Search bioRxiv⌕ Search

Biology subjects

Cheong, E.

Publications and source records attributed to Cheong, E..

2 recordsLinked to original sources

Development of novel high-resolution melting markers for the assessment of hybridization between Mauremys sinensis and Mauremys reevesii in South Korea

The Chinese striped-necked turtle Mauremys sinensis was first reported in the wild in South Korea in 2012. Owing to its potential to hybridize with the native and endangered Mauremys reevesii in South Korea, leading to ecosystem disturbance, M. sinensis was designated as an ecosystem-disturbing species (EDS; hereafter) in 2020. Such hybridization between M. sinensis and M. reevesii has previously been reported in Taiwan. To protect and conserve the native South Korean M. reevesii population, the extent of its hybridization needed to be examined. Therefore, we developed novel high-resolution melting markers to elucidate the status of hybridization between Mauremys sinensis and Mauremys reevesii in South Korea. We identified the presence of M. sinensis, M. reevesii, and their hybrid across 47 sites in South Korea. Among these sites, five locations were confirmed as areas of sympatry for both M. sinensis and M. reevesii, with one hybrid individual identified at the Jeonju-si site. In total, hybrids were identified at four different sites. For more definitive species identification, blood samples were collected from the specimens and subjected to mitochondrial DNA (mtDNA) cytochrome c oxidase subunit I (COI) gene and nuclear DNA (nDNA) R35 gene analysis, leading to the identification of two more hybrids from two other sites. To date, no hybrids of M. sinensis have been confirmed to reproduce in the wild, yet this requires further research for validation. The high-resolution melting (HRM) marker in the R35 gene developed in this study yielded three distinct curves that were designated as M. sinensis, M. reevesii, and M. sinensis x M. reevesii, aligning with those of the R35 gene sequencing. The novel markers developed in this study serve as a valuable tool that can be used in future research on rapid detection of hybridization.

zoology↗

IQSEC3 Mediates Npas4-dependent GABAergic Synaptic Transmission and Depressive-like Behavior

Organization of mammalian inhibitory synapses is thought to be crucial for normal brain functions, but the underlying molecular mechanisms have been still incompletely understood. IQSEC3 (IQ motif and Sec7 domain 3) is a guanine nucleotide exchange factor for ADP-ribosylation factor (ARF-GEF) that directly interacts with gephyrin. Here, we show that GABAergic synapse-specific transcription factor, Npas4 (neuronal PAS domain protein 4) directly binds to the promoter of Iqsec3 and regulates its transcription. Strikingly, an enriched environment (EE) induced Npas4 upregulation and concurrently increased IQSEC3 protein levels specifically in mouse CA1 stratum oriens layer somatostatin (SST)-expressing GABAergic interneurons, which are compromised in Npas4-knockout (KO) mice. Moreover, expression of wild-type (WT) IQSEC3, but not a dominant-negative (DN) ARF-GEF-inactive mutant, rescued the decreased GABAergic synaptic transmission in Npas4-deficient SST interneurons. Concurrently, expression of IQSEC3 WT normalized the altered GABAergic synaptic transmission in dendrites, but not soma, of Npas4-deficient CA1 pyramidal neurons. Furthermore, expression of IQSEC3 WT, but not IQSEC3 DN, in SST-expressing interneurons in CA1 SST Npas4-KO mice rescued the altered anxiety-like behavior. Collectively, our results suggest that IQSEC3 is a key GABAergic synapse component that is directed by Npas4 activity- and ARF activity-dependent gene programs in SST-expressing interneurons to orchestrate the functional excitation-to-inhibition balance.

neuroscience↗