Thesis/presentation.mkdn

---
title: Bioinformatic analysis of complex, high-throughput genomic and epigenomic data in the context of $\mathsf{CD4}^{+}$ T-cell differentiation and diagnosis and treatment of transplant rejection
author: |
    Ryan C. Thompson \
    Su Lab \
    The Scripps Research Institute
date: October 24, 2019
theme: Boadilla
aspectratio: 169
fontsize: 14pt
---

## Organ transplants are a life-saving treatment

::: incremental

* 36,528 transplants performed in the USA in 2018[^organdonor]

* 100 transplants every day!

* Over 113,000 people on the national transplant waiting list as of
  July 2019

:::

[^organdonor]: [organdonor.gov](https://www.organdonor.gov/statistics-stories/statistics.html)

## Organ donation statistics for the USA in 2018[^organdonor]

\centering

![](graphics/presentation/transplants-organ-CROP.pdf)

## Types of grafts

A graft is categorized based on the relationship between donor and recipient:

. . .

::: incremental

* **Autograft:** Donor and recipient are the *same individual*

* **Allograft:** Donor and recipient are *different individuals* of
  the *same species*

* **Xenograft:** Donor and recipient are *different species*

:::

## Recipient T-cells reject allogenic MHCs

:::::::::: {.columns}

::: {.column width="55%"}

:::: incremental

<!-- Vertical alignment hacks -->

\rule{\linewidth}{0pt}

\vspace*{12pt}

* TCR binds to both antigen *and* MHC surface \vspace{10pt}

* HLA genes encoding MHC proteins are highly polymorphic \vspace{10pt}

* Variants in donor MHC can trigger the same T-cell response as a
  foreign antigen

\vspace*{12pt}

\rule{\linewidth}{0pt}

::::

:::

::: {.column width="40%"}
<!-- ![\footnotesize Janeway's Immunobio- logy (2012), Fig. 9.19](graphics/presentation/janeway-fig9.19-TCR.png){ height=70% } -->
![TCR binding to self (right) and allogenic (left) MHC\footnotemark](graphics/presentation/tcr_mhc.jpg){ height=70% }
:::

::::::::::

\footnotetext[3]{\href{https://doi.org/10.1016/j.cell.2007.01.048}{Colf, Bankovich, et al. "How a Single T Cell Receptor Recognizes Both Self and Foreign MHC". In: Cell (2007)}}

## Allograft rejection is a major long-term problem

![Kidney allograft survival rates in children by transplant year[^kim-marks]](graphics/presentation/kidney-graft-survival.png){ height=65% }

[^kim-marks]: [Kim & Marks. "Long-term outcomes of children after solid organ transplantation". In: Clinics (2014)](https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3884158/?report=classic)

## Rejection is treated with immune suppressive drugs

<!-- TODO: Need a graphic, or maybe a table of common drugs +
mechanisms, or a diagram for periodic checking. -->

::: incremental

* Graft recipient must take immune suppressive drugs indefinitely

* Graft is monitored for rejection and dosage adjusted over time

* Immune suppression is a delicate balance: too much and too little
  are both problematic.

:::

## My thesis topics

<!-- TODO: Needs revision -->

### Topic 1: Immune memory
Genome-wide epigenetic analysis of H3K4 and H3K27 methylation in naïve
and memory $\mathsf{CD4}^{+}$ T-cell activation

### Topic 2: Diagnostics for rejection
Improving array-based diagnostics for transplant rejection by
optimizing data preprocessing

### Topic 3: Blood profiling during treatment
Globin-blocking for more effective blood RNA-seq analysis in primate
animal model for experimental graft rejection treatment

## Today's focus

### \Large Topic 1: Immune memory

\Large

Genome-wide epigenetic analysis of H3K4 and H3K27 methylation in naïve
and memory $\mathsf{CD4}^{+}$ T-cell activation

## Memory cells: faster, stronger, and more independent

![Naïve T-cell activated by APC](graphics/presentation/T-cells-A-SVG.png)

## Memory cells: faster, stronger, and more independent

![Naïve T-cell differentiates and proliferates into effector T-cells](graphics/presentation/T-cells-B-SVG.png)

## Memory cells: faster, stronger, and more independent

![Post-infection, some effectors cells remain as memory cells](graphics/presentation/T-cells-C-SVG.png)

