Post-transcriptional regulatory functions of mammalian pumilio proteins

AC Goldstrohm, TMT Hall, KM McKenney - TRENDS in Genetics, 2018 - cell.com
Mammalian Pumilio proteins, PUM1 and PUM2, are members of the PUF family of sequence-
specific RNA-binding proteins. In this review, we explore their mechanisms, regulatory …

RNA-binding proteins balance brain function in health and disease

R Schieweck, J Ninkovic… - Physiological reviews, 2021 - journals.physiology.org
Posttranscriptional gene expression including splicing, RNA transport, translation, and RNA
decay provides an important regulatory layer in many if not all molecular pathways …

Molecular logic of cellular diversification in the mouse cerebral cortex

DJ Di Bella, E Habibi, RR Stickels, G Scalia, J Brown… - Nature, 2021 - nature.com
The mammalian cerebral cortex has an unparalleled diversity of cell types, which are
generated during development through a series of temporally orchestrated events that are …

Multi-omic single-cell velocity models epigenome–transcriptome interactions and improves cell fate prediction

C Li, MC Virgilio, KL Collins, JD Welch - Nature biotechnology, 2023 - nature.com
Multi-omic single-cell datasets, in which multiple molecular modalities are profiled within the
same cell, offer an opportunity to understand the temporal relationship between epigenome …

Temporal patterning of apical progenitors and their daughter neurons in the developing neocortex

L Telley, G Agirman, J Prados, N Amberg, S Fièvre… - Science, 2019 - science.org
INTRODUCTION The cerebral cortex is a cellularly heterogeneous structure whose
neuronal circuits underlie high-order cognitive and sensorimotor information processing …

A single-cell transcriptomic atlas of human neocortical development during mid-gestation

D Polioudakis, L de la Torre-Ubieta, J Langerman… - Neuron, 2019 - cell.com
We performed RNA sequencing on 40,000 cells to create a high-resolution single-cell gene
expression atlas of developing human cortex, providing the first single-cell characterization …

Transcriptional priming as a conserved mechanism of lineage diversification in the developing mouse and human neocortex

Z Li, WA Tyler, E Zeldich, G Santpere Baró… - Science …, 2020 - science.org
How the rich variety of neurons in the nervous system arises from neural stem cells is not
well understood. Using single-cell RNA-sequencing and in vivo confirmation, we uncover …

Aberrant cortical development is driven by impaired cell cycle and translational control in a DDX3X syndrome model

ML Hoye, L Calviello, AJ Poff, NE Ejimogu… - Elife, 2022 - elifesciences.org
Mutations in the RNA helicase, DDX3X, are a leading cause of Intellectual Disability and
present as DDX3X syndrome, a neurodevelopmental disorder associated with cortical …

Conserved transcriptional regulation by BRN1 and BRN2 in neocortical progenitors drives mammalian neural specification and neocortical expansion

S Barão, Y Xu, JP Llongueras, R Vistein, L Goff… - Nature …, 2024 - nature.com
The neocortex varies in size and complexity among mammals due to the tremendous
variability in the number and diversity of neuronal subtypes across species. The increased …

[HTML][HTML] Cell-type-specific profiling of human cellular models of fragile X syndrome reveal PI3K-dependent defects in translation and neurogenesis

N Raj, ZT McEachin, W Harousseau, Y Zhou, F Zhang… - Cell reports, 2021 - cell.com
Transcriptional silencing of the FMR1 gene in fragile X syndrome (FXS) leads to the loss of
the RNA-binding protein FMRP. In addition to regulating mRNA translation and protein …