Kinesin family member17 (KIF17), a homologous dimer of the kinesin-2 protein family, has important microtubule-dependent and -independent roles in spermiogenesis. Little is known about KIF17 in the mollusk, , a newly developed mariculture species in China. Here, we cloned the open reading frame of and its related gene, , and performed bioinformatics analysis on both. -KIF17 and -ACT are structurally conserved, indicating that they may be functionally conserved. The expression pattern of mRNA performed during spermiogenesis revealed their expression in diverse tissues, with the highest expression level in the coelomic fluid of . The expressions of and mRNA were relatively high during the breeding season (July-September), suggesting that -KIF17/ACT may be involved in spermatogenesis, particularly during spermiogenesis. Further analysis of mRNA via fluorescence in situ hybridization revealed the continuous expression of this mRNA during spermiogenesis, suggesting potential functions in this process. Immunofluorescence showed that -KIF17 co-localized with α-tubulin and migrated from the perinuclear cytoplasm to one side of the spermatid, forming the sperm tail. -KIF17 and -ACT also colocalized. KIF17 may participate in spermiogenesis of , particularly in nuclear reshaping and tail formation by interacting with microtubule structures similar to the manchette. Moreover, -KIF17 with -ACT is also involved in nuclear reshaping and tail formation in the absence of microtubules. This study provides evidence for the role of KIF17 during spermiogenesis and provides theoretical data for studies of the reproductive biology of . These findings are important for spermatogenesis in mollusks.
Download full-text PDF |
Source |
---|---|
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10779256 | PMC |
http://dx.doi.org/10.3390/ijms25010128 | DOI Listing |
J Biol Chem
December 2024
Center for Mitochondrial Biomedicine and Department of Otolaryngology-Head and Neck Surgery, the Fourth Affiliated Hospital, Zhejiang University School of Medicine, Yiwu, Zhejiang, China; Institute of Genetics, Zhejiang University International School of Medicine, Hangzhou, Zhejiang, China; Center for Genetic Medicine, Zhejiang University International Institute of Medicine, Yiwu, Zhejiang, China; Joint Institute of Genetics and Genomic Medicine between Zhejiang University and University of Toronto, Hangzhou, Zhejiang, China. Electronic address:
Human mitochondrial 12S ribosomal RNA (rRNA) 1555A>G mutation has been associated with aminoglycoside-induced and nonsyndromic deafness in many families worldwide. Our previous investigation revealed that the m.1555A>G mutation impaired mitochondrial translation and oxidative phosphorylation (OXPHOS).
View Article and Find Full Text PDFmSphere
December 2024
Department of Molecular Genetics, University of Toronto, Toronto, Ontario, Canada.
Unlabelled: The eukaryotic CCR4-NOT deadenylase complex is a highly conserved regulator of mRNA metabolism that influences the expression of the complete transcriptome, representing a prime target for a generalist bacterial pathogen. We show that a translocated bacterial effector protein, PieF (Lpg1972) of , directly interacts with the CNOT7/8 nuclease module of CCR4-NOT, with a dissociation constant in the low nanomolar range. PieF is a robust inhibitor of the DEDD-type nuclease, CNOT7, acting in a stoichiometric, dose-dependent manner.
View Article and Find Full Text PDFJ Radiat Res
December 2024
Fukushima University International Center, Fukushima University, 1 Kanayagawa, Fukushima 960-1296 Japan.
As Fukushima grapples with ongoing challenges related to reputational damage, it is becoming increasingly imperative to establish an effective means for global audiences to access, comprehend, and support the region's recovery efforts. To achieve this, Fukushima Prefecture has been strategically organizing educational tours tailored for international visitors, operating under the umbrella of ``Hope Tourism.'' These tours aim to bring about positive change by dispelling negative perceptions, offering a nuanced understanding of Fukushima's ongoing revitalization, and fostering connections between visitors and local residents.
View Article and Find Full Text PDFACS Nano
December 2024
State Key Laboratory of Supramolecular Structure and Material, College of Chemistry, Jilin University, Changchun 130012, China.
Front Immunol
December 2024
Liaoning Technology and Engineering Center for Tumor Immunology and Molecular Theranotics, Collaborative Innovation Center for Age-related Disease, Life Science Institute, Jinzhou Medical University, Jinzhou, Liaoning, China.
Introduction: ETAA1 is recruited to DNA damage sites via its RPA -binding and ATR -activating domain (AAD) motifs, where RPA binding is crucial for ETAA1's regulation of ATR activity.
Methods & Results: Our findings associate Programmed Death- Ligand1 (PD-L1) with the RPA1-ETAA1 axis, suggesting that upregulated RPA1 -dependent ETAA1 may facilitate PD-L1 nuclear accumulation. We observed strong correlations between ETAA1 and RPA1 with the components involved in HDAC2-mediated deacetylation, clathrin -dependent endocytosis, and PD-L1 nucleocytoplasmic shuttling, aligning with the established regulatory pathway of PD-L1 nuclear translocation.
Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!