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How the slime mould gets organised
The so-called cellular slime mould, a unicellular organism that may transition into a multicellular organism under stress, has just been found to have a tissue structure that was previously thought to exist only in more sophisticated animals. What's more, two proteins that are needed by the slime mould to form this structure are similar to those that perform the same function in more sophistical animals.
Shortly after an animal embryo forms, it develops a single layer of cells that, shaped like a hollow ball, is empty at its centre. Acting as a kind of 'man behind the curtain' that directs these cells to organise into this hollow formation are several proteins that help each cell touch its neighbours but keep its top surface exposed to the formation's empty interior.
Even after animals grow beyond the embryo stage, the cells in many organs of their bodies maintain this type of hollow structure. These organs include those in the digestive tracts of animals, which feature a layer of cells, called epithelial cells, that face inward to form a hollow structure and are shaped asymmetrically to give organs their directionality. For example, the asymmetric epithelial cells of animal intestines face inward to form a hollow structure through which nutrients are absorbed. Likewise, the asymmetric epithelial cells of animal glands, such as salivary and endocrine glands, also face inward to form a hollow structure. But instead of absorbing substances as do the epithelial cells of animal intestines, these glandular epithelial cells secrete into their hollow structure substances that they produce.
With funding from the National Science Foundation, Daniel Dickinson, W. James Nelson and William Weis - all of Stanford University - took a careful look at the final, mature stage of slime mould development under a high-powered microscope. They report their results in the journal Science, March 11, 2011.
The slime mould spends most of its life as a single-celled organism, living in soil and preying on bacteria. However when food runs short, thousands of slime mould cells aggregate to form a mound. They then grow into a fruiting body - which is a stalk, a few millimetres tall, whose top peeks over the surface of the ground and holds spores. The researchers found that the organisation and directionality of cells in this top part of the extending stalk are surprisingly similar to those of the epithelial cells of some organs of higher animals.
Dickinson and his colleagues also discovered that in order for the cells in the top of the slime mould's stalk to organise into an epithelium, they need analogues to two of the many proteins that are needed by animal cells to organise into an epithelium. Called alpha-catenin and beta-catenin, these slime mould analogues are genetically and biochemically similar to their animal versions. And when the researchers removed these analogues from the cells of slime moulds, they lost their ability to organise correctly.
In addition to requiring proteins that are similar to those required by some animal epithelial tissues, the slime mould's epithelium tissue behaves similarly to the epithelial tissue of some animals - it is secretory. It secretes proteins that coat the stalk of the fruiting body and give it the rigidity it needs to send its spores out onto the ground in search of new food.
'We don't know whether the ancient ancestor of slime moulds and animals was actually able to form an epithelium,' says Dickinson, 'but it must have had alpha-catenin and beta-catenin, and we suspect that these proteins had some role in organising cells.'
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