October 22, 2015

Salk scientists discover protein factories hidden in human jumping genes

Researchers identify a new core element of primate jumping genes capable of producing previously unknown proteins

索尔克新闻


Salk scientists discover protein factories hidden in human jumping genes

LA JOLLA–Scientists have discovered a previously unknown wellspring of genetic diversity in humans, chimps and most other primates. This diversity arises from a new component of itinerant sections of genetic code known as jumping genes.

In a paper published October 22, 2015 in 细胞, Salk scientists report finding human and chimp DNA peppered with sequences of genetic code they’ve dubbed ORF0, which spreads throughout the genome on jumping genes. The ORF0 sequences may produce hundreds or even thousands of previously unknown proteins.

Salk researchers discovered a new genetic component, called ORF0, spread throughout the DNA of humans, chimps and most other primates. This image shows the locations of ORF0 on human and chimp chromosomes.

点击此处 用于高分辨率图像。.

图片:由萨克生物研究所提供

The abundance of ORF0 instances in the human genome suggests that it played–and still plays–an important role in evolutionary diversity and flexibility by serving as a mechanism for generating novel proteins. The discovery of these mobile protein factories may also shine light on the origins of genetic mutations responsible for cancer, mental disorders and other diseases.

“This discovery shows that jumping genes are an even more important source of variation in the primate genome than we thought, whether you’re looking at the level of different species, different people or even the different cells within an individual’s body,” says 鲁斯蒂·盖奇, senior author of the paper and a professor in Salk’s 遗传实验室.

With the sequencing of the human genome, it became clear that jumping genes–mobile genetic elements first discovered in maize by Barbara McClintock in the early 1950s–were also present and highly active during human evolution. About half of the human genome resulted from sequences of genetic code that moved or insert extra copies of themselves throughout the genome.

The evolutionary importance of jumping genes was highlighted by the results of another recent study by Gage and collaborators at Stanford. The research used stem cell technologies developed in Gage’s lab to explore how differences in gene expression contribute to human and chimp facial structure. The findings, also reported in Cell, suggested that jumping genes played a role in the evolutionary split between humans and other primates.

In the more recent study that uncovered ORF0, Gage and his colleagues focused on a class of jumping genes known as LINE-1 elements, which make up about 17 percent of the human genome. These elements contain all the necessary genetic machinery for moving themselves and other classes of jumping genes, unaided, to elsewhere in the genome.

Previously, it was thought that LINE-1 elements contain just two sequences that coded for proteins, the ultimate product of genes that serve a wide range of roles in our cells and organs. These sequences are known as open reading frames (ORF), and the two previously known sequences, ORF1 and ORF2, are thought to be involved in producing proteins that are important for allowing LINE-1 elements to move around in the genome.

Rusty Gage and Ahmet Denli

点击此处 用于高分辨率图像。.

图片:由萨克生物研究所提供

In their new study, Gage and his colleagues discovered a third open reading frame. They named it ORF0 based on its location in the LINE-1 element next to ORF1. The scientists found ORF0 in about 3,500 locations in the DNA of humans and about 3,000 locations in the chimp and most other primate genomes.

The structure of LINE-1 elements is such that when an element moves to another site there is a possibility that the ORF0 sequence can blend with genetic sequences in new location in DNA. The result of the new gene sequences can be a new protein. Evolutionarily speaking, this represents a way to generate entirely new molecules that could be beneficial to a species. On the other hand, the reshuffling of an existing ORF0 sequence during a jump could result in a disease-causing mutation.

“This discovery redraws the blueprint of an important piece of genetic machinery in primates, adding a completely new gear,” says Ahmet Denli, a staff scientist in Gage’s lab and the first author on the paper reporting the findings. “Jumping genes with ORF0 are basically protein factories with wheels, and over the eons evolution has been driving the bus.”

Now that they have identified ORF0 in the primate genome, Denli says they plan to determine how many of the instances of ORF0 actually code for proteins and to investigate what function those proteins serve.

The researchers also plan to investigate the behavior of ORF0 in different cell types and diseases. They are particularly interested in exploring its role in cancers and in neurological disorders such as schizophrenia, where previous studies have suggested jumping genes may be involved.

Other authors on the paper include Salk Institute researchers Iñigo Narvaiza, Bilal E. Kerman, Monique Pena, Christopher Benner, Maria C. N. Marchetto, Jolene K. Diedrich, Aaron Aslanian, Jiao Ma, James J. Moresco, Lynne Moore, 托尼·亨特艾伦·萨加特利安.

该研究得到了 Leona M. 和 Harry B. Helmsley 慈善信托基金, , 那个 JPB基金会 and the G. Harold and Leila Y. Mathers Charitable Foundation.

出版信息

日记

细胞

标题

Primate-Specific ORF0 Contributes to Retrotransposon-Mediated Diversity

作者

Ahmet M. Denli, Iñigo Narvaiza, Bilal E. Kerman, Monique Pena, Christopher Benner, Maria C.N. Marchetto, Jolene K. Diedrich, Aaron Aslanian, Jiao Ma, James J. Moresco, Lynne Moore, Tony Hunter, Alan Saghatelian, and Fred H. Gage

更多信息

宣传办公室
电话:(858) 453-4100
press@salk.edu

萨尔克生物学研究所

萨尔克研究所是一个独立的非营利性研究机构,由首个安全有效的脊髓灰质炎疫苗的研发者乔纳斯·索尔克于1960年创立。该研究所的使命是推动以合作、敢于冒险为特点的基础性研究,以应对癌症、阿尔茨海默病和农业脆弱性等社会最紧迫的挑战。这项基础科学支撑着所有的转化研究,产生有助于全球新药和创新的见解。.