Recent strides in biotechnology have provided a wealth of information about the genomes of many species, some of which were challenging or impossible to interrogate with approaches that were dominating the field merely a few years ago.
As a result, unprecedented opportunities became available, including the possibility to perform genome-wide gene expression profiling and comparative genomic analyses, and to study changes that occur in specific states, such as during development, disease, or in response to environmental agents or therapeutic compounds.
Historically, many biological questions were addressed by relying on datasets that originated from large-scale gene expression studies. However, one of the shortcomings of this strategy is that gene expression heterogeneity, which is present even among genetically identical cells that are grown in the same culture or are found at the same developmental point, is obscured, and information about individual cells and cell-to-cell variability will only be captured by performing single-cell level analyses.
“The very next frontier for genomics, as a field, is single-cell genomics, and the expression profiling of single cells will likely be the next step,” says Jian-Bing Fan, Ph.D., senior director of scientific research at Illumina.
To gain information about transcriptional profiles at the single-cell level, investigators in Dr. Fan’s lab, in collaboration with researchers from the Karolinska Institute led by Sten Linnarsson, described a highly multiplexed genome-wide strategy using single-cell RNA-Seq.
In this protocol, ideally suited for single-cell analysis, 96 cells placed into the individual wells of a 96-well plate were simultaneously lysed. The mRNAs were converted to cDNAs, and after barcodes and primer binding sequences were introduced by the template-switching activity of reverse transcriptase, the cDNAs were pooled and processed for 5´-end sequencing on the Illumina next-gen sequencing platform. This technique can use as little as a few picograms of starting mRNA, and is appropriate for the transcriptional profiling of rare cells.
Dr. Fan, in a collaboration with Kun Zhang, Ph.D., at the University of California, San Diego, is currently developing a strategy to generate a high-resolution three-dimensional map of transcriptional activities in single cells. In the past, after being isolated, human tissue samples were trypsinized and the resulting cell suspensions were used to examine individual cells. But during this procedure, the spatial relationship among cells from the original tissue sample was lost.
“An important aspect of the technology that we are working on is the additional layer of information that it provides. It does not require prior knowledge about the identity of the specific cell types and will be fundamental for understanding cellular functions that shape development and disease,” says Dr. Fan.
While data analysis promises to be challenging, and might require the development of new types of protocols, a new level of spatial organization that has not been available before is about to emerge.
“Mapping the specific individual cells back to the three-dimensional organ or tissue is challenging, but this is the future direction into which single-cell gene expression profiling will develop,” explains Dr. Zhang.
High-Resolution 3D Map
Recently, particularly with the developments in the field of epigenetics, the interface between DNA methylation and gene expression has become a vibrant research topic. For many years, it has been known that genes can become switched off by abnormal methylation in cancer. Subsequently, studies that examined the methylome identified many genes that exhibit aberrant methylation in cancer cells, when compared to their untransformed counterparts.
“Most of these events are probably irrelevant and, in all likelihood, they represent the consequence of the cell being a cancer cell, just as it also happens with mutations, many of which are known to be passengers,” says Peter A. Jones, Ph.D., D.Sc., distinguished professor of urology and biochemistry at the University of Southern California.
While the presence of aberrant DNA methylation changes in cancer cells has become relatively easy to explore, a much more challenging aspect is to determine whether these methylation changes are driving the process of malignant transformation or whether their emergence is consequential to it. Dr. Jones and colleagues recently described an approach that facilitates the identification of the epigenetic driver events required for cancer survival.
The investigators hypothesized that the few key chromosomal regions whose methylation is required for cancer cell survival would preferentially remain methylated when global methylation levels are reduced. After surveying residual DNA methylation levels in cancer cells with genetically disrupted DNA methyltransferases and clustering profiles from normal cells and primary cancer tissues, Dr. Jones and colleagues used gene expression meta-analysis to define the regions that are dependent on DNA methylation-dependent gene silencing.
Their strategy helped identify a set of promoters whose methylation is required for somatic cancer cell survival. Some of the respective genes are shared among several tumor types, while others are cancer- or tissue- specific. “The genes identified by this approach have not been previously known as tumor suppressor genes,” notes Dr. Jones.
In addition to helping define and validate the minimal DNA methylation profile that is necessary and functionally relevant for cancer cell survival, this approach advances our knowledge on the molecular events that drive cancer development, and promises to define a new generation of epigenetic therapies, in which the alterations that are being targeted are exactly the ones that the cancer cells rely on for survival.
While over the past 15 years the field of DNA methylation has focused on promoters, there are additional regions where methylation, even though not well understood functionally, could play important biological roles.
“We are looking more globally to see whether the bodies of the genes and the enhancers, which also undergo methylation, but we do not know yet it role at these locations, is important. It is important to look beyond promoters,” says Dr. Jones.
A significant challenge in biomedical sciences emerged when functional genomics developments, which uncovered novel aspects about biological systems, have not been paralleled in pace by drug discovery advances.
“Another problem is that the current strategy of optimizing candidate therapeutic compounds, which relies on a single target, is somewhat dangerous, and measuring the collective response of all relevant genes related to a specific phenotype, which is a much better option, has been technologically challenging,” says Xiang-Dong Fu, Ph.D., professor of cellular and molecular medicine at the University of California, San Diego.
To address this challenge, Dr. Fu and colleagues recently developed and described RASL-Seq, a new massively parallel quantitative gene analysis strategy in which RNA-mediated oligonucleotide annealing, selection, and ligation are coupled with next-generation sequencing, allowing hundreds of genes to be followed concomitantly under thousands or tens of thousands of distinct conditions.
RASL-Seq helped investigators in Dr. Fu’s lab develop a high-throughput sequencing method, which allows multi-target drug design to be performed in a pathway-centric, high-throughput fashion, a strategy neatly designed for the study of small molecules that affect disease-specific gene expression pathways. The fact that specific drug targets do not need to be identified in advance represents one of its advantages over conventional chemical screening.
Dr. Fu and colleagues illustrated the power of this technique in a study that sought to identify small inhibitors of androgen receptor-mediated gene expression for treating hormone-refractory prostate cancer and identified several classes of compounds. One of them, a cardiac glycoside, inhibited both androgen-sensitive and androgen-resistant prostate cancers without exhibiting severe cytotoxicity, and this effect most likely occurred through the proteasome-dependent degradation and destabilization of the androgen receptor.
“This approach brings a unique advantage when studying complex diseases because of the multitude of pathways that are involved. It may contribute to an integrated pattern of gene expression,” explains Dr. Fu.
In another study using RASL-Seq, investigators in Dr. Fu’s lab blocked different branches of EGF-induced signaling and unveiled a serine/arginine protein-specific kinase (SRPK)-dependent signal transduction pathway with a central role in regulating alternative splicing in mammalian cells.
“This is an intriguing research area, because many diseases are known to be caused by defects in splicing regulators, but very few signaling molecules involved in regulated splicing have been characterized to date,” says Dr. Fu.
“In many diseases, even though we can identify the environmental input linked to pathogenesis, we do not know how it contributes to the pathological modifications,” notes Feng C. Zhou, Ph.D., professor of anatomy, cell biology and neurobiology at the Indiana University School of Medicine.