasyurid marsupial found in central and southern Australia. With the establishment of a chromosome-scale genome assembly, induced pluripotent stem cells, and targeted genetic editing, the dunnart is emerging as the laboratory marsupial model for comparative developmental, reproductive and conservation biology. The development of assisted reproductive technologies (ART) are critical to achieving these goals in this species. ART requires a large number of mature oocytes which are typically collected through stimulated and synchronised female reproductive cycles. While protocols for induced-ovulation or superovulation are standard in many placental mammals, there are no methods to date designed for marsupials. In the present study, prepubertal dunnarts were stimulated with pregnant mare serum gonadotrophin and human chronic gonadotrophin across 6 different treatment regimens. Our best regimen resulted in over 70% of prepubertal dunnarts ovulating with 82% normal oocytes. When the primed females were mated with stud males, 4-cell stage embryos were collected 48 h post-hCG administration. At around 96 h post-hCG, 50% (n=8) and 78% (n=9) of the embryos developed to blastocysts. Our results demonstrated successful stimulation of ovulation and mature oocyte collection in prepubertal dunnarts. Furthermore, we confirmed developmental competence of the induced ovulated oocytes through to at least the blastocyst stage. These findings represent the first robust hormonal regimen for predictable oocyte generation in any marsupial and will significantly contribute to the use of the dunnart in developmental and conservation biology.

developmental biology↗

bioRxiv2025

Loss-of-function mutations in ASIP and MC1R are associated with coat color variation in marsupials.

Pigment production in mammalian hair follicles is governed in part by interactions between Agouti Signalling Protein (ASIP) and the Melanocortin 1 Receptor (MC1R). The most common coat colours in mammals result from alternating bands of dark eumelanin and light pheomelanin within individual hairs. However, coats dominated by a single type of melanin have arisen several times. Here, we examine the genetic basis of two instances among the marsupials: a melanistic morph of the eastern quoll (Dasyurus viverrinus) found at high frequency in the wild, and a rare case of fixed xanthism in the marsupial moles. In the eastern quoll, we show that a deletion encompassing part of the ASIP coding sequence likely explains melanism in this species. Notably, this mutation is convergent with that recently discovered in its dark-coated relative, the Tasmanian devil (Sarcophilus harrisii). Conversely, we show that a nonsense mutation which severely truncates MC1R in the southern marsupial mole (Notoryctes typhlops) is a strong candidate driver of its pheomelanin-predominant coat. Together with other recent findings, our results suggest that loss-of-function mutations have occurred repeatedly within the marsupials, representing an important mechanism underpinning coat colour variation.

genomics↗

bioRxiv2024

Marsupial limb patterning redefines the necessity of lateral plate mesoderm subdivision for limb formation

The tetrapod limb has long served as a model for elucidating molecular and cellular mechanisms driving tissue patterning, development and evolution. While significant advances have been made in understanding the drivers of limb initiation, outgrowth, and patterning, the early morphogenetic processes that transform the lateral plate mesoderm (LPM) into limb fields remain less resolved. Marsupial mammals provide a unique opportunity to investigate these foundational processes due to their accelerated forelimb development, driven by the functional demands of altricial neonates to crawl into the pouch at birth. Heterochronic formation of the forelimbs occurs prior to development of other surrounding structures, offering unparalleled insights into the plasticity of limb field specification. Here, we reveal that marsupial limb initiation and outgrowth bypasses physical subdivision of the LPM, a process previously considered critical for tetrapod limb formation. Instead, limb development proceeds through early activation of LPM-associated genes and proliferation before coelom formation, demonstrating remarkable morphogenetic plasticity. This evolutionary adaptation enables heterochronic limb development, redefining conserved processes to meet extreme functional constraints. These findings challenge previous models of tetrapod limb specification, highlighting the evolutionary plasticity of limb patterning mechanisms and reshaping our understanding of how selective pressures influence foundational developmental events.

developmental biology↗

bioRxiv2024

Enrichment of spermatogonial stem cells and staging of the testis cycle in a dasyurid marsupial, the fat-tailed dunnart

