PANO1

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PANO1
Identifiers
AliasesPANO1, PANO, proapoptotic nucleolar protein 1
External IDsGeneCards: PANO1
Orthologs
SpeciesHumanMouse
Entrez

101927423

n/a

Ensembl

ENSG00000288675

n/a

UniProt

I0J062

n/a

RefSeq (mRNA)

NM_001293167

n/a

RefSeq (protein)

NP_001280096

n/a

Location (UCSC)Chr 11: 0.8 – 0.8 Mbn/a
PubMed search[2]n/a
Wikidata
View/Edit Human

PANO1 is a protein which in humans is encoded by the PANO1 gene. PANO1 is an apoptosis inducing protein that is able to regulate the function of tumor suppressor.[3] More specifically, P14ARF is a protein in which in humans is modulated by the PANO1 gene. P14ARF is known to function as a tumor suppressor.[4] When PANO1 is highly expressed in the cells, it is able to modulate p14ARF by stabilizing it and protecting it from degradation.[4] With a confidence level of 5 out of 5, PANO1 has been theorized to be expressed in the nucleolus of the cell.[5] PANO1 is an intron-less gene.[3] Intron-less genes only make up about 3% of the human genome.[6] A functional analysis of these types of genes revealed that they often have tissue-specific expression in tissues such as the nervous system and testis.[6] This kind of expression is commonly associated with neuropathies, disease, and cancer.[6] The tissue types that PANO1 has the highest expression in, are the cerebellum regions of the brain as well as pituitary and testis tissues.[7]

Gene[edit]

PANO1 is also known as Proapoptotic Nucleolar Protein 1, PANO, and Pre-mRNA-splicing Factor CW22-like. PANO1 is located on human chromosome 11 at positions 797,511-799,190 and is positioned on the + strand.[8] Its protein contains 1 exon and 215 amino acids.[3]

Transcripts and proteins[edit]

PANO1 protein model with motifs generated through IBS tool at Cuckoo Workgroup

PANO1 has one isoform, isoform 1, located in the PONAB and PANTR species.[3] These isoforms have proteins with 215 and 216 amino acids, respectively.[3] No isoforms for the human PANO1 protein could be identified. Human PANO1 protein has a molecular weight of 22.8 kb and a theoretical, isoelectric point of 12.21.[3] From an analysis of the PANO1 protein, it was observed that the protein contains a low amount of lysine and a very low amount of asparagine when compared to other human proteins.[9] The same analysis indicated that the protein does not contain any hydrophobic or transmembrane regions.[9] PANO1 contains 2 cAMP phosphorylation sites, 6 N-myristoylation sites, 4 protein kinase C phosphorylation sites, 3 bipartite nuclear localization signals as well as arginine-rich and proline-rich regions. Using PSORTII, 3 discrimination of nuclear localization signals were identified.[10] Pat4 (RRRR) at position 200, Pat7 (RRRR) at position 201 and a bipartite (RKGTPTARCLGQRTKEK) at position 35.[10] Nuclear localization signals allow proteins to be able to enter the nucleus, but many nuclear proteins possess their own.[10] PANO1 overlaps solute carrier family 25 member 22 (SLC25A22).[5] A causal link between this solute carrier, when upregulated, has been strongly associated with an osteosarcoma's ability to proliferate.[11] In addition to promoting proliferation, SLC25A22 when expressed in vitro, progressed the cell cycle and inhibited apoptosis.[11] It is curious that PANO1, an apoptosis inducer, and SLC25A22, an apoptosis inhibiter, overlap one another.

Predicted secondary structure of PANO1 protein generated from Phyre2 and annotated to show alpha helices as well as a beta strand

Structure[edit]

The structure of PANO1 is 82% disordered meaning the protein is able to move around easily.[12] The secondary structure reveals a beta strand at positions 3-9 as well as alpha helices incorporated throughout.[12]

Gene level regulation[edit]

Promoter[edit]

One promoter region was identified using Genomatix. It is located on the positive strand and is 1040 bp in length.[13] Its start site is located at 795633 and it ends at 796672.[13] It overlaps with the primary transcript which starts at 796633.[13] 440 transcription factors were identified within the promoter region.[13] To highlight some of relevance and importance to PANO1: Wilms tumor suppressor, spermatogenic zip 1 transcription factor, signal transducer and activator of transcription, pleomorphic adenoma gene, general transcription factor IIIA, stimulating protein 1, CCAAT/enhancer binding protein, GC box elements and HMG box-containing protein 1.

