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PRR29

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PRR29
Identifiers
AliasesPRR29, C17orf72, proline rich 29
External IDsMGI: 1922823; HomoloGene: 130357; GeneCards: PRR29; OMA:PRR29 - orthologs
Orthologs
SpeciesHumanMouse
Entrez

92340

75573

Ensembl

ENSG00000224383

ENSMUSG00000009210

UniProt

P0C7W0

B1ARI9

RefSeq (mRNA)

NM_001164257
NM_001191029
NM_001191030
NM_001191031

NM_029345

RefSeq (protein)

NP_001157729
NP_001177958
NP_001177959
NP_001177960

NP_083621

Location (UCSC)Chr 17: 64 – 64 MbChr 11: 106.26 – 106.27 Mb
PubMed search[3][4]
Wikidata
View/Edit HumanView/Edit Mouse
Proline-Rich Protein 29
Identifiers
SymbolPRR29
Alt. symbolsC17orf72
Alt. namesChromosome 17 Open Reading Frame 72
NCBI gene92340
RefSeqNM_001164257.2
UniProtP0C7W0
Other data
LocusChr. 17 q23
Search for
StructuresSwiss-model
DomainsInterPro

PRR29 (proline-rich protein 29) is a protein encoded by the PRR29 gene located in humans on chromosome 17 at 17q23.[5][6][7]

Its function is not fully understood. Its name is derived from the chain of 5 proline amino acids located toward the end of the protein. The primary domain within the sequence of this protein is known as DUF4587.[5] It is reported to have high levels of expression in tissues pertaining to the circulatory system and the immune system.[8] It is hypothesized that PRR29 is a nuclear protein that facilitates communication between the nucleus and the mitochondria.

The gene is also commonly known as C17orf72. The gene has a size of 5961 base pairs and contains five exons.[6]

Gene

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Location of PRR29 gene relative to its neighbors

PRR29 is located on the long arm of chromosome 17 (17q23.3), starting at 63998344 and ending at 64004305.[6] The gene spans 5961 base pairs and is oriented on the plus strand. Genes SNHG25 and LOC105371858 neighbor PRR29 on chromosome 17.The gene ICAM2 is located on the negative strand, directly opposite of PRR29.

The human gene for PRR29, also referred to as C17of72, spans 6 exons and is located at the genomic coordinates chr17:63,998,351-64,002,516 on the positive DNA strand (hg38). It is 4,166 base pairs in length including introns. After they have been removed, the length is shortened to 3,611 base pairs.[9]

mRNA

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The gene has 12 common splice variants and one unspliced form.[10] The longest transcribed mRNA is made up of 3048 base pairs and the transcribed protein sequence for this mRNA is 189 amino acids.[6]

Locus of PRR29[11]
Genomic view of PRR29

Protein

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General properties

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Homo sapiens PRR29 has several protein isoforms, with the longest being 236 amino acids.[6] PRR29 has a predicted Isoelectric point of 5.23 and a predicted Molecular weight of 26.1 kilodaltons. PRR29 is characterized by a larger than average proportion of prolines (19.1%) and a smaller than average amount of asparagines (0.4%)[12]

The PRR29 protein is estimated to have a molecular weight of 20.7 kDa. Its isoelectric point is predicted to lie at 4.83.[13]

Domains

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PRR29 contains a proline rich region within its sequence from amino acids 73 to 166. A domain of unknown function, DUF 4587, is also present from amino acids 39 to 112 or 113.[14][15] DUF 4587 is usually between 64 and 79 amino acids long and contains the two sequence motifs QNAQ and HHH. PRR29 is predicted to contain multiple alpha helix and beta-sheet forming regions. Specifically, the DUF 4587 region is predicted to form an alpha helix.[16]

It contains one proline-rich region motif that extends from amino acid 39 to 107.[17]

Secondary and Tertiary Structure

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3D structure of PRR29 protein

The secondary structure is characterized by high confidence in the presence of an alpha helix from amino acid 43 to 70 with the rest consisting of coils.[18] In terms of tertiary structure, predictive tools returned low confidence in all sections of the protein besides the core alpha helix.[19]

Untranslated Regions

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The secondary structure of the 5' UTR of PRR29 consists of a singular stem-loop that is almost wholly conserved between orthologs. The 3' UTR is much longer, containing 41 different stem loops in its secondary structure. Any predicted miRNA binding to PRR29 is believed to be nonfunctional.[20]

Subcellular localization

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Using PSORTII, PRR29 is predicted to localize in the nucleus of the cell.[21] PSORTII does not predict any targeting sequences or signal peptides. Data on localization of PRR29 within cells shows that it is primarily found in the nucleus, followed by the mitochondria and cytoplasm.[22]

Post-Translational Modification

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PRR29 is predicted to undergo sumoylation, acetylation, and serine, threonine and tyrosine phosphorylation.[23] The most common types of post-translational modification that occur for this protein are phosphorylation, glycosylation, hydroxylation, and sumoylation.[24] They contribute to the stability, structure, and folding of the protein.

