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Reconstructing the life history of a single cell

By R&D Editors | June 30, 2014

Researchers have developed new methods to trace the life history of individual cells back to their origins in the fertilized egg. By looking at the copy of the human genome present in healthy cells, they were able to build a picture of each cell’s development from the early embryo on its journey to become part of an adult organ.

During the life of an individual, all cells in the body develop mutations, known as somatic mutations, which are not inherited from parents or passed on to offspring. These somatic mutations carry a coded record of the lifetime experiences of each cell.

By looking at the numbers and types of mutations in a cell’s DNA, researchers were able to assess whether the cell had divided a few times or many times and detect the imprints, known as signatures, of the processes of DNA damage and repair that the cells had been exposed to during the life of the individual. Furthermore, comparing each cell’s mutations with those of other cells in the body enabled scientists to map out a detailed tree of development from the fertilized egg.

Reconstruction of early cell divisions of two mouse embryos: Each white-filled large circle represents an individual cell from a mouse embryo and the unique combination of mutations in its DNA. Each mutation is represented by a number and those highlighted in yellow were acquired in the most recent cell division. The smaller colour-filled circles are the final sets of cells taken from different parts of the mouse and there are an unknown number of cell generations between each set of cells and its closest identifiable precursor cell.“With this novel approach, we can peer back into an organism’s development,” says Dr. Sam Behjati, first author from the Wellcome Trust Sanger Institute. “If we can better understand how normal, healthy cells mutate as they divide over a person’s lifetime, we will gain a fundamental insight into what can be considered normal and how this differs from what we see in cancer cells.”

The team looked at mouse cells from the stomach, small bowel, large bowel and prostate. The single cells were grown to produce enough DNA to be sequenced accurately. Eventually, single-cell sequencing technology will develop so that this type of experiment can be conducted using just one cell. However, the tiny amounts of DNA in single cells mean that mutation data are not currently precise enough to reconstruct accurate lineages.

The researchers recorded differences in the numbers of mutations in cells from the different tissues studied, likely attributable to differences in rates of cell division. Moreover, different patterns of mutation were found in cells from different tissues, suggesting that they have been exposed to different processes of DNA damage and repair, reflecting different lifetime experiences.

This experiment used healthy mice. If mutation rates are similar in human cells, these techniques could be used to provide an insight into the life histories of normal human cells.

“The adult human body is composed of 100 million million cells, all of which have originated from a single fertilized egg,” says Professor Mike Stratton, senior author and Director of the Sanger Institute. “Much more extensive application of this approach will allow us to provide a clear picture of how adult cells have developed from the fertilised egg. Furthermore, by looking at the numbers and types of mutation in each cell we will be able to obtain a diary, writ in DNA, of what each healthy cell has experienced during its lifetime, and then explore how this changes in the range of human diseases.”

Genome sequencing of normal cells reveals developmental lineages and mutational processes

Source: Sanger Institute

 

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