There is increasing interest in use of marsupial models in research, for use in next-generation conservation by improving fitness through genetic modification, and in de-extinction efforts. Specifically this includes dasyurid marsupials such as the Thylacine, Tasmanian devil, quolls and the small rodent-like dunnarts. Technologies for generating genetically modified Australian marsupials remains to be established. Given the need to advance research in this space, the fat-tailed dunnart (Sminthopsis crassicaudata) is being established as a model for marsupial spermatogonial stem cell isolation, modification and testicular transplantation. This species is small (60-90mm body size), polyovulatory (8-12 pups per birth), and can breed in standard rodent facilities when housed in a 12:12 light cycle. To develop the fat tailed dunnart as a model for next-generation marsupial conservation, this study aimed to enrich dunnart spermatogonial stem cells from whole testis digestions using a fluorescent dye technology and fluorescence-activated cell sorting. This approach is not dependent on antibodies or genetic reporter animals that are limiting factors when performing cell sorting on species separated from human and mouse by large evolutionary timescales. This study also assessed development of spermatogonia and spermatogenesis in the fat-tailed dunnart, by making the first definition of the cycle of the seminiferous epithelium in any dasyurid. Overall, this is the first detailed study to assess the cycle of dasyurid spermatogenesis and provides a valuable method to enrich marsupial spermatogonial stem cells for cellular, functional and molecular analysis.

cell biology↗

bioRxiv2024

Genetically engineered resistance to bufotoxin in marsupial ATP1A1

The introduction of the bufotoxin-secreting cane toad (Rhinella marina) to Queensland in 1935 has had a devastating impact on wildlife in the Australian tropics. Having evolved for millions of years in the absence of cane toads or other bufotoxin-secreting organisms, many of the Australias native predators that include cane toads in their diet suffered large population declines following cane toad invasion to their habitat. One marsupial species, the northern quoll (Dasyurus hallucatus), is now classified as endangered (IUCN Red List) largely due to bufotoxin ingestion. This study aimed to introduce bufotoxin resistance into a marsupial cell line by editing part of the ATP1A1 gene encoding the extracellular H1-H2 domain - the binding target of bufotoxin. To this end, CRISPR prime editing was used to replace the part of the wildtype ATP1A1 gene encoding the H1-H2 domain in fibroblasts of a related marsupial model, the fat-tailed dunnart (Sminthopsis crassicaudata), with modifications known to be associated with bufotoxin resistance. The genetically modified cell population showed a >45-fold increase in resistance to bufalin (an active component of bufotoxin) compared to wild type. This study provides a proof of concept towards engineering genetic resistance in the northern quoll to halt or even reverse its current population decline.

bioengineering↗

bioRxiv2023

De novo transcriptome assembly and genome annotation of the fat-tailed dunnart (Sminthopsis crassicaudata)

Marsupials exhibit highly specialized patterns of reproduction and development, making them uniquely valuable for comparative genomics studies with their sister lineage, eutherian (also known as placental) mammals. However, marsupial genomic resources still lag far behind those of eutherian mammals, limiting our insight into mammalian diversity. Here, we present a series of novel genomic resources for the fat-tailed dunnart (Sminthopsis crassicaudata), a mouse-like marsupial that, due to its ease of husbandry and ex-utero development, is emerging as a laboratory model. To enable wider use, we have generated a multi-tissue de novo transcriptome assembly of dunnart RNA-seq reads spanning 12 tissues. This highly representative transcriptome is comprised of 2,093,982 assembled transcripts, with a mean transcript length of 830 bp. The transcriptome mammalian BUSCO completeness score of 93% is the highest amongst all other published marsupial transcriptomes. Additionally, we report an improved fat-tailed dunnart genome assembly which is 3.23 Gb long, organized into 1,848 scaffolds, with a scaffold N50 of 72.64 Mb. The genome annotation, supported by assembled transcripts and ab initio predictions, revealed 21,622 protein-coding genes. Altogether, these resources will contribute greatly towards characterizing marsupial biology and mammalian genome evolution.

genomics↗

bioRxiv2023

Reference genome of the endangered eastern quoll (Dasyurus viverrinus)

