NOXRED1 explained

NADP-dependent oxidoreductase domain-containing protein 1 is a protein that in humans is encoded by the NOXRED1 gene. An alias of this gene is Chromosome 14 Open Reading Frame 148 (c14orf148). This gene is located on chromosome 14, at 14q24.3.[1] [2] NOXRED1 is predicted to be involved in pyrroline-5-carboxylate reductase activity as part of the L-proline biosynthetic pathway. It is expressed in a wide variety of tissues at a relatively low level, including the testes, thyroid, skin, small intestine, brain, kidney, colon, and more.

Gene

NOXRED1 is coded on the minus strand of the human Chromosome 14 from nucleotides 77,394,021-77,423,523. It has a total of 9 exons and 8 introns, and it spans a total of 29,502 bases.

Neighborhood

The gene neighborhood of NOXRED1 includes Transmembrane p24 TraffickingProtein Family Member 8 (TMED8), Sterile Alpha Motif Domain 15 (SAMD15), VPS33B Interacting Protein (VIPAS39), and Activator of HSP90 ATPase Activity 1 (AHSA1).

Transcripts

NOXRED1 has three known mRNA isoforms (table 2).[3] The primary isoform is 2324 bases in length and is composed of 6 exons.[4] Isoform 2[5] and Isoform 3[6] are 1773 and 1770 nucleotides long, respectively.

Proteins

NADP-dependent oxidoreductase domain-containing protein 1 (NOXRED1) is a protein which in humans is encoded by the gene NOXRED1.[7] It is 359 residues long and has a molecular weight of ~39.9 kDa. This protein is enriched in leucine residues, in comparison to other human proteins.[8] NOXRED1 is predicted to localize in the cytoplasm and perform functions involving pyrroline-5-carboxylate reductase. From residues 78-189, NOXRED1 contains the conserved protein domain family pyrroline-5-carboxylate reductase (ProC).

Protein isoforms

NOXRED1 has three known protein isoforms (Table 2).[9] [10] Isoform 1 is the largest and most abundant.

IsoformAccession NumbermRNA Length (nucleotides)Accession NumberProtein Length (amino acids)Molecular Weight (kDa)
1NM_001113475.32324NP_001106946.135939.9
2NM_001394980.11773XP_011534731.126929.8
3XM_011536429.41770XP_016876458.123425.9
Isoforms of NOXRED1. Information obtained from NCBI Nucleotide[11] and NCBI Protein[12] databases.

Protein level expression

Primary Antibody Data

ThermoFisher Scientific has developed a human polyclonal antibody targeting NOXRED1. It can be used for a variety of different functions, including immunocytochemistry, immunohistochemistry, immunoprecipitation, and western blotting.[13] Additionally, the Human Protein Atlas database shows immunocytochemistry produced images of NOXRED1 within the A549, MCF-7, and U2OS cell lines[14]

In situ hybridization data

The Allen Brain Institute shows that NOXRED1 is expressed at a moderate level throughout the Mus musculus brain[15]

Protein interactions

Some predicted proteins that interact with the human NOXRED1 are Delta-1-pyrroline-5-carboxylate synthase and ornithine aminotransferase.[16] Delta-1-pyrroline-5-carboxylate synthase catalyzes the conversion of glutamate to delta-1-pyrroline-5-carboxylate synthase.[17] Ornithine aminotransferase is an enzyme that converts arginine and ornithine into glutamate and GABA.[18] Both of these proteins are involved in the proline biosynthesis pathway.

Homology and evolution

Paralogs

NOXRED1 has three orthologs. Pyrroline-5-carboxylate reductase 1 (PYCR1), pyrroline-5-carboxylate reductase 2 (PYCR2), and pyrroline-5-carboxylate reductase 3 (PYCR3) all are also involved in the synthesis of proline from pyrroline-5-carboxylate.[19] [20] [21] PYCR1 is located at 17q25.3, PYCR2 is located at 1q42.12, and PYCR3 is located at 8q24.3.

