The Human Proteome > Testis

The testis-specific proteome

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Figure 1. The distribution of all genes across the five categories based on transcript abundance in testis as well as in all other tissues.

1980 genes show elevated expression in the testis compared to other tissues. The three categories of genes with elevated expression in testis compared to other organs are shown in Table 1.

Table 1. The genes with elevated expression in testis

The list of tissue enriched genes (n=1057) includes previously characterized genes with cellular location and functions well in-line with the function of the testis, as well as a large number of genes with unknown function and expression pattern.

Table 2. The 12 genes with the highest level of enriched expression in testis. "Predicted localization" shows the classification of each gene into three main classes: Secreted, Membrane, and Intracellular, where the latter consists of genes without any predicted membrane and secreted features. "mRNA (tissue)" shows the transcript level as FPKM values, TS-score (Tissue Specificity score) corresponds to the score calculated as the fold change to the second highest tissue.

Some of the proteins predicted to be membrane-spanning are intracellular, e.g., in the Golgi or mitochondrial membranes, and some of the proteins predicted to be secreted can potentially be retained in a compartment belonging to the secretory pathway, such as the ER, or remain attached to the outer face of the cell membrane by a GPI anchor.

The testis transcriptome

An analysis of the expression levels of each gene makes it possible to calculate the relative mRNA pool for each of the categories. The analysis shows that 79% of the mRNA molecules in the testis correspond to housekeeping genes and that only 15% of the mRNA pool corresponds to genes categorized to be testis enriched, group enriched, or testis enhanced. Thus, most of the transcriptional activity in the testis relates to proteins with presumed housekeeping functions as they are found in all tissues and cells analyzed.

Protein expression of genes elevated in testis

In-depth analysis of the highly enriched genes in testis using antibody-based protein profiling allowed us to create a map of where these proteins are expressed with regards to the various cell types in seminiferous ducts corresponding to the different phases of the spermatogenesis including spermatgonia, spermatocytes, spermatids and mature sperm as well as Sertoli cells and Leydig cells.

Proteins specifically expressed in spermatogonia

Spermatogonia are diploid cells that form the basal layer of the seminiferous duct and present the initial phase of the spermatogenesis. The spermatogonia can be divided into two subtypes, type A cells that have stem cell like properties and maintain the spermatogonia population and type B cells that produce primary spermatocytes.

Examples of genes expressed in spermatogonia include DMRT1, a transcription factor primarily expressed in the nuclei of spermatogonia that plays a key role in male sex determination and differentiation by controlling testis development and male germ cell proliferation, and the two genes PAGE1 and PASD1, two less well characterized proteins that belong to the group of cancer testis antigens.

Proteins specifically expressed in spermatocytes

Spermatocytes, derived from type B spermatogonia, can be subdivided into primary spermatocytes that enter the first meiosis and secondary spermatocytes that enter the second meiosis to produce haploid spermatids. Several of the testis specific proteins localized to spermatocytes are involved in testicular differentiation, proliferation and meiosis. Examples of genes specifically expressed in spermatocytes include DAZL, a well-known RNA binding protein that is essential for gametogenesis in both males and females and two poorly characterized genes TEX101 and SHCBP1L.

Proteins specifically expressed in spermatids

Spermatids are derived from secondary spermatocytes and these cells are subdivided into early, round spermatids that are transcriptionally active and late, elongated spermatids that are transcriptionally inert. The highly testis enriched proteins with known function and predominant expression in spermatids are for example involved in conversion of nucleosomal chromatin and sperm development and maturation. Examples of genes specifically expressed in spermatids include TNP1, which is involved in the conversion of nucleosomal chromatin to the compact, non-nucleosomal form found in the sperm nucleus and ACTL7B, a gene with only evidence of existence at the transcript level which encodes a putative protein of unknown function that is suggested to be a member of a family of actin-related proteins. The formation of the acrosome, a testis specific organelle required for sperm-egg interactions, is formed during the meiotic development of the late spermatid into mature spermatozoa. An example of a gene specifically expressed in the acrosome is ACRV1. This gene is expressed in the acrosomal vesicle during spermatogenesis and is associated with the acrosomal membranes and matrix of mature sperm. The ACRV1 protein 1 may be involved in sperm-zona binding or penetration.

Proteins specifically expressed in sperm

Following the maturation of late stage spermatids, the testicular end stage of spermatogenesis results in the formation of sperm. Sperm consists of uniflagellar sperm cells that are localized along the lumen of seminiferous ducts. Specific proteins localized to mature sperm are involved in functions including sperm motility and male fertility. Examples of genes specifically expressed in sperm include PRM2, a protamine whose function is to substitute for histones in sperm and package sperm DNA into a highly condensed, stable and inactive complex, GAPDHS, an enzyme that catalyzes an important energy-yielding step in carbohydrate metabolism during spermatogenesis and AKAP4, suggested to be a major structural component of sperm fibrous sheath, which also plays a role in sperm motility.

Proteins specifically expressed in Sertoli and Leydig cells

The interaction between germinal cells and Sertoli cells is essential both for the development of testis and for the progress of the spermatogenesis. Of the highly testis enriched genes in testis, only a few are specifically localized to Sertoli or Leydig cells as compared to the germ cell specific proteins. One example of a gene expressed in Sertoli cells is SLCO6A1 with currently only evidence at transcript level. The INSL3 gene, specifically expressed in Leydig cells, encodes for a well-known marker of Leydig cells, suggested to be involved in the development of urogenital tract and involved in intra-abdominal testicular descent.