## Memory cells: faster, stronger, and more independent

![Memory T-cells respond more strongly to activation](graphics/presentation/T-cells-D-SVG.png)

::: notes

Compared to naïve cells, memory cells:

* respond to a lower antigen concentration
* respond more strongly at any given antigen concentration
* require less co-stimulation
* are somewhat independent of some types of co-stimulation required by
  naïve cells
* evolve over time to respond even more strongly to their antigen

Result:

\normalsize

* Memory cells require progressively higher doses of immune suppresive
  drugs
* Dosage cannot be increased indefinitely without compromising the
  immune system's ability to fight infection

:::

## We need a better understanding of immune memory

* Cell surface markers fairly well-characterized

* But internal mechanisms poorly understood
  
. . .

\vfill

\large

**Hypothesis:** Epigenetic regulation of gene expression through
histone modification is involved in $\mathsf{CD4}^{+}$ T-cell
activation and memory.
  
## Experimental design

* Separately isolate naïve and memory $\mathsf{CD4}^{+}$ T-cells from
  4 donors
* Activate with CD3/CD28 beads
* Take samples at 4 time points: Day 0 (pre-activation), Day 1 (early
  activation), Day 5 (peak activation), and Day 14 (post-activation)
* Do RNA-seq + ChIP-seq for 3 histone marks (H3K4me2, H3K4me3, &
  H3K27me3) for each sample.

Data generated by Sarah Lamere, published in GEO as
[GSE73214](https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE73214)

## Time points capture phases of immune response

\centering

![](graphics/presentation/immune-response.png)<!-- { height=75% } -->

## Why study these histone marks?

::: incremental

* **H3K4me3:** "activating" mark associated with active transcription

* **H3K4me2:** Correlated with H3K4me3, hypothesized as a "poised" state

* **H3K27me3:** "repressive" mark associated with inactive 

* All 3 involved in T-cell differentiation, but activation dynamics
  unexplored

:::

## ChIP-seq sequences DNA bound to marked histones[^chipseq]

\centering

![](graphics/presentation/NRG-chipseq.png){ height=70% }

[^chipseq]: [Furey. "ChIP-seq and beyond: New and improved methodologies to detect and characterize protein-DNA interactions". In: Nature Reviews Genetics (2012)](http://www.nature.com/articles/nrg3306)

## A few intermediate analysis steps are required

![Flowchart of workflow for data analysis](graphics/CD4-csaw/rulegraphs/rulegraph-all-RASTER100.png)

## Histone modifications occur on consecutive histones

![ChIP-seq coverage in IL2 gene[^lamerethesis]](graphics/presentation/LaMere-thesis-fig3.9-SVG-CROP.png){ height=65% }

[^lamerethesis]: Sarah LaMere. "Dynamic epigenetic regulation of CD4 T cell activation and memory formation". PhD thesis. TSRI, 2015.

## Histone modifications occur on consecutive histones

![Strand cross-correlation plots](graphics/presentation/CCF-plots-A-SVG.png)

## Histone modifications occur on consecutive histones

![Strand cross-correlation plots](graphics/presentation/CCF-plots-B-SVG.png)

## Histone modifications occur on consecutive histones

![Strand cross-correlation plots](graphics/presentation/CCF-plots-C-SVG.png)

## SICER identifies enriched regions across the genome

![Finding "islands" of coverage with SICER[^sicer]](graphics/presentation/SICER-fig1-SVG.png)

[^sicer]: [Zang et al. “A clustering approach for identification of enriched domains from histone modification ChIP-Seq data”. In: Bioinformatics 25.15 (2009)](https://doi.org/10.1093/bioinformatics/btp340)

## IDR identifies *reproducible* enriched regions

![Example irreproducible discovery rate[^idr] score consistency plot](graphics/presentation/IDR-example-CROP-RASTER.png){ height=65% }

[^idr]: [Li et al. “Measuring reproducibility of high-throughput experiments”. In: AOAS (2011)](https://doi.org/10.1214/11-AOAS466)

## Finding enriched regions across the genome

![Peak-calling summary statistics](graphics/presentation/RCT-thesis-table2.2-SVG-CROP.png)