The eastern quoll (Dasyurus viverrinus) is an endangered marsupial mesopredator native to Australia. Since the extirpation of the last mainland Australian populations in the late 20th century, wild populations of this species have been restricted to two islands at the far southern end of its historical range. Eastern quolls are the subject of captive breeding programs and attempts have recently been made to re-establish a population in mainland Australia through translocations. However, few resources currently exist to guide the genetic management of this species. Here, we generated a chromosome-scale reference genome for the eastern quoll, along with gene annotations supported by multi-tissue transcriptomes. Through comparisons with related species, we find that our reference genome is among the most complete marsupial assemblies currently available. Using this assembly, we infer the species demographic history and identify potential evidence of a long-term decline beginning in the late Pleistocene. Finally, we identify a deletion at the ASIP locus that likely drives differences in pelage color between the eastern quoll and the closely related Tasmanian devil (Sarcophilus harrisii). The genomic resources we present are valuable new tools for evolutionary and conservation genomic studies.

genomics↗

bioRxiv2023

Cis-regulatory landscapes of the fat-tailed dunnart and mouse provide insights into the drivers of craniofacial heterochrony

Marsupials and placental mammals exhibit significant differences in reproductive and life history strategies. Marsupials are born highly underdeveloped after an extremely short period of gestation, leading to prioritization of the development of structures critical for post-birth survival in the pouch. Critically, they must undergo accelerated development of the oro-facial region compared to placentals. Previously we described the accelerated development of the oro-facial region in the carnivorous Australian marsupial, the fat-tailed dunnart Sminthopsis crassicaudata that has one of the shortest gestations of any mammal. By combining genome comparisons of the mouse and dunnart with functional data for the enhancer-associated chromatin modifications, H3K4me3 and H3K27ac, we investigated divergence of craniofacial regulatory landscapes between these species. This is the first description of genome-wide face regulatory elements in a marsupial, with 60,626 putative enhancers and 12,295 putative promoters described. We also generated craniofacial RNA-seq data for the dunnart to investigate expression dynamics of genes near predicted active regulatory elements. While genes involved in regulating facial development were largely conserved in mouse and dunnart, the regulatory landscape varied significantly. Additionally, a subset of dunnart-specific enhancers were associated with genes highly expressed only in dunnart relating to cranial neural crest proliferation, embryonic myogenesis and epidermis development. Comparative RNA-seq analyses of facial tissue revealed dunnart-specific expression of genes involved in the development of the mechanosensory system. Accelerated development of the dunnart sensory system likely relates to the sensory cues received by the nasal-oral region during the postnatal journey to the pouch. Together these data suggest that accelerated face development in the dunnart may be driven by dunnart-specific enhancer activity. Our study highlights the power of marsupial-placental comparative genomics for understanding the role of enhancers in driving temporal shifts in development.

developmental biology↗

bioRxiv2022

A chromosome-scale hybrid genome assembly of the extinct Tasmanian tiger (Thylacinus cynocephalus)

The extinct Tasmanian tiger or thylacine (Thylacinus cynocephalus) was a large marsupial carnivore native to Australia. Once ranging across parts of the mainland, the species remained only on the island of Tasmania by the time of European colonization. It was driven to extinction in the early 20th century and is an emblem of native species loss in Australia. The thylacine was a striking example of convergent evolution with placental canids, with which it shared a similar skull morphology. Consequently, it has been the subject of extensive study. While the original thylacine assemblies published in 2018 enabled the first exploration of the species genome biology, further progress is hindered by the lack of high-quality genomic resources. Here, we present a new chromosome-scale hybrid genome assembly for the thylacine, which compares favorably with many recent de novo marsupial genomes. Additionally, we provide homology-based gene annotations, characterize the repeat content of the thylacine genome and show that, consistent with demographic decline, the species possessed a low rate of heterozygosity even compared to extant, threatened marsupials. SignificanceThe lack of high-quality genomes for extinct species inhibits research into their biology. Moreover, marsupials are underrepresented among sequenced genomes. Here, we present a new, chromosome-scale thylacine genome. This high-quality assembly is a valuable new resource for studies on marsupial carnivores.

genomics↗