Transmembrane protein 151A


Transmembrane protein 151A, also known as TMEM151A, is a protein that is encoded by the TMEM151A gene.

Gene

The gene encoding transmembrane protein 151A is located on the positive strand of chromosome 11q13.2 and has two exons. The gene consists of a total of 2538 nucleotides, 1407 of which encode for the amino acids of the final transcript.

Protein

Transmembrane protein 151A has 468 amino acids, weighs 51,278 daltons, and is an integral component of cellular membranes. Transmembrane protein 151A has three transmembrane domains. The N-terminus of the protein is located in the cytosol and the C-terminus is located in the extracellular matrix. According to Compute pI, this protein has a molecular weight of approximately 51 kDa, which is the same molecular weight provided by NCBI protein. Sigma-Aldrich demonstrates that TMEM151A has a molecular weight of approximately 55 kDa which suggests that the protein may undergo post-translational modifications. The theoretical pI of the whole protein is approximately 8. Exon 1 is smaller and more acidic than exon 2. Transmembrane domain 2 is acidic, although it is located in exon 2 which averages to be basic. TMEM151A has no known isoforms, and is a part of family pfam15857 with one paralogue: TMEM151B.
The secondary structure of the protein is predicted to consist of approximately alpha helices and beta sheets but no coiled coils. Diagrams of the predicted tertiary structure and transmembrane domains are to the right.

Protein compositional analysis

The most abundant amino acids in TMEM151A are alanine and leucine. The least abundant are lysine, methionine, and asparagine. There is less asparagine, isoleucine, and lysine than would be expected for an average protein. The internal compositional analysis of all the individual segments of the protein all had amino acid abundances that fell into expected ranges except for the c-terminus. Specifically, there is less asparagine, isoleucine, and lysine and more arginine than would be expected for an average protein in the c-terminus. TMEM151A composition is highly conserved between mammals.

Protein level regulation

TMEM151A in Homo sapiens and other vertebrates have N-myristoylation sites in the N-terminus whereas non vertebrates instead have more phosphorylation sites instead in the N-terminus. TMEM151A in humans has 3 glycation sites, it may have a nuclear export signal, 2 palmoylation sites, many phosphorylation sites, 1 signal peptide, 1 arginine and lysine cleavage site, and multiple O-BetaGlcNac sites. The table below lists predicted post translational modifications for TMEM151A in several species.
Number of modificationsHumanUrsus arctos horribilisGallus gallusBranchiostoma floridaeCapitella teletaRamazzottius varieornatus
Palmoylation sites220122
Transmembrane regions333333
Phosphorylation sites*7437659995745381076
Sumo-interaction111004
Net glycation **33N/AN/AN/AN/A
Nuclear export signals332084
Phosphorylation sites92911297054102
Another prediction of transmembrane regions333333
Prediction of arginine and lysine cleavage sites110000
Signal peptide prediction110110
Sulfinated tyrosines221101
TMHMM transmembrane regions333333
O-beta glcnac attachment sitesmultiplemultiplemultiplemultiplemultiplemultiple

Cellular localization

TMEM151A protein is predicted to localize in the endoplasmic reticulum for Homo sapiens, mammals, lancelets, and some invertebrates. It is predicted to localize in the nucleus for birds and other invertebrates.
HumansUrsus arctos horribilisGallus gallusBranchiostoma floridaeCapitella teletaRamazzottius varieornatus
Endoplasmic reticulum55.639.14.355.666.713
Mitochondria22.230.417.411.108.7
Secretory system vesicles11.104.304.3
Plasma membrane11.1138.722.2034.8
Nuclear08.752.20017.4
Cytoplasmic08.78.7004.3
Extracellular004.3011.18.7
Vacuolar00011.111.10
Golgi000011.10

''Table 1: Predicted localization of TMEM151 in various species''

Gene level regulation

The TMEM151A promoter region consists of 1101 base pairs and it is directly adjacent to the base pairs which code for the first amino acid of the TMEM151A protein. Thousands of transcription factors were predicted to bind on this promoter region. Of those, 20 transcription factors are listed in the table below. Many transcription factors predicted to bind to the promoter region were related to the following categories:
  1. Neural and growth related
  2. Huntington's
  3. KRAB/Zinc finger
  4. Steroid
#Transcription factor descriptionMatrix similarity
1cAMP-responsive binding element1
2KRAB containing zinc finger protein1
3Huntington's disease gene regulatory region binding proteins 0.888
5EGR1, early growth response 10.906
6GA binding protein transcription factor, alpha
0.935
7ZF5 POZ domain zinc finger protein0.836
8ZF1-myeloid zinc finger 1 protein0.992
9Nerve growth factor induced protein C0.803
10Estrogen Receptor 20.914
11GATA-GATA binding factor 10.989
12Pleomorphic adenoma gene 1 1
13Glial cells missing homolog 10.953
14Androgene receptor binding site0.935
15EGR/nerve growth factor induced protein C & related factors0.902
16KRAB domain zinc finger protein 570.942
17Estrogen related receptors0.924
18Huntington's disease gene regulatory region binding proteins 0.850
19Leucine rich repeat interacting protein 10.865
20Krueppel-associated box-containing zinc-finger protein 57 0.960

Five different promoters influence the expression of this gene.