GeneGenus and SpeciesProtein Accession NumberSequence Length (aa)% Sequence Identity to Human Protein% Sequence Similarity to Human Protein
NOXRED1Homo sapiensNP_001106946.1359100100
PYCR2Homo sapiensNP_037460.232015.423.3
PYCR3Homo sapiensNP_075566.327413.623.8
PYCR1Homo sapiensNP_008838.231913.220.6
Paralogs of NOXRED1. Percent sequence identity and similarity were calculated using EMBOSS Needle.

Orthologs

NOXRED1 was found to be highly conserved throughout history—there are existing orthologs within mammals, aves, reptiles, amphibians, bony fish, cartilaginous fish, trichoplaxes, and some invertebrates.[22] [23] Interestingly, orthologs were not able to be found in one of the three orders of amphibians—Urodela. Additionally, orthologs were not able to be found in insects, fungi, protists, plants, bacteria, or archaea25. Listed in a table are a list of 20 different NOXRED1 protein orthologs from a diverse array of species, including mammals, aves, reptiles, amphibians, different classes of fish, and invertebrates.

Genus and SpeciesCommon NameTaxonomic ClassTaxonomic OrderDOD (MYA)Accession NumberAA Sequence Length% Sequence Identity to Human Protein% Sequence Similarity to Human Protein
Homo sapiensHumanMammaliaPrimata0NP_001106946.1359100100
Mus musculusMouseMammaliaRodentia87NP_082020.1 36660.676.9
Felis catusCatMammaliaCarnivora94XP_019688936.1 3817279.3
Elephas maximus indicusIndian ElephantMammaliaProboscidea99XP_049755695.138469.477.2
Struthio camelus australisSouthern OstrichAvesStruthioniformes319XP_009673940.13454460.4
Oxyura jamaicensisRuddy DuckAvesAnseriformes319XP_035184255.139243.856.8
Pygoscelis adeliaeAdélie penguinAvesSpheniscoformes319XP_009317781.132334.448.8
Mauremys muticaYellow Pond TurtleReptiliaTestudines319XP_044872068.137247.565.3
Protobothrops mucrosquamatusBrown Spotted Pit ViperReptiliaSerpentes319XP_029139298.138839.858.8
Gekko japonicusJapanese GeckoReptiliaSquamata319XP_015273827.140337.656.6
Geotrypetes seraphiniGaboon CaecilianAmphibiaGymnophiona353XP_033807528.137145.259.7
Xenopus tropicalusWestern Clawed FrogAmphibiaAnura353NP_001072734.134440.956.5
Rana temporariaCommon FrogAmphibiaAnura353XP_040189126.136736.252.4
Polypterus senegalusGray bichirActinopterygiiPolypteriformes431XP_039598035.136439.857.3
Danio rerioZebrafishActinopterygiiCypriniformes431XP_005169929.133336.853.8
Rhincodon typusWhale SharkChondrichthyesOrectolobiformes464XP_020369405.136533.350.6
Petromyzon marinusSea LamprayHyperoartiaPetromyzontiformes599XP_032812106.135925.737
Strongylocentrotus purpuratusPacific Purple Sea UrchinEchinoideaEchinoida619XP_011675891.238028.347.3
Trichoplax sp. H2Trichoplax H2Trichoplax-661RDD44387.138228.246.1
Crassostrea gigasSea OysterBivalviaOstreida694XP_011447367.236631.649.7
Table 1. Orthologs of NOXRED1. Orthologs are grouped by taxonomic class and then sorted first by increasing date of divergence (MYA) and second by percent sequence identity to the human protein. Date of divergence was calculated using the pairwise divergence median time from Timetree.org.[24] Percent sequence identity and similarity were calculated using EMBOSS Needle.[25]

Function/Biochemistry

The human NOXRED1 protein is predicted to play a role in the L-proline biosynthesis pathway.

