More reprogramming clues (maybe)

One of the biggest holy grails in biology involves finding a means to generate pluripotent and infinitely replicating stem cells without generating an embryo. One Japanese team presented some potent clues last night at the linkurl:Keystone conference;http://www.keystonesymposia.org/Meetings/ViewMeetings.cfm?MeetingID=786 on stem cell biology -- but stem cell researchers will need a few more bread crumbs before they can put this potentially exciting information to use. linkurl:Shinya Yamanaka;ht

Written byAlison McCook
| 1 min read

Register for free to listen to this article
Listen with Speechify
0:00
1:00
Share
One of the biggest holy grails in biology involves finding a means to generate pluripotent and infinitely replicating stem cells without generating an embryo. One Japanese team presented some potent clues last night at the linkurl:Keystone conference;http://www.keystonesymposia.org/Meetings/ViewMeetings.cfm?MeetingID=786 on stem cell biology -- but stem cell researchers will need a few more bread crumbs before they can put this potentially exciting information to use. linkurl:Shinya Yamanaka;http://www.frontier.kyoto-u.ac.jp/rc02/kyojuE.html from Kyoto University and the Japan Science and Technology Agency presented a series of experiments designed to identify key reprogramming factors that convert a somatic cell into an embryonic one. Starting from a list of 100 proto-oncogenes and embryonic stem (ES) cell associated transcripts, or ECATs, he and his co-author winnowed the list to 24, then 10, then 4; all, when combined, appeared to induce pluripotency in murine embryonic MEF cells. (Below four factors, the authors were unable to obtain seemingly viable colonies.) The four factors also successfully reprogrammed fibroblasts from adult mice, and the authors plan to continue their work in human fibroblasts. This all sounded very exciting, until Yamanaka concluded his talk without naming the four seemingly crucial factors for reprogramming a somatic cell. A series of probing questions from the audience revealed a few details -- most are likely present in the oocyte, and may change the length of the cell cycle. He admitted that one factor is Oct4, which plays an important role in the maintenance of pluripotency, and is a key actor in much of the research presented during the conference. "I'm not brave enough to tell the other three," Yamanaka concluded.
Interested in reading more?

Become a Member of

The Scientist Logo
Receive full access to more than 35 years of archives, as well as TS Digest, digital editions of The Scientist, feature stories, and much more!
Already a member? Login Here

Meet the Author

Share
Illustration of a developing fetus surrounded by a clear fluid with a subtle yellow tinge, representing amniotic fluid.
January 2026, Issue 1

What Is the Amniotic Fluid Composed of?

The liquid world of fetal development provides a rich source of nutrition and protection tailored to meet the needs of the growing fetus.

View this Issue
Redefining Immunology Through Advanced Technologies

Redefining Immunology Through Advanced Technologies

Ensuring Regulatory Compliance in AAV Manufacturing with Analytical Ultracentrifugation

Ensuring Regulatory Compliance in AAV Manufacturing with Analytical Ultracentrifugation

Beckman Coulter Logo
Skip the Wait for Protein Stability Data with Aunty

Skip the Wait for Protein Stability Data with Aunty

Unchained Labs
Graphic of three DNA helices in various colors

An Automated DNA-to-Data Framework for Production-Scale Sequencing

illumina

Products

nuclera logo

Nuclera eProtein Discovery System installed at leading Universities in Taiwan

Brandtech Logo

BRANDTECH Scientific Introduces the Transferpette® pro Micropipette: A New Twist on Comfort and Control

Biotium Logo

Biotium Launches GlycoLiner™ Cell Surface Glycoprotein Labeling Kits for Rapid and Selective Cell Surface Imaging

Colorful abstract spiral dot pattern on a black background

Thermo Scientific X and S Series General Purpose Centrifuges

Thermo Fisher Logo