Genes shared between testis and other tissues

There are 349 group-enriched genes expressed in the testis. Group enriched genes are defined as genes showing a 5-fold higher average level of mRNA expression in a group of 2-7 tissues, including testis, compared to all other tissues.

In order to illustrate the relation of testis tissue to other tissue types, a network plot was generated, displaying the number of commonly expressed genes between different tissue types.

Figure 2. An interactive network plot of the testis enriched and group enriched genes connected to their respective enriched tissues (grey circles). Red nodes represent the number of testis 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 3 tissues, but the resulting lists show the complete set of group enriched genes in the particular tissue.

The network plot reveals that most group-enriched genes are shared with the fallopian tube (n=139) and the tissue that testis shares second most genes with is the cerebral cortex (n=43).

A Gene Ontology (GO)-based analysis of the shared genes between testis and fallopian tube shows enrichment for genes related to cilia function and movement. One of the group enriched genes between testis and fallopian tube that is involved in cilia function and movement is DNAI1. This gene encodes a member of the dynein intermediate chain family and the encoded protein is part of the dynein complex in respiratory cilia.

For the shared genes between testis and cerebral cortex there is no clear pattern of enriched GO-terms. SH3GL3 is an example of a gene group enriched in testis and cerebral cortex and this gene is implicated in endocytosis.

Testis function

The main functions of the testis are spermatogenesis, which is production of haploid germ cells essential for reproduction, and synthesis of androgens (mainly testosterone) necessary for e.g development of male sex characteristics. These two functions occur in the two histologically different regions of the testis. Spermatogenesis takes place in seminiferous ducts whereas the production of androgens occurs in Leydig cells that are interspersed between the seminiferous ducts. During spermatogenesis, cells of seminiferous ducts undergo meiosis which contains several specific events such as reduction of the number of chromosomes, condensation of nucleus and removal of excess cytoplasm within the sperm. The sperm cells acquire unique morphological features and structures such as flagellum and acrosome that are necessary for sperm motility and fertilization of the egg.

Figure 3. A schematic figure representing the cross section of a seminiferous tubule illustrating the stepwise process of spermatogenesis . Initially immature cells, spermatogonia, located close to the basal membrane, divide by several rounds of mitosis into primary and secondary spermatocytes that divide by meiosis to form spermatids. The final step of spermatogenesis takes place in the lumen of the tubule where spermatids differentiate into haploid sperm.

Testis histology

The outermost part of the testis is surrounded by the tunica albuginea which is a fibrous layer of connective tissue. The testis is structured into lobules separated by fibrous septa where each lobule contains 1-4 seminiferous ducts. The seminiferous ducts make up the majority of the testicular tissue and each seminiferous duct consists of germ cells and Sertoli cells. Germ cells undergo mitosis and meiosis and mature into sperm in the process of spermatogenesis. Spermatogenesis involves several complex steps that can be morphologically determined and visualized in cross sections from seminiferous ducts. The different stages of spermatogenesis include undifferentiated spermatogonia in the basal compartment followed by more luminal mature spermatocytes and spermatids and the end product of this process which is mature sperm. The Sertoli cells are hormone producing non-dividing columnar cells that are attached to the basement membrane and exhibit cytoplasmic extensions around the germinal cells. Sertoli cells have irregular nuclei with a typical prominent nucleoleus. Interspread between the seminiferous ducts are the hormone-producing Leydig cells together with blood vessels, lymphatics, nerves and inflammatory cells.

The histology of human testis including detailed images and information about the different cell types can be viewed in the Protein Atlas Histology Dictionary.

Background

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

Transcript profiling and RNA-data analyses based on normal human tissues have been described previously (Fagerberg et al., 2013). Analyses of mRNA expression including over 99% of all human protein-coding genes was performed using deep RNA sequencing of 124 individual samples corresponding to 32 different human normal tissue types. RNA sequencing results of 7 fresh frozen tissues representing normal testis was compared to 117 other tissue samples corresponding to 31 tissue types, in order to determine genes with elevated expression in testis. A tissue-specific score, defined as the ratio between mRNA levels in testis compared to the mRNA levels in all other tissues, was used to divide the genes into different categories of expression. These categories include: genes with elevated expression in testis, genes expressed in all tissues, genes with a mixed expression pattern, genes not expressed in testis, and genes not expressed in any tissue. Genes with elevated expression in testis were further sub-categorized as i) genes with enriched expression in testis, ii) genes with group enriched expression including testis and iii) genes with enhanced expression in testis.

Human tissue samples used for protein and mRNA expression analyses were collected and handled in accordance with Swedish laws and regulation and obtained from the Department of Pathology, Uppsala University Hospital, Uppsala, Sweden as part of the sample collection governed by the Uppsala Biobank. All human tissue samples used in the present study were anonymized in accordance with approval and advisory report from the Uppsala Ethical Review Board.

Relevant links and publications

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

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

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

Djureinovic et al (2014). The human testis-specific proteome defined by transcriptomics and antibody-based profiling. Mol Hum Reprod.
PubMed: 24598113 DOI: 10.1093/molehr/gau018

Histology dictionary - testis