Search bioRxiv⌕ Search

Biology subjects

Larrigan, S.

Publications and source records attributed to Larrigan, S..

3 recordsLinked to original sources

An allelic series reveals the genetic requirement for Adnp in cortical neurogenesis and learning behavior

Transcriptional regulators and chromatin remodellers are among the most important risk gene categories across the genetic landscape of neurodevelopmental disorders (NDDs). The zinc finger and homeodomain transcription factor ADNP is prominently associated with Helsmoortel-Van der Aa Syndrome (HVDAS), which is characterized by intellectual disability and autism spectrum disorder. Heterozygous frameshifting mutations account for the majority of HVDAS mutations, but it remains unclear how HVDAS mutations affect ADNP dosage, and how dosage in turn relates to neurodevelopmental and behavioral phenotypes. Here, we compared an allelic series of Adnp cKOs and germline heterozygotes. Using a conditional allele, we first deleted Adnp throughout the neural tube using Nestin-Cre. At E15.5, cKO brains exhibited altered upper-layer neuron production. However, AdnpNestincKOs exhibited perinatal lethality, precluding further behavioral characterization. Next, we compared germline heterozygotes (gHets) versus cKOs generated using the Emx1-Cre driver. We found that AdnpDel/+and AdnpL822fs6/+ gHets exhibited cortical hypoplasia that was quantitatively identical, albeit less severe in comparison to AdnpEmxcKOs. In behavioral testing, AdnpEmx cKOs accordingly exhibited the strongest phenotypes, including hallmarks of elevated anxiety. However, both AdnpEmx cKOs and AdnpL822fs6/+ gHets exhibited remarkably similar sex-specific deficits in learning during Morris Water Maze testing. Taken together, our work suggests that cortical growth and learning represent core phenotypes shared across Adnp mutant models irrespective of dosage. Moreover, since Adnp mutant phenotypes closely correspond with our prior findings in Chd4 mutants, our results collectively suggest that Adnp regulates behavior via the ChAHP chromatin remodelling complex.

neuroscience↗

The ChAHP chromatin remodelling complex regulates neurodevelopmental disorder risk genes to scale the production of neocortical layers

Although chromatin remodellers are among the most important risk genes associated with neurodevelopmental disorders (NDDs), the roles of these complexes during brain development are in many cases unclear. Here, we focused on the recently discovered ChAHP chromatin remodelling complex. The zinc finger and homeodomain transcription factor ADNP is a core subunit of this complex, and de novo ADNP mutations lead to intellectual disability and autism spectrum disorder. However, germline Adnp knockout mice were previously shown to exhibit early embryonic lethality, obscuring subsequent roles for the ChAHP complex in neurogenesis. Here, we employed single cell transcriptomics, cut&run-seq, and histological approaches to characterize mice conditionally ablated for the ChAHP subunits Adnp and Chd4. We show that during neocortical development, Adnp and Chd4 orchestrate the production of late-born, upper-layer neurons through a two-step process. First, Adnp is required to sustain progenitor proliferation specifically during the developmental window for upper-layer cortical neurogenesis. Accordingly, we found that Adnp recruits Chd4 to genes associated with progenitor proliferation. Second, in postmitotic differentiated neurons, we define a network of risk genes linked to NDDs that are regulated by Adnp and Chd4. Taken together, these data demonstrate that ChAHP is critical for driving the expansion upper-layer cortical neurons, and for regulating neuronal gene expression programs, suggesting that these processes may potentially contribute to NDD etiology. HighlightsO_LIAdnp and Chd4 cKOs exhibit similar deficits in cortical growth C_LIO_LIAdnp sustains the proliferation of apical progenitors to scale the production of upper-layer neurons C_LIO_LIAdnp recruits Chd4 to genes involved in corticogenesis C_LIO_LIAdnp is a master regulator of risk genes associated with neurodevelopmental disorders C_LI

neuroscience↗

Divergent phenotypes in germline versus conditional mutant mouse models of Sifrim-Hitz- Weiss Syndrome

Chromatin remodellers are among the most important risk genes associated with neurodevelopmental disorders (NDDs), however, their functions during brain development are not fully understood. Here, we focused on Sifrim-Hitz-Weiss Syndrome (SIHIWES) - a brain overgrowth/intellectual disability disorder caused by mutations in the CHD4 chromodomain helicase gene. We utilized mouse genetics to excise the Chd4 ATPase/helicase domain - either in the germline, or conditionally in the developing telencephalon. Conditional heterozygotes exhibited little change in cortical size and cellular composition, and had only subtle behavioral phenotypes. Telencephalon-specific conditional knockouts had marked reductions in cortical growth, reduced numbers of upper-layer neurons, and exhibited alterations in anxiety and repetitive behaviors. Despite the fact that germline heterozygotes exhibited comparable growth defects, they were unaffected in these behaviors, but instead exhibited female-specific alterations in learning and memory. These data reveal unexpected phenotypic divergence arising from differences in the spatiotemporal deployment of loss-of-function manipulations, underscoring the importance of context in chromatin remodeller function during neurodevelopment. Graphical Abstract. O_FIG O_LINKSMALLFIG WIDTH=200 HEIGHT=90 SRC="FIGDIR/small/528754v1_ufig1.gif" ALT="Figure 1"> View larger version (21K): org.highwire.dtl.DTLVardef@ffdb72org.highwire.dtl.DTLVardef@1a0231corg.highwire.dtl.DTLVardef@613242org.highwire.dtl.DTLVardef@12ac3ab_HPS_FORMAT_FIGEXP M_FIG C_FIG

neuroscience↗