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Protein Function Refuted

A mouse knockout calls into question the presumed function of a protein long considered important for steroid hormone biosynthesis.

Written byAbby Olena, PhD
| 2 min read

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TYPICAL TESTES: Control mouse testis (left) and TSPO-knockout testis (right) develop similarly, refuting long-held assumptions about TSPO’s function.KANAKO MOROHAKU, CORNELL UNIVERSITY

The paper K. Morohaku et al., “Translocator protein/peripheral benzodiazepine receptor is not required for steroid hormone biosynthesis,” Endocrinology, 155:15-20, 2013. The context The first step in steroid hormone production is the transportation of cholesterol into the mitochondria. For years, scientists have considered two candidates vital to this process: steroidogenic acute regulatory protein (StAR) and channel-like translocator protein (TSPO). Experiments in knockout mice showed that StAR, which binds cholesterol, is essential for hormone production. But the bulk of evidence regarding TSPO, found in the outer mitochondrial membrane, has been generated using cell lines because global TSPO knockout mice die as embryos. The surprise A team led by Vimal Selvaraj of Cornell University deleted TSPO only in the testicular Leydig cells of mice. Much to his surprise, ...

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Meet the Author

  • abby olena

    As a freelancer for The Scientist, Abby reports on new developments in life science for the website. She has a PhD from Vanderbilt University and got her start in science journalism as the Chicago Tribune’s AAAS Mass Media Fellow in 2013. Following a stint as an intern for The Scientist, Abby was a postdoc in science communication at Duke University, where she developed and taught courses to help scientists share their research. In addition to her work as a science journalist, she leads science writing and communication workshops and co-produces a conversational podcast. She is based in Alabama.  

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