98%
921
2 minutes
20
The Parkin RBR E3 Ubiquitin Protein Ligase gene, the second largest gene within the human genome, plays a crucial role in physiological processes and is implicated in neurodegenerative pathologies, notably Parkinson's disease. The average size of this gene is approximately 1,300,000 base pairs (bp), while one of its messengers RNA (mRNAs) measures only 4,178 bp. Large Introns suggest the presence of transcriptional elements and Exons that exhibit interspecies variations, similar to the Dystrophin gene. In silico analysis of the Introns within the PRKN gene across 16 primate species revealed a largely conserved organization, a finding further substantiated by their phase patterns. Within these Introns, 420 open reading frames (ORFs) were identified, encompassing 1,454 Exons in the sense direction ranging between 1 to 12. These species-shared ORFs encode for domains primarily associated with phosphorylation and myristoylation, among others. The phylogeny of PRKN corresponds with other ones previously reported, correlating with bioinformatic analyses. The structures, characterized for the first time for the PRKN Introns, may be implicated in cellular functions that have not been yet experimentally determined. Furthermore, these structures may be associated with diseases arising from their mutational patterns. This approach provides a valuable contribution to the design of experimental validations.
Download full-text PDF |
Source |
---|---|
http://dx.doi.org/10.1109/TCBBIO.2025.3543468 | DOI Listing |
Mol Psychiatry
September 2025
National Center for PTSD, Behavioral Science Division, VA Boston Healthcare System, Boston, MA, 02130, USA.
Glial fibrillary acidic protein (GFAP) is an astrocytic marker that can be assessed in blood using single molecule array technology. Recent studies suggest that individuals with posttraumatic stress disorder (PTSD) have suppressed circulating levels of this CNS biomarker. This study examined the hypothesis that PTSD and plasma GFAP levels share common genetic and epigenetic pathways.
View Article and Find Full Text PDFComput Biol Med
September 2025
Institute of Biotechnology, Department of Medical Biotechnology, SIMATS Engineering, Saveetha Institute of Medical and Technical Sciences, Saveetha University, Chennai, 602105, Tamil Nadu, India. Electronic address:
Small humanin-like peptide-6 (SHLP6), is derived from the mitochondrial genome. The 3D structure of SHLP6 was evaluated using PEPstr, with homology modeling predicting a Cyt-C structure with a DOPE score of -645.717 and a GA341 score of 0.
View Article and Find Full Text PDFFront Neurol
August 2025
Medical Sciences Postgraduate Program, Federal University of Rio Grande do Sul, Porto Alegre, Brazil.
Background: Autonomic symptoms are among the most important factors determining the quality of life in patients with Parkinson's disease (PD). This study aimed to assess the profile of autonomic dysfunction symptoms in three groups of patients with genetic PD, carrying mutations in , , and genes, compared with subjects with sporadic PD.
Methods: This case-control observational secondary analysis of prospectively collected data was performed on 742 patients (485 in the sporadic group, 165 in the LRRK2 group, 85 in the GBA group, and nine in the PRKN group).
Zhongguo Zhong Yao Za Zhi
July 2025
Yunnan Provincial Academy of Science and Technology Kunming 650051, China.
This study aimed to investigate the effects of caffeoylquinic acids from Erigeron breviscapus(EBCQA) on cognitive impairment and mitochondrial dysfunction in Alzheimer's disease(AD), and to explore its underlying mechanisms. The impacts of EBCQA on paralysis, β-amyloid(Aβ) oligomerization, and mRNA expression of mitophagy-related genes [PTEN-induced putative kinase 1(PINK1) homolog-encoding gene pink-1, Parkin homolog-encoding gene pdr-1, Bcl-2 interacting coiled-coil protein 1(Beclin 1) homolog-encoding gene bec-1, microtubule-associated protein 1 light chain 3(LC3) homolog-encoding gene lgg-1, autophagic adapter protein 62(p62) homolog-encoding gene sqst-1] were examined in the AD Caenorhabditis elegans CL4176 model, along with mitochondrial functions including adenosine triphosphate(ATP) content, enzyme activities of mitochondrial respiratory chain complexes Ⅰ,Ⅲ, and Ⅳ, and mitochondrial membrane potential. Additionally, the effects of EBCQA on the green fluorescent protein(GFP)/red fluorescent protein from Discosoma sp.
View Article and Find Full Text PDFBrain Behav
September 2025
Department of Neurology, Renji Hospital, School of Medicine, Shanghai Jiao Tong University, Shanghai, China.
Background: PRKN and PINK1 gene mutations have been associated with Parkinson's disease (PD), particularly early-onset PD (EOPD).
Objectives: To describe the clinical and molecular features of a Chinese patient with EOPD who had uncommon PRKN and PINK1 mutations.
Methods: The patient's clinical history was reviewed, and whole-exome sequencing was performed to identify genetic mutations.