## Each histone mark has an "effective promoter radius"

![Enrichment of peaks near promoters](graphics/CD4-csaw/Promoter-Peak-Distance-Profile-PAGE1-CROP.pdf)

## Peaks in promoters correlate with gene expression

![Expression distributions of genes with and without promoter peaks](graphics/presentation/FPKM-by-Peak-Violin-Plots-A-SVG.png)

## Peaks in promoters correlate with gene expression

![Expression distributions of genes with and without promoter peaks](graphics/presentation/FPKM-by-Peak-Violin-Plots-B-SVG.png)

## Peaks in promoters correlate with gene expression

![Expression distributions of genes with and without promoter peaks](graphics/presentation/FPKM-by-Peak-Violin-Plots-C-SVG.png)

## Peaks in promoters correlate with gene expression

![Expression distributions of genes with and without promoter peaks](graphics/presentation/FPKM-by-Peak-Violin-Plots-D-SVG.png)

## Peaks in promoters correlate with gene expression

![Expression distributions of genes with and without promoter peaks](graphics/presentation/FPKM-by-Peak-Violin-Plots-Z-SVG.png)

## The story so far

<!-- TODO: Left column: text; right column: flip through relevant image -->

* H3K4me2, H3K4me3, and H3K27me3 occur on many consecutive histones in
  broad regions across the genome
* These enriched regions occur more commonly within a certain radius
  of gene promoters
* This "effective promoter radius" is consistent across all samples
  for a given histone mark, but differs between histone marks
* Presence or absence of a peak within this radius is correlated with
  gene expression
  
. . .

Next: Does the position of a histone modification within a gene
promoter matter to that gene's expression, or is it merely the
presence or absence anywhere within the promoter?
  
## H3K4me2 promoter neighborhood K-means clusters

![Cluster means for H3K4me2](graphics/CD4-csaw/ChIP-seq/H3K4me2-neighborhood-clusters-CROP.png)

## H3K4me2 promoter neighborhood cluster PCA

:::::::::: {.columns}
::: {.column width="50%"}
![Cluster means for H3K4me2](graphics/CD4-csaw/ChIP-seq/H3K4me2-neighborhood-clusters-CROP.png)
:::
::: {.column width="50%"}
![PCA plot of promoters](graphics/CD4-csaw/ChIP-seq/H3K4me2-neighborhood-PCA-CROP.png)
:::
::::::::::

## H3K4me2 promoter neighborhood cluster expression

:::::::::: {.columns}
::: {.column width="50%"}
![Cluster means for H3K4me2](graphics/CD4-csaw/ChIP-seq/H3K4me2-neighborhood-clusters-CROP.png)
:::
::: {.column width="50%"}
![Cluster expression distributions](graphics/CD4-csaw/ChIP-seq/H3K4me2-neighborhood-expression-CROP-ROT90.png)
:::
::::::::::

## H3K4me3 promoter neighborhood cluster PCA

:::::::::: {.columns}
::: {.column width="50%"}
![Cluster means for H3K4me3](graphics/CD4-csaw/ChIP-seq/H3K4me3-neighborhood-clusters-CROP.png)
:::
::: {.column width="50%"}
![PCA plot of promoters](graphics/CD4-csaw/ChIP-seq/H3K4me3-neighborhood-PCA-CROP.png)
:::
::::::::::

## H3K4me3 promoter neighborhood cluster expression

:::::::::: {.columns}
::: {.column width="50%"}
![Cluster means for H3K4me3](graphics/CD4-csaw/ChIP-seq/H3K4me3-neighborhood-clusters-CROP.png)
:::
::: {.column width="50%"}
![Cluster expression distributions](graphics/CD4-csaw/ChIP-seq/H3K4me3-neighborhood-expression-CROP-ROT90.png)
:::
::::::::::

## H3K27me3 promoter neighborhood cluster PCA

:::::::::: {.columns}
::: {.column width="50%"}
![Cluster means for H3K27me3](graphics/CD4-csaw/ChIP-seq/H3K27me3-neighborhood-clusters-CROP.png)
:::
::: {.column width="50%"}
![PCA plot of promoters](graphics/CD4-csaw/ChIP-seq/H3K27me3-neighborhood-PCA-CROP.png)
:::
::::::::::