Expression[edit]

Like previously mentioned, PANO1 is detected to be most expressed in the cerebellum, pituitary and testis tissues.[7] Furthermore, NCBI Geo profiles indicated that PANO1 is highly expressed in B-lymphocytes, liposarcomas, and the testis cell lines.[14] It also appears that PANO1 is highly expressed in the androgen-sensitive LAPC-4 cell line with a rank of 97.  PANO1 is biased to being expressed in androgen sensitive cells compared to androgen insensitive cells.[14]

Transcript level regulation[edit]

Predicted 3' UTR DNA folding structure generated from Unafold program and annotated to be able to see stem loops.

A predicted 3' UTR structure was generated using Unafold and depicts predicted stem loop structures.[15] Two stem loop structures are zoomed in on.

Protein level regulation[edit]

A possible cleavage site was identified between amino acids 33 and 34 as depicted in the PANO1 protein model.[3] As mentioned previously, 6 N-myristoylation sites, 2 cAMP phosphorylation sites, and 4 protein kinase C phosphorylation sites are also present.[3]

Protein motif locations
Motif Location (aa)
N-myristoylation site 23-28
N-myristoylation site 33-38
N-myristoylation site 71-76
N-myristoylation site 111-116
N-myristoylation site 120-125
N-myristoylation site 186-191
cAMP phosphorylation site 35-38
cAMP phosphorylation site 136-139
protein kinase C phosphorylation site 34-36
protein kinase C phosphorylation site 40-42
protein kinase C phosphorylation site 57-59
protein kinase C phosphorylation site 191-193

Homology and evolutionary history[edit]

Orthologs and phylogenic tree[edit]

Phylogenic tree of PANO1 generated using date of divergence data.

PANO1 orthologs were only able to be traced back in divergence to birds. Much more closely related orthologs include primates, as well as marsupial and placental mammals.[16] Specific examples of orthologs can be seen in the table below.

Genus & species Common name Tax. group Date of divergence (MYA) Accession # Seq. length (aa) Seq. identity to HSA prot. (%) Seq. identity to HSA prot. (#/100) Seq. similarity to HSA prot. (%) n m
Homo sapiens Human human 0 XP_034607700.1 215 100 1 100 0 0
Pongo abelii Sumatran orangutan primate 15.76 XP_024111240.1 216 96.3 0.963 100 0.037 3.770186718
Sapajus apella tufted capuchin primate 43.2 XP_024111240.1 216 96.3 0.963 100 0.037 3.770186718
Hylobates moloch silvery gibbon primate 19.8 XP_032005218.1 175 95.43 0.9543 81 0.0457 4.677719156
Rhinopithecus roxellana golden monkey primate 28.21 XP_030773457.1 239 86.63 0.8663 86 0.1337 14.35240101
Callithrix jacchus white-tufted-eared marmoset primate 42.9 XP_009007032.2 268 72.5 0.725 91 0.275 32.15836241
Propithecus coquereli Coquerel's sifaka primate 74.1 XP_012507388.1 183 69.28 0.6928 71 0.3072 36.70139217
Phascolarctos cinereus koala marsupial 160 XP_020836186.1 205 28.5 0.285 0.715 125.5266099
Leptonychotes weddellii Weddell seal placental 96 XP_030893169.1 182 47.88 0.4788 70 0.5212 73.64723053
Phoca vitulina harbor seal placental 96 XP_032270736.1 264 54.55 0.5455 67 0.4545 60.60524737
Loxodonta africana African bush elephant placental 105 XP_010600675.1 204 39 0.39 85 0.61 94.16085399
Orcinus orca killer whale placental 96 XP_012391505.1 237 41.21 0.4121 91 0.5879 88.64892406
Felis catus house cat placental 96 XP_023096045.1 217 59.86 0.5986 0.4014 51.31616836
Ursus arctos horribilis grizzly bear placental 96 XP_026346196.1 290 60.34 0.6034 53 0.3966 50.51749523
Oxyura jamaicensis ruddy duck bird 312 XP_035173110.1 278 29.26 0.2926 0.7074 122.894879
Melopsittacus undulatus budgerigar bird 312 XP_033919672.1 228 28.73 0.2873 0.7127 124.7228313

Divergence[edit]

Date of divergence in millions of years vs. "m" (changes / 100 amino acids) graph comparing PANO1 to two different proteins, fibrinogen alpha as well as cytochrome c.

