Latest Updates
-
Heatwave Alert: Why Your Phone and Laptop Are Overheating Right Now -
National Anti-Terrorism Day 2026: How Rajiv Gandhi’s Assassination Sparked A Nationwide Call For Peace -
International Tea Day 2026: Here's What Drinking Tea First Thing In The Morning Does To Your Gut -
Horoscope for Today May 21, 2026 - Curiosity Rises, Plans Shift -
Paneer Lababdar Recipe: Creamy Restaurant-Style Curry Made Easy -
Mouni Roy’s Cannes 2026 Patola Gown Took 300 Hours To Craft — The Story Of Gujarat’s GI-Tagged Weave -
Bread Pizza Recipe: Your Instant Snack Hack -
India's Hottest City Hit 47.6°C Today — This Is What Heatstroke Looks Like -
Exclusive: Rubina Dilaik Said Yes To The Ward In Seconds: Here's The Raw Truth Behind Why -
PM Modi Turns Viral ‘Melodi’ Nickname Real With Melody Gift To Meloni, Inside India’s Iconic Toffee Origin
A New Discovery In Genetic Mutation

According to the researchers, the gene, called hSDH5, is required for activation of an enzyme complex that plays a critical role in the chemical reactions that take place within cells to convert biochemical energy into usable energy. Dr. Jared Rutter, the lead author of the study explains, "Defects in mitochondria, the power sources of the cell, have been implicated in a variety of human disorders, including cancer."
The study, however, involved the use of yeast Saccharomyces cerevisiae, in order to study mitochondrial functions, before going back to humans and determining whether the same had relevance with humans too. Then came the results: They first characterized a mitochondrial protein called Sdh5 in yeast and then moved on to study its potential role in human disease.
This was not the end. Rutter and his colleagues discovered that, in yeast, the Sdh5 protein is needed for the S.D.H. complex to function normally. "The amino acid sequence of yeast Sdh5," said the man "Is 44 percent identical to its human counterpart, which we've named hSDH5." He adds:"Previous genetic studies have shown that the hereditary s PGL1, PGL3, and PGL4 are associated with mutations causing loss of S.D.H. Activity." He concludes: "Although the gene for PGL2 had not been identified, we knew that it was located on the same chromosome as the hSDH5 gene."
Rutter and his colleagues sequenced the hSDH5 gene in three individuals with PGL2. Of the 45 individuals within the affected lineage who inherited the mutation, 33 have developed PGL2, providing strong evidence that hSDH5 is the PGL2 gene.
AGENCIES
Disclaimer: The information provided in this article is for general informational and educational purposes only and is not intended as a substitute for professional medical advice, diagnosis, or treatment. Always seek the advice of your physician or a qualified healthcare provider with any questions you may have regarding a medical condition.



Click it and Unblock the Notifications