QSER1

Glutamine Serine Rich Protein 1 or QSER1 is a protein encoded by the QSER1 gene.[5]

QSER1
Identifiers
AliasesQSER1, glutamine and serine rich 1
External IDsMGI: 2138986 HomoloGene: 11710 GeneCards: QSER1
Gene location (Human)
Chr.Chromosome 11 (human)[1]
Band11p13Start32,892,820 bp[1]
End32,993,316 bp[1]
Orthologs
SpeciesHumanMouse
Entrez

79832

99003

Ensembl

ENSG00000060749

ENSMUSG00000074994

UniProt

Q2KHR3

n/a

RefSeq (mRNA)

NM_001076786
NM_024774

NM_001123327

RefSeq (protein)

NP_001070254

n/a

Location (UCSC)Chr 11: 32.89 – 32.99 MbChr 2: 104.75 – 104.82 Mb
PubMed search[3][4]
Wikidata
View/Edit HumanView/Edit Mouse

The function of this protein is currently unknown. QSER1 has one alias, FLJ21924.[5]

Gene

Location

The QSER1 gene is found on the short arm of chromosome 11 (11p13), beginning at 32,914,792 bp and ending at 33,001,816 bp. It is 87,024 bp in length. It is located between the genes DEPDC7 and PRRG4 and is 500,000 bp downstream from the Wilms Tumor 1 gene (WT1), which is implicated in multiple pathologies.[5][6]

Homology

Orthologs

QSER1 is highly conserved in most species of the clade Chordata. Orthologs have been found in primates, birds, reptiles, amphibians, and fish as far back as the coelacanth, which diverged 414.9 million years ago.[5][6]

Paralogs

QSER1 has one paralog in humans, Proline-rich 12, or PRR12. PRR12 is found on chromosome 9 at 9q13.33, which does not have known function. PRR12 is found in most chordate species as far back as the coelacanth.[7] The duplication event likely occurred sometime in the chordate lineage near the divergence of the coelacanth. Both PRR12 and QSER1 contain the conserved DUF4211 domain near the 3’ ends of the genes.[5][7]

mRNA

Promoter and transcription factors

The promoter region for QSER1 is 683 bp in length and is found on chromosome 11 between 32,914,224 bp and 32,914,906. There is some overlap between the promoter region and the 5’ UTR of QSER1. Predicted transcription factors with conservation include (but are not limited to) EGR1, p53, E2F3, E2F4, PLAG1, NeuroD2, Myf5, IKAROS1, SMAD3, KRAB, MZF1, and c-Myb.[8]

Expression

Normal expression

Expression of QSER1 is seen at levels lower than 50% in many tissues. However, notable expression is seen in skeletal muscle, the appendix, trigeminal ganglia, cerebellum peduncles, pons, spinal cord, ciliary ganglion, globus pallidus, subthalamic nucleus, dorsal root ganglion, fetal liver, adrenal gland, ovary, uterus corpus, cardiac myocytes, the atrioventricular node, skin, pituitary gland, tongue, early erythroid progenitors, and tonsil.[9][10]

NCBI GeoProfiles expression data for QSER1

Differential expression

A notable decrease in QSER1 expression has been noted in renal mesangial cells in response to treatment with 25 mM glucose. This condition was studied as differential expression of genes involved in cell cycle regulation had been noted in these cells in response to high glucose levels seen with diabetes mellitus.[11][12] A different study noted overexpression of QSER1 in pathological cardiomyopathy. This condition is associated with altered expression of genes involved in immune responses, signaling, cell growth, and proliferation as well as infiltration of B lymphocytes.[13][14]

Differential expression of QSER1 is seen in multiple cancer conditions. Overexpression of QSER1 was noted in Burkitt’s Lymphoma.[9] QSER1 expression also increases with increasing Gleason score (more advanced stages) of prostate cancer.[15] In a study on breast cancer response to paclitaxel and fluorouracil‐doxorubicin‐cyclophosphamide chemotherapy, it was noted that breast cancer lines with higher levels of QSER1 were more likely to respond to treatment than those with underexpression of QSER1.[16] Greater expression of QSER1 was also noted in mammary epithelial cells of immortalized cell lines than in mammary epithelial cells from cell lines with finite lifespan.[17]

3’ UTR

Over 20 stem loops are predicted in the 3’ UTR of QSER1. 16 stem loops are found within the first 800 bp of 3’ UTR.[18] The 3’ UTR is almost entirely conserved in mammals with less conservation seen in other organisms.[19]

Protein

General properties
QSER1 protein overview

QSER1 protein is 1735 amino acids in length.[20] The composition of the peptide is significantly high in serine and glutamine: 14.7% serine residues and 8.9% glutamine.[21]

Conservation

QSER1 protein is highly conserved in chordate species. The table below shows information on the protein orthologs.