PANO1 was compared to two other genes, fibrinogen alpha chain as well as cytochrome C. The date of divergence as well as amino acid changes were tracked over many different species types to generate a divergence date vs. number of amino acids changes as seen to the right. PANO1 appears to diverge much more quickly than fibrinogen alpha and much more quickly than cytochrome c.

Interacting proteins[edit]

p14ARF is a protein that is a known tumor suppressor.[4] It does this by controlling cell proliferation and cell survival, however the mechanism for how this process is controlled/modulated remained unclear.[4] PANO1 has been identified to modulate and stabilize p14ARF by stabilizing it and protecting it from degradation in HeLa cells.[4] When PANO1 is over-expressed, as a direct result, p14ARF expression also increases.[4]

Clinical significance[edit]

When there is an abnormal expression of PANO1 in HeLa cells, scientists have seen a decrease in tumorigenicity in nude mice.[4] Additionally, other diseases that have been associated with PANO1 include hemochromatosis 2.[5]

References[edit]

  1. ^ a b c GRCh38: Ensembl release 89: ENSG00000288675 – Ensembl, May 2017
  2. ^ "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  3. ^ a b c d e f g h "PANO1 - Proapoptotic nucleolar protein 1 - Homo sapiens (Human) - PANO1 gene & protein". www.uniprot.org. Retrieved 2021-08-01.
  4. ^ a b c d e f g Watari A, Li Y, Higashiyama S, Yutsudo M (February 2012). "A novel proapoptotic gene PANO encodes a post-translational modulator of the tumor suppressor p14ARF". Exp Cell Res. 318 (3): 187–95. doi:10.1016/j.yexcr.2011.10.019. PMID 22094112.
  5. ^ a b c "PANO1". www.genecards.org. Retrieved 2021-07-30.
  6. ^ a b c Grzybowska EA (July 2012). "Human intronless genes: functional groups, associated diseases, evolution, and mRNA processing in absence of splicing". Biochem Biophys Res Commun. 424 (1): 1–6. doi:10.1016/j.bbrc.2012.06.092. PMID 22732409.
  7. ^ a b "Human BLAT Search". genome.ucsc.edu. Retrieved 2021-08-01.
  8. ^ "GeneLoc Integrated Map for Chromosome 11: Search Results". genecards.weizmann.ac.il. Retrieved 2021-08-01.
  9. ^ a b "SAPS < Sequence Statistics < EMBL-EBI". www.ebi.ac.uk. Retrieved 2021-08-01.
  10. ^ a b c "PSORT II Prediction". psort.hgc.jp. Retrieved 2021-08-01.
  11. ^ a b Chen MW, Wu XJ (January 2018). "SLC25A22 Promotes Proliferation and Metastasis of Osteosarcoma Cells via the PTEN Signaling Pathway". Technol Cancer Res Treat. 17: 1533033818811143. doi:10.1177/1533033818811143. PMC 6259056. PMID 30482097.
  12. ^ a b "Phyre 2 Results for PANO1_phyre2". www.sbg.bio.ic.ac.uk. Retrieved 2021-08-01.
  13. ^ a b c d "Genomatix Software Suite". Genomatix.
  14. ^ a b "PANO1 - GEO Profiles - NCBI". www.ncbi.nlm.nih.gov. Retrieved 2021-08-01.
  15. ^ "DNA folding results on 21Aug01-20-42-28 for 73.242.41.233". www.unafold.org. Retrieved 2021-08-01.
  16. ^ "Protein BLAST: search protein databases using a protein query". blast.ncbi.nlm.nih.gov. Retrieved 2021-08-01.
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