Cold Spring Harbor Laboratory  
Contact Us | Faculty & Staff Directory

Media Contact

Public Affairs


Leemor Joshua-Tor
Professor & HHMI Investigator

Ph.D., The Weizmann Institute of Science, 1991
Areas of Research:
Structural biology; nucleic acid regulation; RNAi; molecular recognition; X-ray crystallography

View Faculty Page


Follow us on

  facebook-icon twitter-icon instagram-icon3 youtube-icon wordpress-icon2
  rss-icon email-icon linkedin-icon flipboard icon

Freeze-frames of enzymes in action have implications for a new cancer treatment concept

TUTase enzymes interact with let-7, a regulator of development; targeting them could help control certain cancers

Cold Spring Harbor, NY — Over millions of years of evolution, cells have developed myriad ways of regulating the processes that enable them to thrive. Especially useful tools have been saved, or “conserved,” over the eons, so that today we can find them in a broad spectrum of life forms, from the very primitive to the most complex.

Research published July 3, 2017 by structural biologists at Cold Spring Harbor Laboratory (CSHL) sheds light on how one such conserved mechanism works, with implications for the development of new cancer drugs.

TUTase enzymeUsing x-ray crystallography, Joshua-Tor’s team has captured the equivalent of freeze-frames of enzymes called TUTases in two different modes. In one mode (LEFT), the TUTase enzyme (consisting of pink and blue/green subunits surrounded by a dotted line) adds a single uridine (“U”) nucleotide to a precursor of the micro RNA let-7 (purple and orange helix). The addition of a single “U” leads to the production of a mature let-7 micro RNA, in turn supporting the process in which a stem cell differentiates into a specialized cell. In its other mode (RIGHT) a TUTase enzyme associates with a protein called Lin28, leading to the addition of 30 “U”s to a let-7 precursor. This targets it for destruction – essential for stem cells to retain their ability to proliferate indefinitely. The TUTases are potential targets in cancer cells, which seem to acquire the stem-like ability to proliferate. (click to enlarge)

Led by CSHL Professor and Howard Hughes Medical Institute Investigator Leemor Joshua-Tor, the team used x-ray crystallography to capture the equivalent of freeze-frames of a class of enzymes called TUTases. The pictures, at the resolution of individual atoms, shows them interacting with other molecules to regulate the activity of an important small RNA molecule called let-7.

Let-7, a microRNA, is a regulator of genes important in development. When expressed in humans, it’s part of the process in which our stem cells differentiate into the various specialized cell types that populate our organs. In contexts in which it’s important for stem cells to maintain their “stem-ness”—their ability to give rise indefinitely to more stem cells—let-7 needs to be deactivated.

Let-7 is of special interest because its deactivation in cancer cells is thought by some to confer upon those cells the stem cell-like property of being able to proliferate indefinitely. This has focused attention on understanding the mechanisms regulating whether let-7 is active or inactive.

The team’s pictures show how TUT4 and TUT7—two of the TUTase enzymes—act differently in the two contexts. In a differentiating cell, the TUTases correct a small genetically induced defect in the sequence of many let-7 precursors, enabling mature let-7 microRNAs to be generated. Those defects are ameliorated when a TUTase adds a single uridine (“U”) molecule to the sequence of a let-7 precursor.

In a stem cell destined to retain its stem-ness, one of the TUTases adds not one but 30 uridines to the let-7 precursor, in this way marking it for destruction by another enzyme. “We have been able to capture the TUTases in these two different modes of action,” says Joshua-Tor.

Joshua-Tor explains that TUTases are promising targets for new cancer therapies. In kidney and lung cancer cells, for example, in which let-7 levels are far below normal, TUTases involved in marking let-7 for destruction could perhaps be inhibited. Having extremely high resolution images of how they act in the molecular dance should help in that effort.

The team included first author Christopher Faehnl, a CSHL Research Investigator, and former Watson School of Biological Sciences student Jack Walleshauser. The work was supported by NIH grant R01-GM114147; the Cold Spring Harbor Laboratory Women in Science Award; and the Watson School of Biological Sciences.

“Multi-domain utilization by TUT4 and TUT7 in control of let-7 biogenesis” appears July 3, 2017 in Nature Structural and Molecular Biology. The authors are: Christopher R. Faehnle, Jack Walleshauser and Leemor Joshua-Tor. The paper can be accessed at:

About Cold Spring Harbor Laboratory

Founded in 1890, Cold Spring Harbor Laboratory has shaped contemporary biomedical research and education with programs in cancer, neuroscience, plant biology and quantitative biology. Home to eight Nobel Prize winners, the private, not-for-profit Laboratory employs 1,100 people including 600 scientists, students and technicians. The Meetings & Courses Program annually hosts more than 12,000 scientists. The Laboratory's education arm also includes an academic publishing house, a graduate school and the DNA Learning Center with programs for middle and high school students and teachers. For more information, visit

Written by: Peter Tarr, Senior Science Writer | This email address is being protected from spambots. You need JavaScript enabled to view it. | 516-367-8455