The Intestine-specific proteome

The Intestine transcriptome

Transcriptome analysis of the intestine can be visualized with regard to specificity and distribution of transcribed mRNA molecules (Figure 1). Specificity illustrates the number of genes with elevated or non-elevated expression in the intestine compared to other tissues. Elevated expression includes three subcategory types of elevated expression:

• Tissue enriched: At least four-fold higher mRNA level in intestine compared to any other tissues.
• Group enriched: At least four-fold higher average mRNA level in a group of 2-5 tissues compared to any other tissue.
• Tissue enhanced: At least four-fold higher mRNA level in intestine compared to the average level in all other tissues.

Distribution, on the other hand, visualizes how many genes that have, or do not have, detectable levels (NX≥1) of transcribed mRNA molecules in the intestine compared to other tissues. As evident in Table 1, all genes elevated in intestine are categorized as:

• Detected in single: Detected in a single tissue
• Detected in some: Detected in more than one but less than one third of tissues
• Detected in many: Detected in at least a third but not all tissues
• Detected in all: Detected in all tissues

Figure 1. (A) The distribution of all genes across the five categories based on transcript specificity in intestine as well as in all other tissues. (B) The distribution of all genes across the six categories, based on transcript detection (NX≥1) in intestine as well as in all other tissues.

As shown in Figure 1, 764 genes show some level of elevated expression in the intestine compared to other tissues. The three categories of genes with elevated expression in intestine compared to other organs are shown in Table 1. In Table 2, the 12 genes with the highest enrichment in intestine are defined.

Table 1. Number of genes in the subdivided categories of elevated expression in intestine.

Table 2. The 12 genes with the highest level of enriched expression in intestine. "Tissue distribution" describes the transcript detection (NX≥1) in intestine as well as in all other tissues. "mRNA (tissue)" shows the transcript level in intestine as NX values. "Tissue specificity score (TS)" corresponds to the fold-change between the expression level in intestine and the tissue with second highest expression level.

Protein expression of genes elevated in intestine

In-depth analysis of the elevated genes in intestine using antibody-based protein profiling allowed us to visualize the expression patterns of these proteins in different functional compartments including proteins involved in microvilli organisation and proteins involved in breakdown and uptake of nutrients.

Proteins involved in microvilli organization

Several genes with an elevated expression in the intestine encode proteins related to microvilli organization. (VIL1) is a calcium-regulated actin-binding protein that caps, severs as well as bundles actin filaments in the intestinal brush border. Microvilli are attached to each other via heterophilic complexes between (CDHR2) and (CDHR5). Thereby controlling the packing of the microvilli at the apical membrane.

VIL1
CDHR2
CDHR5

Proteins involved in digestion

The intestine is responsible for the uptake of many different dietary nutrients like fatty acids, amino acids and carbohydrates. Fatty acid uptake, metabolism and transport is facilitated by fatty acid binding proteins (FABP). For example, FABP2 is thought to be involved in triglyceride-rich lipoprotein synthesis. Complex carbohydrates like starch on the other hand are broken down by SI which is localized on the intestinal brush border. Simple carbohydrates get transported across the luminal membrane via SLC5A1, a sodium-dependent glucose transporter. For glucose and galactose SLC5A1 is the main transporter, mutations in this gene have been associated with glucose-galactose malabsorption.

FABP2
SI
SLC5A1

Genes shared between intestine and other tissues

There are 200 group enriched genes expressed in intestine. Group enriched genes are defined as genes showing a 4-fold higher average level of mRNA expression in a group of 2-5 tissues, including intestine, compared to all other tissues.

In order to illustrate the relation of intestine tissue to other tissue types, a network plot was generated, displaying the number of genes with shared expression between different tissue types.

Figure 2. An interactive network plot of the intestine enriched and group enriched genes connected to their respective enriched tissues (grey circles). Red nodes represent the number of intestine enriched genes and orange nodes represent the number of genes that are group enriched. The sizes of the red and orange nodes are related to the number of genes displayed within the node. Each node is clickable and results in a list of all enriched genes connected to the highlighted edges. The network is limited to group enriched genes in combinations of up to 2 tissues, but the resulting lists show the complete set of group enriched genes in the particular tissue.

Intestine shares most group enriched gene expression with the liver. One example of a gene expressed in both intestine and liver is SLC2A2, a membrane protein that is involved in the bidirectional transport of glucose. Another protein found in both organs is NPC1L1, a transporter capable of transporting free cholesterol as well as Vitamin E via vesicular endocytosis. The open reading frame C6orf58 is thought to be involved in early liver development, however the function is unknown. C6orf58 is expressed in the submucosa Brunner's glands in the duodenum, stomach and salivary gland. The intestinal tract also shares expression of several genes with the kidney. The enzyme DDC is expressed in the kidney and intestine, removes carboxyl groups of the precursors for dopamine, serotonin and tryptamine molecules.

SLC2A2 - duodenum
SLC2A2 - small intestine
SLC2A2 - liver

NPC1L1 - duodenum
NPC1L1 - small intestine
NPC1L1 - liver

C6orf58 - duodenum
C6orf58 - stomach
C6orf58 - salivary gland

DDC - duodenum
DDC - small intestine
DDC - kidney

Duodenum histology

The most proximal and widest part of the small intestine is the duodenum. It starts at the pylorus of the stomach, ends at the duodenojejunal junction and measures about 25 cm long. It receives partly digested food (chyme) from the stomach and bile and pancreatic fluids from the pancreaticobiliary duct. After entering the duodenum the acidic contents from the stomach is neutralized by secretion from the intestine and pancreas. Enzymes secreted from the pancreas initiate the degradation of lipids, carbohydrates and proteins to enable absorption.

