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Biology subjects

Alshehri, M.

Publications and source records attributed to Alshehri, M..

2 recordsLinked to original sources

HID1 domain-containing protein 1 is required for normal cell proliferation in Schizosaccharomyces pombe

HID1 domain-containing protein 1 (HID1) is a Golgi apparatus (GA) protein involved in the trafficking of cellular material. From reduced expression in cancer cell lines, it had been proposed to be a tumor suppressor in humans. In contrast, it is required for normal larval development of Caenorhabditis elegans, thereby raising an apparent contradiction for HID1 function regarding the inhibition or maintenance of cell proliferation. An extensive comparison of publicly available gene expression data revealed that HID1 transcript levels in cancer cell lines were not representative of those in primary tumors, and the gene is amplified in many primary tumors. These findings question the role for its expression to suppress cell proliferation. Subsequently, we employed the model S. pombe to explore the role of HID1 in cell proliferation. The knock-out mutant hid1{Delta} exhibited a reduced proliferation phenotype due to a prolonged lag-phase but, eventually, attained parent strain rates of apparent proliferation. RNAseq-based transcriptomics revealed that hid1{Delta} retained features of metabolically stressed cells with quiescence-like transcriptional regulation. A label-free proteomic analysis revealed a lack of various membrane proteins suggesting cells with compromised Golgi apparatus (GA) function. The inability of hid1{Delta} to grow on agar containing a standard minimal medium suggested a link to metabolic deficiency. These findings point to a hid1{Delta}-related perturbation in GA function that compromises cell recovery from metabolic change.

genetics↗

Regulation of neural stem cell fate by the transcriptional repressor Capicua

Capicua (Cic) is a transcriptional repressor mutated in the brain cancer oligodendroglioma. Despite its cancer link, little is known of Cics function in the brain. Here, we investigated the relationship between Cic expression and cell type specification in the brain. Cic is strongly expressed in astrocytic and neuronal lineage cells but is more weakly expressed in stem cells and oligodendroglial lineage cells. Using a new conditional Cic knockout mouse, we show that forebrain-specific Cic deletion increases proliferation and self-renewal of neural stem cells. Furthermore, Cic loss biases neural stem cells toward glial lineage selection, expanding the pool of oligodendrocyte precursor cells (OPCs). These proliferation and lineage selection effects in the developing brain are dependent on de-repression of Ets transcription factors. In patient-derived oligodendroglioma cells, CIC re-expression or ETV5 blockade decreases lineage bias, proliferation, self-renewal and tumorigenicity. Our results identify Cic is an important regulator of cell fate in neurodevelopment and oligodendroglioma, and suggest that its loss contributes to oligodendroglioma by promoting proliferation and an OPC-like identity via Ets overactivity.

cancer biology↗