Genes' interplay gives clues to how new cell types could evolve

April 5, 2018, University of Bath
Loss of sox10 and sox5 genes results in complex changes in numbers of shiny leucophores in medaka fish. Upper fish shows a normal, wild-type medaka -- note the line of shiny leucophores along the midline. All other fish lack all function of Sox5 gene, but the bottom three show loss of increasing numbers of copies of Sox10 genes, with the bottom fish having neither Sox10 nor Sox5 function. Credit: Yusuke Nagao and Robert Kelsh

Developmental biologists at the University of Bath have gained insights into how a family of essential genes interact differently between different parts of the body and between species, which could offer clues about how new types of cells come to evolve.

The researchers from the Department of Biology & Biochemistry, working with colleagues from two Japanese universities, were interested in how an important family of regulatory genes called SOX genes affect cell development as zebrafish and medaka fish grow.

SOX genes are found in all animals, such as mammals (including humans), reptiles, birds, fish and insects , and are known to be crucial in the development of brain , stem cells and in various other types of specialised cell as they develop from their .

There are around 20 SOX genes which code for proteins called SOX transcription factors. These act to regulate when genes are switched on and off by attaching to DNA strands, controlling activity of the genes nearby.

Uncovering how these genes function has important consequences for understanding how the body makes different cell-types, and for diseases in which this fails. For example, SOX10 has long been associated with diseases in which melanocytes and neurons fail to be made, such as Waardenburg Syndrome and Hirschsprung Disease.

The team were interested in how the SOX proteins interacted when develop in these two fish species. Zebrafish have three types of cells called melanocytes, iridophores and xanthophores, while Medaka have the same three and an additional type called leucophores; together these cells form the important and often beautiful pigment patterns of these and other fish.

They studied two SOX proteins, encoded by the SOX10 and SOX5 , which are involved in pigment cell development in both species.

They discovered that across both species SOX10 is essential to develop the three types of pigment cells they have in common, and SOX5 slightly downregulated the action of SOX10 for all three types of pigment cell in zebrafish, and for melanocytes and iridophores in medaka.

However in medaka fish both SOX10 and SOX5 worked in a completely different way by co-operating to repress leucophore formation, and to promote the formation of xanthophores.

The research is published in PLOS Genetics.

Professor Robert Kelsh, who led the research at the University of Bath, said: "How individual cells become specific cell-types, from precursor cells that could become anything, is a fundamental question in developmental and .

"We have worked on SOX10 for a long-time, showing its important role in helping make many specialised cell-types. We began looking at the role for SOX5 because this gene has been shown to work with SOX10, but in different ways. Our research shows that these transcription factors are working in a context-specific way - in some cell-types they work together, in others SOX5 antagonises SOX10. For melanocytes this antagonism functions the same way as it does in mammals. But what really surprised us was how SOX5 and SOX10 interact in opposite ways to govern development of xanthophores.

"We see the same proteins are working together differently depending on the context - so what's happening? We suggest that this likely relates to the evolution of a novel pigment cell type - the reflective leucophore - in medaka. Our previous work had shown that at a genetic level we can consider the leucophore to be a xanthophore that has been modified to become reflective. We speculate that this may be intimately linked to the change in relationship between SOX5 and SOX10 in the formation of the xanthophore. But exactly why, and exactly how this works, we don't know - that is the next mystery for us to investigate!"

Explore further: Why stem cells don't just want to make neurons

More information: Distinct interactions of Sox5 and Sox10 in fate specification of pigment cells in medaka and zebrafish, PLOS Genetics (2018). journals.plos.org/plosgenetics … journal.pgen.1007260

Related Stories

Why stem cells don't just want to make neurons

April 1, 2011

Research being presented today at the UK National Stem Cell Network annual science conference provides another piece in the puzzle of why it can be so hard to produce large numbers of the same type of cell in the lab – ...

Errant gene turns cells into mobile cancer factories

September 10, 2015

A single stem cell has the potential to generate an animal made of millions of different types of cells. Some cancers contain stem-like but abnormal cells that can act like mini factories to rapidly churn out not only more ...

A guppy's spots formed by layers of color cells

January 22, 2014

At least three pigment cell types from multiple layers of skin contribute to the color patterns of male guppies, according to a study published in PLOS ONE on January 22, 2014 by Verena Kottler from the Max Planck Institute ...

Recommended for you

Team discovers a new take on early evolution of photosynthesis

April 24, 2018

A team of scientists from Arizona State University's School of Molecular Sciences has begun re-thinking the evolutionary history of photochemical reaction centers (RCs). Their analysis was recently published online in Photosynthesis ...

0 comments

Please sign in to add a comment. Registration is free, and takes less than a minute. Read more

Click here to reset your password.
Sign in to get notified via email when new comments are made.