TMEM151A expression in humans

Immunohistochemistry demonstrates that TMEM151A RNA is primarily expressed in the brain, and has low levels of expression in the stomach, adipose tissue, retina, gallbladder, testes, colon, heart muscle, pancreas, salivary gland; a polyclonal rabbit TMEM151A antibody from Sigma Aldrich was used to get these results. These results were listed as “uncertain.”
Unigene microarray analysis shows that Homo sapiens TMEM151a DNA is found at relatively higher levels in the heart and the brain, and has lower levels of expression in multiple other tissues.

TMEM151A expression in other animals

Microarray analysis demonstrates that Mus musculus TMEM151a DNA has increased levels of expression in the heart, and has lower levels of expressions in multiple other tissues. Results from the Allen Brain Atlas demonstrate that the mouse isocortex has increased levels of in situ hybridization with TMEM151A. Microarray analysis of Canis lupus familiaris shows that TMEM151a DNA increased in both the cerebrum and the pancreas.

Homology and evolution

Transmembrane protein 151A has one paralogue: TMEM151B which has a 50.76% identity with TMEM151A. It is hypothesized that TMEM151A first arose as a gene duplicate of TMEM151B approximately 320 Million Years Ago in reptiles. TMEM151A is evolving at approximately the same rate as Hemoglobin B.
It appears as though TMEM151 is conserved in most if not all vertebrates, and is conserved in many invertebrates. The details of this conclusion are listed below:
TMEM151A and TMEM151B are conserved in all of the major mammal orders: Primates, Rodentia, Lagomorpha, Chiropetra, Artiodactyla, Carnivora, Soricomorpha, and Diprotodontia. TMEM151A and TMEM151B were present in the following reptile orders: Squamata and Testudinata. TMEM151B was found in many extant bird orders including: Columbiformes, Caprimulgiformes, Apodiformes, and Cuculiformes. TMEM151A was not present in any bird species. This suggests that TMEM151A evolved via gene duplication approximately 320 million years ago, as reptiles do have both TMEM151A and TMEM151B, but birds only have TMEM151A.
TMEM151B is present in the amphibian order Anura. TMEM151B could not be found in the amphibian order Caudata or Apoda in either BLAST or BLAT (bioinformatics). This absence in amphibians may be due to a lack of records or genetic divergence. TMEM151B is present in several bony fish orders including: perciformes, tetraodontiformes, and siluriformes. It could not be found in the bony fish order lophiiformes. TMEM151B is present in cartilaginous fishes, specifically sharks. TMEM151B was not found for lampreys or rays in BLAST; however, TMEM151B was found in BLAT for lampreys. This suggests that TMEM151B is likely found in many cartilaginous fishes; it is simply not recorded. TMEM151B could not be found in jawless fish in either BLAST or BLAT.
TMEM151B could not be found in tunicates, but it was found in one lancelet. As TMEM151B was found in lancelets, TMEM151B is found in Echinodermata, but not found in Porifera, nor Cnidaria. TMEM151B is also found in Annelida, Mollusca, Nematoda, Tardigrada, and Arthropoda'''.'''

Protein interactions

According to STRING, TMEM151A is predicted to interact with the following proteins:
  • TMEM71 – May localize in the mitochondrion or plasma membrane. It is primarily expressed in the circulatory and nervous system.
  • TMEM179-is located on chromosome 14, and or 90. It is predicted to localize in the mitochondria membrane
  • C9orf64 – this encodes the queosine salvage protein. Expression of this gene is highest in the duodenum and small intestine, it is a member of the DUF 2419 family.
  • C1orf167 – is a protein encoding gene of unknown function. It is associated with neural tube defects and folate sensitivity.
  • ZSCAN32 – is a human cervical cancer suppressor gene. It has RNA polymerase II specific activity
  • SAMD10 – stands for sterile alpha motif domain containing protein 10. It is located on chromosome 20. Diseases associated with this gene include retinitis pigmentosa. It is predicted to localize in the nucleus/nucleoplasm.
  • ANKDD1A – is located on chromosome 15 and is predicted to localize in the peroxisome and/or cytosol.
  • SOWAHD – Sosondowah Ankyrin repeat domain family member D. It is located on chromosome X and predicted to localize in the mitochondrion.
  • CCDC135 – is associated with diseases: Meckel syndrome, type 6 and type 1. It is located on chromosome 16 and is predicted to localize in the nucleus, cytosol, and most likely in the cytoskeleton.
  • TMEM88 – is located on chromosome 17 and is crucial for heart development and aids in the specification of lineage commitment of cardiomyocyte development

Research in humans

Illumina analysis has demonstrated that TMEM151A is one of 336 genes that may be used, in combination with the other genes, to diagnose colorectal cancer and/or the stage of that cancer. Specifically, TMEM151A is significantly upregulated in human monocytes circulating in the blood during colorectal cancer. TMEM151A is in linkage disequilibrium with gene CACNA1C; CACNA1C mutation is significantly associated with bipolar disorder p < 0.05. An unspecified variant of TMEM151A is one of 27 genes that has been associated with major depression disorder in Mexican Americans. These Mexican Americans experienced hyperactivation of the hypothalamic-pituitary-adrenal axis due to significant stress. Transplanted livers that came from deceased donors had a 4.83-fold upregulated expression of TMEM151A when compared to the expression levels of TMEM151A in livers that came from live donors.