Clinical significance

NOXRED1 has a few clinically significant associations. Chen et al., 2020 found that the variant rs8012548 (an intron variant) within NOXRED1 is significantly associated withcutaneous melanoma specific survival, meaning that patients with cutaneous melanoma who have carry rs8012548 are less likely to perish due to the disease.[26] Tabe-Bordbar et al., 2020 found that rs12890411 within intron 5 of NOXRED1 lies within an Estrogen Receptor Alpha (Erα) enhancer region.[27] This variant is an eQTL for breast cancer, and it at least partially decreases the binding affinity of the transcription factor RELA. Yuan et al., 2021 predicted that NOXRED1 influences the pathogenesis of Alzheimer's disease and mild cognitive impairment by increasing oxidative stress within the limbic region.[28] Nacita et al., 2015 reported that a patient with the interstitial deletion of 14q24-14q32 exhibits developmental and neurological delays, face dysmorphology, and epilepsy.[29] Relating to the transcript, MacNair et al., 2016 found that NOXRED1 is downregulated in the motor neurons in mice with a TDP-43 mutation related to amyotrophic lateral sclerosis (ALS).[30] Relating to the protein, Vandenbrouck et al., 2016 found that NOXRED1 is found within the proteome of human spermatozoa.[31]

Notes and References

  1. Web site: NOXRED1 NADP dependent oxidoreductase domain containing 1 [Homo sapiens (human)] - Gene - NCBI ]. 2022-09-18 . www.ncbi.nlm.nih.gov.
  2. Web site: Human hg38 chr14:77,394,021-77,423,523 UCSC Genome Browser v437 . 2022-09-28 . genome.ucsc.edu.
  3. Web site: AceView: Gene:C14orf148, a comprehensive annotation of human, mouse and worm genes with mRNAs or ESTsAceView. . 2022-09-28 . www.ncbi.nlm.nih.gov.
  4. Web site: 2022-06-10 . Homo sapiens NADP dependent oxidoreductase domain containing 1 (NOXRED1), transcript variant 1, mRNA . en-US.
  5. Web site: 2022-08-20 . Homo sapiens NADP dependent oxidoreductase domain containing 1 (NOXRED1), transcript variant 2, mRNA . en-US.
  6. Web site: 2022-04-05 . PREDICTED: Homo sapiens NADP dependent oxidoreductase domain containing 1 (NOXRED1), transcript variant X3, mRNA . en-US.
  7. Web site: NADP-dependent oxidoreductase domain-containing protein 1 isoform X1 [- Protein - NCBI |url=https://www.ncbi.nlm.nih.gov/protein/XP_011534730.1 |access-date=2022-09-18 |website=www.ncbi.nlm.nih.gov].
  8. Web site: SAPS < Sequence Statistics < EMBL-EBI . 2022-12-12 . www.ebi.ac.uk.
  9. Web site: NADP-dependent oxidoreductase domain-containing protein 1 isoform X2 [- Protein - NCBI |url=https://www.ncbi.nlm.nih.gov/protein/XP_011534731.1 |access-date=2022-12-08 |website=www.ncbi.nlm.nih.gov].
  10. Web site: NADP-dependent oxidoreductase domain-containing protein 1 isoform X3 [- Protein - NCBI |url=https://www.ncbi.nlm.nih.gov/protein/XP_016876458.1 |access-date=2022-12-08 |website=www.ncbi.nlm.nih.gov].
  11. Web site: Home - Nucleotide - NCBI . 2022-12-08 . www.ncbi.nlm.nih.gov.
  12. Web site: Home - Protein - NCBI . 2022-12-08 . www.ncbi.nlm.nih.gov.
  13. Web site: Anti-NOXRED1 Antibodies Invitrogen . 2022-12-08 . www.thermofisher.com.