As in all of the intestine, the mucosa forms finger-like projections called villi that extend into the intestinal lumen. These are epithelial folds lined by two types of cells, enterocytes and goblet cells. Enterocytes are simple columnar cells with basal elongated nuclei and an apical brush border. The brush border is the microscopic representation of small protrusions of the cell membrane, microvilli, which greatly increase the surface area of the cell enhancing absorptive capacity. The other cell type is mucus-secreting goblet cells that can be recognized by the presence of an apical mucous cup. The core of the villus is part of the lamina propria. The most numerous cells in the lamina propria are immune cells, most of which are lymphocytes. Because villi are the site of absorption of nutrition they have a rich blood supply, each villus is supplied by central arterioles and drained by central venules and a central lymph vessel.

Underlying the villi are the intestinal glands, also called the crypts of Lieberkuhn. These glands are lined with numerous relatively undifferentiated columnar cells that usually undergo two rounds of mitosis before differentiating into either absorptive cells or goblet cells. Enterocytes, goblet cells, paneth cells that secrete antibacterial enzymes (recognized by eosinophilic granules in their apical cytoplasm) and enteroendocrine cells also line the crypt. A thin layer of smooth muscle marks the end of the mucosa, the muscularis mucosae. In the submucosa there are numerous pale stained glands present, namely Brunner's glands. These are branched tubular or alveotubular glands lined with columnar secretory epithelium. They secrete large amounts of alkaline mucous that neutralize the acidic contents from the stomach.

The histology of human duodenum including detailed images and information can be viewed in the Protein Atlas Histology Dictionary.

Small intestine histology

The small intestine (jejunum and ileum) measures about 6 meters and absorbs nutrition, water and electrolytes. It is similar to the duodenum in histology and composition. The permanent transverse submucosal fold extending into the lumen of the intestine are termed plica circularis. The plica circularis consist of mucosa as well as submucosa. The core is the submucosa composed of loose connective tissue, blood vessels, nerves and dispersed lymphoid tissue. A distinctive feature of the jejunum and ileum is the lack of glands in the submucosa.

The mucosa is characterized by numerous finger-like villi that protrude into the lumen of the intestine. Enterocytes, which are columnar epithelial cells with basally located oval nuclei and an apical brush borderline the villi. The enterocytes located to the villi have mainly absorptive function. Interspersed between the enterocytes are goblet cells, which are recognized by their content of a large mucous globule, resembling a small "empty bubble" within the epithelial lining. The goblet cells are connected to the basement membrane by a thin, cytoplasmic strand that is difficult to distinguish in hematoxylin and eosin staining. Underlying the intestinal villi are the intestinal glands. They are straight tubular glands that are slightly dilated at their bottom. Intestinal stem cells line the proximal part of the glands. The stem cells give rise to all the cells in the epithelium, which are the paneth cells, the enterocytes, the goblet cells and the enteroendocrine cells. The paneth cells secrete antibacterial enzymes and are located in the lower portion of the intestinal glands. Paneth cells are recognized by eosinophilic granules in the cytoplasm.

The histology of human small intestine including detailed images and information can be viewed in the Protein Atlas Histology Dictionary.

Colon histology

The colon is divided into four parts, the ascending, transverse, descending and sigmoid colon is on average 1.5 meters long. Its main function is the reassertion of fluid, electrolytes, and vitamins. Since the colon has no villi or plica circularis the mucosa is smooth. Simple tubular intestinal glands (crypts of Lieberkuhn) extend through the entire thickness of the mucosa. The surface columnar epithelium and the cells lining the crypts are enterocytes, with an oval basal nucleus and apical brush border, the microscopic representation of microvilli. There are also numerous mucous secreting goblet cells recognized by their content of a large mucous globule. The lamina propria with connective tissue and inflammatory cells surround the crypts. A thin smooth muscular layer, the lamina muscularis mucosae marks the border between the mucosa and submucosa. The submucosa consists of loose connective tissue with vessels and nerves. Some solitary lymph follicles are also seen. The muscular layer (muscularis externa) consists of an inner circular smooth muscle layer, the outer longitudinal muscle layer is not continuous as in the rest of the gastrointestinal tract. It is divided into three thickened muscular bands, called teniae coli.

The histology of human colon including detailed images and information can be viewed in the Protein Atlas Histology Dictionary.

Background

Here, the protein-coding genes expressed in intestine are described and characterized, together with examples of immunohistochemically stained tissue sections that visualize corresponding protein expression patterns of genes with elevated expression in intestine.

Transcript profiling was based on a combination of three transcriptomics datasets (HPA, GTEx and FANTOM5), corresponding to a total of 9332 samples from 113 different human normal tissue types. The final consensus normalized expression (NX) value for each tissue type was used for classification of all genes according to the tissue specific expression into two different categories, based on specificity or distribution.

Relevant links and publications

Uhlén M et al., Tissue-based map of the human proteome. Science (2015)
PubMed: 25613900 DOI: 10.1126/science.1260419

Yu NY et al., Complementing tissue characterization by integrating transcriptome profiling from the Human Protein Atlas and from the FANTOM5 consortium. Nucleic Acids Res. (2015)
PubMed: 26117540 DOI: 10.1093/nar/gkv608

Fagerberg L et al., Analysis of the human tissue-specific expression by genome-wide integration of transcriptomics and antibody-based proteomics. Mol Cell Proteomics. (2014)
PubMed: 24309898 DOI: 10.1074/mcp.M113.035600

Gremel G et al., The human gastrointestinal tract-specific transcriptome and proteome as defined by RNA sequencing and antibody-based profiling. J Gastroenterol. (2014)
PubMed: 24789573 DOI: 10.1007/s00535-014-0958-7

Histology dictionary