NewsWorld
PredictionsDigestsScorecardTimelinesArticles
NewsWorld
HomePredictionsDigestsScorecardTimelinesArticlesWorldTechnologyPoliticsBusiness
AI-powered predictive news aggregation© 2026 NewsWorld. All rights reserved.
Trending
TrumpMajorMilitaryStrikesFebruaryIranAnnouncesIranianNewsAdditionalDigestSundayTimelineYearNuclearTargetingGameHumanoidGlobalMarketNipahLimitedChineseCampaign
TrumpMajorMilitaryStrikesFebruaryIranAnnouncesIranianNewsAdditionalDigestSundayTimelineYearNuclearTargetingGameHumanoidGlobalMarketNipahLimitedChineseCampaign
All Articles
en.shafaqna.com
Published 6 days ago

Key protein discovery solves mystery of deadly telomere diseases – Shafaqna English

en.shafaqna.com · Feb 16, 2026 · Collected from GDELT

Summary

Published: 20260216T213000Z

Full Article

February 16, 2026 | 6:31 PMFebruary 16, 2026 | 7:32 PM0 Shafaqna English- Scientists have identified a crucial protein that plays a previously unknown role in maintaining the protective caps on our chromosomes, called telomeres. A malfunction in this protein, known as RPA, leads to dangerously short telomeres, explaining the cause of certain deadly cancers and bone marrow disorders that were until now a mystery. Published in Science, the University of Wisconsin-Madison research used the AI tool AlphaFold to predict and then experimentally confirm that RPA is essential for stimulating telomerase, the enzyme that rebuilds telomeres. When RPA doesn’t work properly, telomerase cannot maintain telomere length, leading to genomic instability and disease. The discovery provides a clear biochemical explanation for patients with severe “short telomere” disorders like aplastic anemia and acute myeloid leukemia, whose conditions could not be previously diagnosed at the molecular level. “Now we have an answer,” said lead researcher Ci Ji Lim. Since the publication, clinicians worldwide have contacted the team to see if their patients’ illnesses stem from RPA mutations. The finding opens new avenues for precise genetic diagnosis and deepens the understanding of how chromosome stability is linked to human health and disease. Source: University of Wisconsin-Madison www.shafaqna.com


Share this story

Read Original at en.shafaqna.com

Related Articles

Science News1 day ago
This itch-triggering protein also sends signals to stop scratching

The TRPV4 protein’s dual nature, found in studies with mice, may complicate the hunt for human itch treatments

news-medical.net1 day ago
Brain injury protein in the blood could help estimate biological age in animals

Published: 20260221T033000Z

aol.com1 day ago
Scientists extracted DNA from mummified cheetah remains and made a surprising discovery

Published: 20260221T021500Z

sciencedaily.com3 days ago
Giant virus discovery could rewrite the origin of complex life

Published: 20260220T043000Z

Science News3 days ago
Machine learning streamlines the complexities of making better proteins

The framework predicts how proteins will function with several interacting mutations and finds combinations that work well together.

Science Daily4 days ago
Ancient DNA solves 5,500 year old burial mystery in Sweden

Ancient DNA from a Stone Age burial site in Sweden shows that families 5,500 years ago were more complex than expected. Many individuals buried together were not immediate family, but second- or third-degree relatives. One grave held a young woman alongside two children who were siblings—yet she wasn’t their mother. The discoveries hint at tight-knit communities where extended kin mattered deeply.