  14. Web site: Subcellular - NOXRED1 - The Human Protein Atlas . 2022-12-08 . www.proteinatlas.org.
  15. Web site: ISH Data :: Allen Brain Atlas: Mouse Brain . 2022-12-08 . mouse.brain-map.org.
  16. Web site: Pharos: Target List . 2022-12-11 . pharos.nih.gov . en.
  17. Web site: ALDH18A1 aldehyde dehydrogenase 18 family member A1 [Homo sapiens (human)] - Gene - NCBI ]. 2022-12-11 . www.ncbi.nlm.nih.gov . en.
  18. Web site: OAT ornithine aminotransferase [Homo sapiens (human)] - Gene - NCBI ]. 2022-12-11 . www.ncbi.nlm.nih.gov . en.
  19. Web site: PYCR1 pyrroline-5-carboxylate reductase 1 [Homo sapiens (human)] - Gene - NCBI ]. 2022-10-22 . www.ncbi.nlm.nih.gov.
  20. Web site: PYCR2 pyrroline-5-carboxylate reductase 2 [Homo sapiens (human)] - Gene - NCBI ]. 2022-10-22 . www.ncbi.nlm.nih.gov.
  21. Web site: PYCR3 pyrroline-5-carboxylate reductase 3 [Homo sapiens (human)] - Gene - NCBI ]. 2022-10-22 . www.ncbi.nlm.nih.gov.
  22. Web site: BLAST: Basic Local Alignment Search Tool . 2022-10-22 . blast.ncbi.nlm.nih.gov.
  23. Web site: NOXRED1 Gene - GeneCards NXRD1 Protein NXRD1 Antibody . 2022-10-22 . www.genecards.org.
  24. Web site: TimeTree :: The Timescale of Life . 2022-10-22 . timetree.org . en.
  25. Web site: EMBOSS Needle < Pairwise Sequence Alignment < EMBL-EBI . 2022-10-22 . www.ebi.ac.uk.
  26. Chen K, Liu H, Liu Z, Bloomer W, Amos CI, Lee JE, Li X, Nan H, Wei Q . 6 . Genetic variants in glutamine metabolic pathway genes predict cutaneous melanoma-specific survival . Molecular Carcinogenesis . 58 . 11 . 2091–2103 . November 2019 . 31435991 . 7504905 . 10.1002/mc.23100 .
  27. abe-Bordbar S, Song YJ, Lunt BJ, Prasanth KV, Sinha S . 2020-11-09 . Mechanistic analysis of enhancer sequences in the Estrogen Receptor transcriptional program . en . 2020.11.08.373555 . 10.1101/2020.11.08.373555. 226959729 . bioRxiv .
  28. Yuan SX, Li HT, Gu Y, Sun X . Brain-Specific Gene Expression and Quantitative Traits Association Analysis for Mild Cognitive Impairment . Biomedicines . 9 . 6 . 658 . June 2021 . 34201204 . 8229744 . 10.3390/biomedicines9060658 . free .
  29. Nicita F, Di Giacomo M, Palumbo O, Ferri E, Maiorani D, Vigevano F, Carella M, Capuano A . 6 . Neurological features of 14q24-q32 interstitial deletion: report of a new case . Molecular Cytogenetics . 8 . 1 . 93 . 2015-11-24 . 26604985 . 4657200 . 10.1186/s13039-015-0196-6 . free .
  30. MacNair L, Xiao S, Miletic D, Ghani M, Julien JP, Keith J, Zinman L, Rogaeva E, Robertson J . 6 . MTHFSD and DDX58 are novel RNA-binding proteins abnormally regulated in amyotrophic lateral sclerosis . Brain . 139 . Pt 1 . 86–100 . January 2016 . 26525917 . 10.1093/brain/awv308 . free .
  31. Vandenbrouck Y, Lane L, Carapito C, Duek P, Rondel K, Bruley C, Macron C, Gonzalez de Peredo A, Couté Y, Chaoui K, Com E, Gateau A, Hesse AM, Marcellin M, Méar L, Mouton-Barbosa E, Robin T, Burlet-Schiltz O, Cianferani S, Ferro M, Fréour T, Lindskog C, Garin J, Pineau C . 6 . Looking for Missing Proteins in the Proteome of Human Spermatozoa: An Update . Journal of Proteome Research . 15 . 11 . 3998–4019 . November 2016 . 27444420 . 10.1021/acs.jproteome.6b00400 .