A new genome for regeneration research
First complete genome assembly of planarian flatworm reveals treasure trove on the function and evolution of genes
A complete and fully assembled genome is critical for understanding the biological characteristics of an organism. Scientists have previously attempted to sequence the genome of Schmidtea mediterranea, but ended up with a collection of more than 100,000 short pieces. The reason for this is that a great deal of the genome consists of many, nearly identical copies of the same sequence that repeats over and over.
New sequencing methods
To overcome this challenge of an exceptionally repetitive genome, the research groups of Jochen Rink and Eugene Myers at the MPI-CBG utilized Pacific Bioscience’s long-read sequencing technology, operated at the DRESDEN-concept Sequencing Center, a joint operation between the MPI-CBG and the TU Dresden. This relatively new technology can directly “read” contiguous stretches of the genome up to 40,000 base pairs (or “letters”) long. Such long reads are dramatically more effective at bridging repetitive stretches in the genome than the more broadly used 100-500 base pair reads, thus resulting in up to 100-fold improvements in genome assembly statistics over previous assemblies.
Siegfried Schloissnig (HITS) was primarily responsible for developing a novel software system, called “Marvel”, that solves more of the jigsaw puzzle posed by the long-reads than previous such systems, and more efficiently. The assembly of the Schmidtea mediterranea genome involved eight terabytes of data that took the high-performance computing cluster at the HITS three weeks to complete.
But what can scientists actually do with the abundance of genetic information in a genome assembly? One of the surprises in the case of Schmidtea mediterranea was the likely absence of highly conserved genes such as MAD1 and MAD2. Both are present in nearly all other organisms because they fulfil a function in a checkpoint that ensures that both daughter cells get the same number of chromosomes after cell division. Yet despite the MAD1/2 gene loss, planarians retained the checkpoint function. How this is possible is one of the questions that the genome will help to answer. But Jochen Rink and his group are especially excited about using the genome assembly for understanding how planarians manage to regenerate from an arbitrary tissue piece. Rink explains: “We already know some of the genes required for regenerating a head, but now we can also search for the regulatory control sequences that activate the head genes only at the front end of a regenerating piece”. Further, the Rink group has assembled a large collection of planarian species from around the world, many of which have lost the ability to regenerate. “With a powerful toolbox for the assembly of difficult genomes now in place, we hope to soon use genome comparisons to understand why some animals regenerate, while so many do not. At least in the case of flatworms”, summarizes Rink.