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Unlocking Stem Cell, DNA Secrets To Speed Therapies

Date:
October 11, 2008
Source:
Florida State University
Summary:
Researchers have discovered that as embryonic stem cells turn into different cell types, there are dramatic corresponding changes to the order in which DNA is replicated and reorganized.

In mammalian nuclei, replication takes place at punctate sites or foci. Early-replicating foci localize to the interior of the nucleus (green), while the periphery of the nucleus and nucleoli harbor late replicating foci (red). Cytogenetic studies suggest very stable organization of the DNA within these labeled sites, but the molecular boundaries separating differentially replicating segments have remained elusive. High-resolution, microarray-based replication timing profiles (translucent graphs) revealed the sizes and locations of early- and late-replicating chromosome segments and demonstrated that they are highly conserved within a cell type, but globally re-organized and consolidated into larger coordinately replicating segments during differentiation of embryonic stem cells.
Credit: Courtesy of Florida State University Department of Biological Science

In a groundbreaking study led by a molecular biologist at Florida State University, researchers have discovered that as embryonic stem cells turn into different cell types, there are dramatic corresponding changes to the order in which DNA is replicated and reorganized.

The findings bridge a critical knowledge gap for stem cell biologists, enabling them to better understand the enormously complex process by which DNA is repackaged during differentiation -- when embryonic stem cells, jacks of all cellular trades, lose their anything-goes attitude and become masters of specialized functions.

As a result, scientists now are one significant step closer to the central goal of stem cell therapy, which is to successfully convert adult tissue back to an embryo-like state so that it can be used to regenerate or replace damaged tissue. Such therapies hold out hope of treatments or cures for cancer, Parkinson's disease, multiple sclerosis, spinal cord injuries and a host of other devastating disorders.

Using mouse and human embryonic stem cells, FSU researchers employed advanced imaging techniques and state-of-the-art genomics technology to demonstrate, with unprecedented resolution along long stretches of chromosomes, which sequences are replicated first, and which occur later in the process of differentiation.

"Understanding how replication works during embryonic stem cell differentiation gives us a molecular handle on how information is packaged in different types of cells in manners characteristic to each cell type," said David M. Gilbert, the study's principal investigator. "That handle will help us reverse the process in order to engineer different types of cells for use in disease therapies."

"We know that all the information (DNA) required to take on the identity of any tissue type is present in every cell, because we already can, albeit very inefficiently, create whole animals from adult tissue through cloning," Gilbert said. "We also can make a kind of artificial embryonic stem cells, called induced pluripotent stem cells, out of many adult cell types, but there are two major hurdles remaining. First, the methods currently used rely on the unnatural retroviral insertion of genes into patients' cells, and these genes are capable of forming tumors. Second, this method is very inefficient as well because only one in 1,000 cells into which the genes are inserted becomes pluripotent. We must learn how cells lose pluripotency in the first place so we can do a better job of reversing the process without risks to patients.

"The challenge is, adult cells are highly specialized and over the course of their family history over many generations they've made decisions to be certain cell types rather than others," he said. "In doing so, they have tucked away the information they no longer need on how to become other cell types. Hence, all cells contain the same genetic information in their DNA, but during differentiation they package it with proteins into 'chromatin' in characteristic ways that define each cell type. The rules that determine how cells package DNA are complicated and have been difficult for scientists to decipher."

But, Gilbert noted, one time that the cell "shows its cards" is during DNA replication.

"During this process, which was the focus of our FSU research, it's not just the DNA that replicates," he said. "All the packaging must be replicated as well in each cell division cycle."

He explained that embryonic stem cells have many more, smaller "domains" of organization than differentiated cells, and it is during differentiation that they consolidate information.

"In fact, 'domain consolidation' is what we call the novel concept we discovered," he said.

Gilbert likened the concept of domain consolidation to the undeclared or "undifferentiated" college student who then consolidates her literature resources during the course of declaring a major and specialization. "From a student with books on all subjects on all of her bookshelves comes a student who has placed all texts pertaining to her major on the eye-level shelf and moved the distantly-related, potentially distracting texts to the hard-to-reach bottom or top shelves," he said.

"Now, our challenge as scientists," said Gilbert, "is to build on what we've learned about domain consolidation so that we can efficiently and safely create patient-specific induced pluripotent stem cells or even coax the body's cells to change their specialization in response to medications."

Funding for the study came largely from grants awarded to Gilbert from the National Institutes of Health.

Paper co-authors from the FSU Department of Biological Science include postdoctoral assistants Ichiro Hiratani and Tomoki Yokochi and doctoral student Tyrone Ryba. Contributions also came from researchers at the Friedrich Miescher Institute for Biomedical Research in Basel, Switzerland; the University of Alabama at Birmingham Schools of Medicine and Dentistry; and the State University of New York, Upstate Medical University, Syracuse.


Story Source:

The above story is based on materials provided by Florida State University. Note: Materials may be edited for content and length.


Journal Reference:

  1. Hiratani et al. Global Reorganization of Replication Domains During Embryonic Stem Cell Differentiation. PLoS Biology, 2008; 6 (10): e245 DOI: 10.1371/journal.pbio.0060245

Cite This Page:

Florida State University. "Unlocking Stem Cell, DNA Secrets To Speed Therapies." ScienceDaily. ScienceDaily, 11 October 2008. <www.sciencedaily.com/releases/2008/10/081010154152.htm>.
Florida State University. (2008, October 11). Unlocking Stem Cell, DNA Secrets To Speed Therapies. ScienceDaily. Retrieved July 24, 2014 from www.sciencedaily.com/releases/2008/10/081010154152.htm
Florida State University. "Unlocking Stem Cell, DNA Secrets To Speed Therapies." ScienceDaily. www.sciencedaily.com/releases/2008/10/081010154152.htm (accessed July 24, 2014).

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