We take our blood for granted, but its creation requires a complicated series of steps, starting with the formation of blood stem cells during early embryonic development, followed by progressive differentiation into the progenitors of red cells, white cells and platelets, and ultimately the full set of blood cells. Now, in the July 9 issue of Cell, researchers at Children's Hospital Boston report a surprising twist in how mature red blood cells form – which may explain the body's ability to rapidly replenish them in response to injury.
Previously, working with zebrafish – whose transparent bodies make it easy to watch blood formation -- the laboratory of Leonard Zon, MD, director of the Stem Cell Program at Children's, found a gene which, when mutated, left the embryonic fish bereft of red blood cells (this profoundly anemic strain was dubbed moonshine). Though the fish did form progenitors for red blood cells (called erythroid progenitors), these cells failed to become mature red blood cells, and instead died.
But why? The new research, led by Xiaoying Bai, PhD, in Zon's lab, showed that when the gene, TIF1 gamma, is mutated, the machinery that allows red blood cells to form from their progenitors is left in suspended animation.
In order for an erythroid progenitor to make a red blood cell, certain genes must be activated, or transcribed, to create templates for building the necessary proteins. Transcription involves an orchestrated series of events: tightly coiled DNA is unwrapped, unwound and its strands separated, then a portion of one strand is "read" down its length and used to make the template, cued by signals from the cell. But this reading process has been recently discovered to have built-in pauses, requiring another signal to tell transcription to resume.
TIF1 gamma, Bai and colleagues show, regulates this process of resuming transcription, known as transcriptional elongation. When TIF1 gamma is mutated in zebrafish, Bai and colleagues found, transcriptional elongation never happens. As a result, the erythroid progenitors get stuck in "pause" and never make mature red blood cells.
Further tests showed the same to be true in human cells – when erythroid progenitors were taken from patient blood samples and TIF1 gamma was blocked, red cells did not develop from them.
The pausing/stalling of transcription was once thought rare. But Bai, Zon and colleagues think it may provide a way for the body to quickly switch on production of red cells, and perhaps – since TIF1 gamma is found all over the body -- other kinds of cells the body needs to make quickly. Rather than have to laboriously set up all transcription each time red cells are needed, the machinery can simply be left on pause.
"We think this is the fastest way to respond to stimulation," says Bai. "The transcription machinery is already in place, but it's arrested until the right signal tells it to go. When you need massive production that needs to be synchronized to respond to the environment, this is the best way to regulate it."
Several recent genome-wide studies found a similar pausing/stalling to be common in the genome, suggesting it's a critical step in regulating gene activity. But this is one of the first studies to demonstrate a real-life application of stalling, in a live animal. "We think this is the first time anyone has shown genetically, and in vivo, that transcriptional elongation is involved in cell fate," says Bai.
The findings may have implications for treating severe anemia, as well as leukemia. In a form of leukemia known as MLL, there is evidence that transcription elongation factors are involved in oncogene formation, presumably overriding the "pause" mechanism and causing transcription to be stuck on – so white blood cells (leukocytes) are made over and over.
The study was supported by the National Institutes of Health and the Howard Hughes Medical Institute.
Children's Hospital Boston is home to the world's largest research enterprise based at a pediatric medical center, where its discoveries have benefited both children and adults since 1869. More than 1,100 scientists, including nine members of the National Academy of Sciences, 12 members of the Institute of Medicine and 13 members of the Howard Hughes Medical Institute comprise Children's research community. Founded as a 20-bed hospital for children, Children's Hospital Boston today is a 396-bed comprehensive center for pediatric and adolescent health care grounded in the values of excellence in patient care and sensitivity to the complex needs and diversity of children and families. Children's also is the primary pediatric teaching affiliate of Harvard Medical School. For more information about the hospital and its research visit: childrenshospital.org/newsroom.
Erin McColgan | EurekAlert!
New risk factors for anxiety disorders
24.02.2017 | Julius-Maximilians-Universität Würzburg
Stingless bees have their nests protected by soldiers
24.02.2017 | Johannes Gutenberg-Universität Mainz
In the field of nanoscience, an international team of physicists with participants from Konstanz has achieved a breakthrough in understanding heat transport
Cells need to repair damaged DNA in our genes to prevent the development of cancer and other diseases. Our cells therefore activate and send “repair-proteins”...
The Fraunhofer IWS Dresden and Technische Universität Dresden inaugurated their jointly operated Center for Additive Manufacturing Dresden (AMCD) with a festive ceremony on February 7, 2017. Scientists from various disciplines perform research on materials, additive manufacturing processes and innovative technologies, which build up components in a layer by layer process. This technology opens up new horizons for component design and combinations of functions. For example during fabrication, electrical conductors and sensors are already able to be additively manufactured into components. They provide information about stress conditions of a product during operation.
The 3D-printing technology, or additive manufacturing as it is often called, has long made the step out of scientific research laboratories into industrial...
Nature does amazing things with limited design materials. Grass, for example, can support its own weight, resist strong wind loads, and recover after being...
Nanometer-scale magnetic perforated grids could create new possibilities for computing. Together with international colleagues, scientists from the Helmholtz Zentrum Dresden-Rossendorf (HZDR) have shown how a cobalt grid can be reliably programmed at room temperature. In addition they discovered that for every hole ("antidot") three magnetic states can be configured. The results have been published in the journal "Scientific Reports".
Physicist Dr. Rantej Bali from the HZDR, together with scientists from Singapore and Australia, designed a special grid structure in a thin layer of cobalt in...
13.02.2017 | Event News
10.02.2017 | Event News
09.02.2017 | Event News
24.02.2017 | Life Sciences
24.02.2017 | Life Sciences
24.02.2017 | Trade Fair News