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SUN5, a testis-specific nuclear membrane protein, participates in recruitment and export of nuclear mRNA in spermatogenesis.

Acta Biochim Biophys Sin (Shanghai)

August 2024

Center for Experimental Medicine, Third Xiangya Hospital, Central South University, Changsha 410013, China.

Article Synopsis
  • Sun5, a testis-specific gene, is linked to acephalic spermatozoa syndrome (ASS) and plays a critical role in mRNA export in male germ cells.* -
  • Knockout mice studies show that loss of Sun5 leads to accumulation of poly(A) RNA in nuclei, resulting in lower sperm counts and motility issues.* -
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Transcription Factor yin-Yang 1 augments nucleoporin 93 oncogene activity and modulates bladder Cancer malignancy.

Toxicol In Vitro

August 2024

Department of Urology section, Dalian Friendship Hospital, Dalian, Liaoning 116001, China. Electronic address:

Objective: This study aims to investigate the functional interplay between transcription factor YY1 and nucleoporin 93 (NUP93) in regulating the malignancy of bladder cancer cells.

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Nuclear pore complex (NPC) biogenesis is a still enigmatic example of protein self-assembly. We now introduce several cross-reacting anti-Nup nanobodies for imaging intact nuclear pore complexes from frog to human. We also report a simplified assay that directly tracks postmitotic NPC assembly with added fluorophore-labeled anti-Nup nanobodies.

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As the innermost lining of the vasculature, endothelial cells (ECs) are constantly subjected to systemic inflammation and particularly vulnerable to aging. Endothelial health is hence vital to prevent age-related vascular disease. Healthy ECs rely on the proper localization of transcription factors via nuclear pore complexes (NPCs) to govern cellular behavior.

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Endothelial cells (ECs) form the innermost lining of the vasculature and serve a pivotal role in preventing age-related vascular disease. Endothelial health relies on the proper nucleocytoplasmic shuttling of transcription factors via nuclear pore complexes (NPCs). Emerging studies report NPC degradation with natural aging, suggesting impaired nucleocytoplasmic transport in age-related EC dysfunction.

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