## H3K27me3 promoter neighborhood cluster expression

:::::::::: {.columns}
::: {.column width="50%"}
![Cluster means for H3K27me3](graphics/CD4-csaw/ChIP-seq/H3K27me3-neighborhood-clusters-CROP.png)
:::
::: {.column width="50%"}
![Cluster expression distributions](graphics/CD4-csaw/ChIP-seq/H3K27me3-neighborhood-expression-CROP-ROT90.png)
:::
::::::::::

## What have we learned?

### H3K4me2 & H3K4me3

* Peak closer to promoter $\Rightarrow$ more likely gene is highly
  expressed
* Slightly asymmetric in favor of peaks downstream of TSS

. . .

### H3K27me3

* Depletion of H3K27me3 at TSS associated with elevated gene
  expression
* Enrichment of H3K27me3 upstream of TSS even more strongly associated
  with elevated expression
* Other coverage profiles not associated with elevated expression

## Differential modification disappears by Day 14

![Differential modification between naïve and memory samples at each time point](graphics/presentation/RCT-thesis-table2.4-A-SVG-CROP.png)

## Differential modification disappears by Day 14

![Differential modification between naïve and memory samples at each time point](graphics/presentation/RCT-thesis-table2.4-B-SVG-CROP.png)

## Convergence at Day 14 H3K4me2

![(Insert figure legend)](graphics/CD4-csaw/ChIP-seq/H3K4me2-promoter-PCA-group-CROP.png)

## Convergence at Day 14 H3K4me3

![(Insert figure legend)](graphics/CD4-csaw/ChIP-seq/H3K4me3-promoter-PCA-group-CROP.png)

## Convergence at Day 14 H3K27me3

![(Insert figure legend)](graphics/CD4-csaw/ChIP-seq/H3K27me3-promoter-PCA-group-CROP.png)

## Convergence at Day 14 RNA-seq (PC 2 & 3)

![(Insert figure legend)](graphics/CD4-csaw/RNA-seq/PCA-final-23-CROP.png)

## MOFA identifies shared variation across all 4 data sets

![(Insert figure legend)](graphics/presentation/MOFA-varExplained-matrix-A-CROP.png)

## MOFA identifies shared variation across all 4 data sets

![(Insert figure legend)](graphics/presentation/MOFA-varExplained-matrix-B-CROP.png)

## MOFA shared variation captures convergence pattern

![(Insert figure legend)](graphics/CD4-csaw/MOFA-LF-scatter-small.png)

## What have we learned?

* Almost no differential modification observed between naïve and
  memory at Day 14, despite plenty of differential modification at
  earlier time points.
* RNA-seq data and all 3 histone marks' ChIP-seq data all show
  "convergence" between naïve and memory by Day 14 in the first 2 or 3
  principal coordinates.
* MOFA captures this convergence pattern in one of the latent factors,
  indicating that this is a shared pattern across all 4 data sets.

<!-- ## Slide -->

<!-- ![(Insert figure legend)](graphics/CD4-csaw/LaMere2016_fig8.pdf) -->


## Takeaway 1: Each histone mark has an "effective promoter radius"

* H3K4me2, H3K4me3, and H3K27me3 ChIP-seq reads are enriched in broad
  regions across the genome, representing areas where the histone
  modification is present
* These enriched regions occur more commonly within a certain radius
  of gene promoters
* This "effective promoter radius" is specific to each histone mark
* Presence or absence of a peak within this radius is correlated with
  gene expression
  
## Takeaway 2: Peak position within the promoter is important

* H3K4me2 and H3K4me3 peaks are more strongly associated with elevated
  gene expression the closer they are to the TSS, with a slight bias
  toward downstream peaks.
* H3K27me3 depletion at the TSS and enrichement upstream are both
  associated with elevated expression, while other patterns are not.
* In all histone marks, position of modification within promoter
  appears to be an important factor in association with gene
  expression

## Takeaway 3: Expression & epigenetic state both converge at Day 14

* At Day 14, almost no differential modification observed between
  naïve and memory cells
* Naïve and memory converge visually in PCoA plots
* Convergence is a shared pattern of variation across all 3 histone
  marks and gene expression
* This is consistent with the hypothesis that the naïve cells have
  differentiated into a more memory-like phenotype by day 14.