Interactions

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The interactome of PRR29 is not yet well characterized. One experimental study found that a Sus scrofa PRR29-like protein interacts with the N-terminal protease of classical swine fever virus (CSFV).[25]

3D structure prediction from I-TASSER [26]

Expression

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Expression data for PRR29 based on RNA sequencing of human tissue samples
Expression data for PRR29 from Illumina bodyMap 2 transcriptome

PRR29 is ubiquitously expressed throughout the body. However, there is particularly high expression in the ovaries, muscle, heart, testes, and thymus.[27] According to PaxDb, PRR29 abundance falls in the bottom 5% relative to other proteins.[28]

Its expression is concentrated in related tissues including the spleen, lungs, white blood cells, and heart.[8] In situ hybridization data reveals that expression in the human brain is brain is relatively low in the forebrain but higher in the basal ganglia, midbrain, and hindbrain with the exception of the cerebellar cortex. For comparison, expression in the mouse brain is focused in the isocortex, olfactory region, hippocampus, cortical subplate, and cerebellum.

Transcript-Level Regulation

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Prediction of transcription factors that bind to the promoter region for PRR29 include ones involved with the activation of leukocytes and the formation of blood cells.[29] Abundance of the protein relative to others found in the human body is currently unknown.[30]

Homology

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A table comparing the divergence of PRR29 in different species relative to the human gene.

PRR29 has a single known paralog, C21orf58.[31] PRR29 is well conserved among chordates and PRR29-like proteins containing the DUF 4587 have been predicted in protostomes, such as Mollusca and Annelida.[32] DUF 4587 is highly conserved in all PRR29 orthologs and is also present in its paralog, C21orf58.[33] This domain has been found in species as distantly related as Capitella teleta, which diverged from humans 847 million years ago.[34]

PRR29 Expression[27]

This gene has orthologs in other animal species. It has only been found in vertebrates with the oldest being the whitespotted bamboo shark.[35][36]

PRR29 does not have any known paralogs.[35]

Genus and Species Common Name Divergence date from human (MYA)[37] Protein accession # [38] Sequence Length (aa) Identity to human sequence Similarity to human sequence
Homo sapiens Human 0 NP_001177958.1 236 1 1
Nannospalax galili Blind mole-rat 90.9 XP_008844796.1 181 0.62 0.68
Bubalus bubalis Water buffalo 97.5 XP_006041674.1 236 0.56 0.65
Monodelphis domestica opossum 163.7 XP_007482631.1| 195 0.51 0.62
Aquila chrysaetos canadensis Golden eagle 320 XP_011593496.1 170 0.36 0.48
Anolis carolinensis Anole Lizard 320.5 XP_008111611.1 186 0.39 0.52
Xenopus laevis African clawed frog 355.7 NP_001079741.1 309 0.34 0.49
Esox lucius Northern Pike 429 XP_010873077.1 197 0.48 0.74
Branchiostoma floridae lancelet 733 XP_002603029.1 1341 0.37 0.71
Ciona intestinalis Ciona intestinalis 733 XP_009857401.1 227 0.43 0.67
Capitella teleta Capitella teleta 847 ELU01749 558 0.37 0.51
Lottia gigantea Owl limpet 847 XP_009046359.1 299 0.33 0.54
PRR29 Unrooted Phylogenetic Tree[39]

Evolution

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PRR29's rate of mutation compared to that of cytochrome c and fibrinogen alpha

This gene evolves at a rate higher than that of cytochrome c but lower than that of fibrinogen alpha chain.[36]

Clinical Significance

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It is unknown if PRR29 is directly linked to any diseases.