Tree of QSER1 Orthologs
Genus and species nameCommon nameProtein accession number[22]Sequence Identity to human protein[22]
Homo sapiensHumansNP_001070254.1
Pan troglodytesChimpanzeeXP_508354.399%
Macaca mulattaRhesus macaqueNP_001244647.198%
Callithris jacchusMarmosetXP_002755192.196%
Ailuropoda melanoleucaGiant pandaXP_002917539.190%
Loxodonta africanaElephantXP_003412344.188%
Mus musculusMouseNP_001116799.181%
Monodelphis domesticaOpossumXP_001368629.171%
Ornithorhynchus anatinusPlatypusXP_001506659.275%
Taeniopygia guttataZebra finchXP_002195876.169%
Gallus gallusChickenNP_001186343.169%
Anolis carolinensisCarolina anole (lizard)XP_003214747.162%
Takifugu rubripesJapanese pufferfishXP_003977915.148%
Latimeria chalumnae CoelacanthN/A62%

Domains and motifs
PSORT prediction of conserved nuclear localization and nuclear localization signals in QSER1 protein

QSER1 protein contains two high conserved domains found not only in QSER1 but also in other protein products. These include the PHA02939 domain from amino acid 1380-1440 and the DUF4211 domain from amino acid 1522-1642.[23][24] Nuclear localization was predicted by pSORT. This property was conserved from the human QSER1 to the coelacanth QSER1. Multiple conserved nuclear localization signals were also predicted within the QSER1 protein by pSORT.[25]

Structure

Predictions of the QSER1 protein structure indicate that the protein contains many alpha helices.[26][27][28] NCBI cBLAST predicted structural similarity between the QSER1 protein and the Schizosaccharomyces pombe (fission yeast) RNA Polymerase II A chain. The two regions of similarity occur between amino acids 56-194 and 322-546.[27] This first region (56-194) is a regulatory region in both the human and yeast RNA Polymerase II containing multiple repeats of the sequence YSPTSPSYS. Phosphorylation of serine residues in this region regulates progression through the steps of gene transcription.[29] A 3D structure was provided for this region. The structurally similar region is on the exterior of the protein molecule and forms part of the DNA binding cleft.

Further structural similarity to a viral RNA Polymerase binding protein was predicted by Phyre2.[28] This structure is found at the very end of the protein between amino acids 1671-1735. The structure has a long region of alpha helices that were also predicted by SDSC Biology Workbench PELE. An image of the structurally similar region and sequence alignment is shown on the right. Regions before the identified structurally similar domain show two other alpha helices predicted with high confidence.[28]

Post translational modifications

Phosphorylation
ExPASy NetPhos Predicted Phosphorylation Sites

There are 12 confirmed phosphorylation sites on the QSER1 protein. Eight are phosphoserines, one phosphotyrosine, and three phosphothreonines. Three of these sites have been shown to be phosphorylated by ATM and ATR in response in DNA damage.[30] 123 other possible phosphorylation sites have been predicted using the ExPASy NetPhos tool.[31]

SUMOylation

Interaction of QSER1 protein with SUMO has been noted in multiple proteome-wide studies.[32][33] Predicted SUMOylation sites have been found in QSER1 protein. Highly conserved SUMOylation sites occur with the sequence MKMD at amino acid 794, VKIE at 1057, VKTG at 1145, LKSG at 1157, VKQP at 1487, and VKAE at 1492 .[34]

Predicted SUMOylation Sites in QSER1 protein

Interactions

ATM/ATR

Phosphorylation of QSER1 at three serine residues, S1228, S1231, and S1239, by ATM and ATR in response to DNA damage was found in a proteome-wide study.[30]

SUMO

Interaction of QSER1 with SUMO has been confirmed in multiple studies.[32][33] The role of SUMOylation in QSER1 function is unclear. However, there may be a connection between QSER1 and SUMO in response to endoplasmic reticulum stress (often caused by accumulation of misfolded proteins). In a study on ER stress, QSER1 was tagged as an ER stress response gene with altered expression.[35] Further, in a study on SUMOylation in response to accumulated misfolded proteins and ER stress found QSER1 to be a SUMO interactant in this situation.[32] Any connection between these two activities is unstudied and unconfirmed.

RNA polymerase II

Direct interaction of QSER1 with RNA polymerase II was found in a study performed by Moller, et al. Interaction was shown to occur with the DNA-directed RNA polymerase II subunit, RPB1, of RNA polymerase II during both mitosis and interphase. Colocalization/interaction of QSER1 was shown to the regulatory region of RPB1 with 52 heptapeptide (YSPTSPSYS) repeats.[29]

NANOG and TET1

Interaction between homeobox protein NANOG and Tet methylcytosine dioxygenase 1 (TET1) has been shown to be important in establishing pluripotency during the generation of induced pluripotent stem cells. QSER1 protein was shown to interact with both NANOG and TET1.[36]

Ubiquitin

QSER1 was found to interact with ubiquitin in two proteome-wide substrate studies.[37][38] Specific details about this interaction have not been studied.

Pathology

Altered expression of QSER1 is noted in pathological cardiomyopathy, Burkitt's Lymphoma, prostate cancer, and some breast cancers mentioned above.[8][9][13][15] NCBI AceView lists multiple mutations associated with other pathologies including an eight base pair and 13 base pair deletion in QSER1 associated with leiomyosarcoma of the uterus, and 57 base pair difference in a neuroblastoma. Also listed are multiple splice variants with truncated 5' and/or 3' ends often noted in cancerous conditions.[39] Further, according to the NCBI OMIM database, multiple pathologies are associated with alterations in the 11p13 region and therefore may implicate QSER1.[40] These include Exudative Vitreoretinopathy 3,[41] Familial Candidiasis 3,[42] Centralopathic Epilepsy,[43] and Autosomal Recessive Deafness 51.[44] QSER1 was also noted as a susceptibility gene for Parkinson's disease.[35]

gollark: I really only want tasks, cancel and py.
gollark: no u.
gollark: I don't want to pull in this entire jishaku thing, but I could probably steal just its command queue or even just make it unsafely run synchronously.
gollark: ++protocol_epsilon 398dddeac6333b99915b3a4f22c1a70c152e0aeef62bbe4fe2038696f2e7eb0b
gollark: OR CAN IT?

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