Experiments have been performed on tissue and cell samples in order to observe any potential changes in expression of the protein under different conditions. Samples inflicted with pulmonary sarcoidosis and small cell lung cancer did not experience and significant changes in expression compared to normal cells.[40][41] Intracranial artery aneurysm did induce change, leading to heightened expression[42]

References

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  1. ^ a b c GRCh38: Ensembl release 89: ENSG00000224383 – Ensembl, May 2017
  2. ^ a b c GRCm38: Ensembl release 89: ENSMUSG00000009210 – Ensembl, May 2017
  3. ^ "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  4. ^ "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  5. ^ a b "RecName: Full=Proline-rich protein 29 - Protein - NCBI". www.ncbi.nlm.nih.gov.
  6. ^ a b c d e "PRR29 proline rich 29 [Homo sapiens (human)] - Gene - NCBI". www.ncbi.nlm.nih.gov. Retrieved 2016-04-28.
  7. ^ "PRR29_HUMAN". Uniprot. Retrieved 28 April 2016.
  8. ^ a b "PRR29 proline rich 29 [Homo sapiens (human)] - Gene - NCBI". www.ncbi.nlm.nih.gov.
  9. ^ "Human Gene PRR29 (ENST00000425164.7) from GENCODE V38". genome.ucsc.edu.
  10. ^ "NCBI Aceview".
  11. ^ "PRR29 proline rich 29 [Homo sapiens (human)] - Gene - NCBI". www.ncbi.nlm.nih.gov. Retrieved 2016-05-09.
  12. ^ "Compute pI/Mw". SIB Swiss Institute of Bioinformatics.
  13. ^ https://web.expasy.org/cgi-bin/compute_pi/pi_tool[permanent dead link]
  14. ^ "PRR29 - Proline-rich protein 29 - Homo sapiens (Human) - PRR29 gene & protein". www.uniprot.org. Retrieved 2016-05-09.
  15. ^ "PRR29 proline rich 29 [Homo sapiens (human)] - Gene - NCBI". www.ncbi.nlm.nih.gov.
  16. ^ "SDSC Biology Workbench-PELE".
  17. ^ "Motif Scan". myhits.sib.swiss.
  18. ^ "I-TASSER server for protein structure and function prediction". zhanggroup.org.
  19. ^ "AlphaFold Protein Structure Database". alphafold.ebi.ac.uk.
  20. ^ "RNA Folding Form". www.unafold.org.
  21. ^ "PSORT II Prediction". psort.hgc.jp. Retrieved 2016-05-09.
  22. ^ https://psort.hgc.jp/cgi-bin/runpsort.pl[permanent dead link]
  23. ^ "CBS Prediction Servers". www.cbs.dtu.dk. Retrieved 2016-05-09.
  24. ^ "MusiteDeep". www.musite.net.
  25. ^ Li D, Li S, Sun Y, Dong H, Li Y, Zhao B, Guo D, Weng C, Qiu HJ (February 2013). "Poly(C)-binding protein 1, a novel N(pro)-interacting protein involved in classical swine fever virus growth". Journal of Virology. 87 (4): 2072–80. doi:10.1128/JVI.02807-12. PMC 3571455. PMID 23221550.
  26. ^ "I-TASSER server for protein structure and function prediction". zhanglab.ccmb.med.umich.edu. Retrieved 2016-04-28.
  27. ^ a b "Home - GEO Profiles - NCBI". www.ncbi.nlm.nih.gov. Retrieved 2016-05-09.
  28. ^ "H.sapiens - Whole organism (Integrated) in PaxDb". pax-db.org. Retrieved 2016-05-09.
  29. ^ https://www.genomatix.de/cgi-bin/eldorado/eldorado.pl?s=8d52110cfa77f5d0982853f81a3ed821 [bare URL]
  30. ^ "PAXdb: Protein Abundance Database". pax-db.org.
  31. ^ "C21orf58 chromosome 21 open reading frame 58 [Homo sapiens (human)] - Gene - NCBI". www.ncbi.nlm.nih.gov. Retrieved 2016-04-28.
  32. ^ "BLAST: Basic Local Alignment Search Tool". blast.ncbi.nlm.nih.gov. Retrieved 2016-04-28.
  33. ^ EMBL-EBI, InterPro. "Domain of unknown function DUF4587 (IPR027904) < InterPro < EMBL-EBI". www.ebi.ac.uk. Retrieved 2016-05-09.
  34. ^ "TimeTree :: The Timescale of Life". www.timetree.org. Retrieved 2016-05-09.
  35. ^ a b "BLAST: Basic Local Alignment Search Tool". blast.ncbi.nlm.nih.gov.
  36. ^ a b "TimeTree :: The Timescale of Life". timetree.org.
  37. ^ "TimeTree :: The Timescale of Life". www.timetree.org. Retrieved 2016-05-09.
  38. ^ "National Center for Biotechnology Information". www.ncbi.nlm.nih.gov. Retrieved 2016-05-09.
  39. ^ "SDSC Biology Workbench-ClustalW".[permanent dead link]
  40. ^ "GDS3580 / 232972_at". www.ncbi.nlm.nih.gov.
  41. ^ "GDS4794 / 232972_at". www.ncbi.nlm.nih.gov.
  42. ^ "GDS3903 / 232972_at". www.ncbi.nlm.nih.gov.
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