C21orf58

The gene is located on the minus strand of the distal half of the long arm of Chromosome 21 at 21q22.3.[4] Transcript 1, including UTRs, is 22,740 bp and spans the chromosomal locus 46,301,130-46,323,875.[4]

mRNA transcript variants 1-5 encode two validated protein isoforms of C21orf58.[5][4] Transcript variant 1 encodes the longer, primary isoform (1) (Accession: NP_470860).[3] Transcript variants 2-5 encode the shorter isoform (2).[4] Isoform 2 has a distinct N-terminus in comparison to Isoform 1 resulting from the use of an alternative start codon.[4] A domain of unknown function, DUF4587, is conserved in all variants.[4]

The primary encoded protein consists of 322 amino acids, 8 total exons, and a molecular weight of 39.0 kDa.[3][6][7] The predicted isoelectric point is 10.06, supporting predicted nuclear localization.[7][6]

Human protein C21orf58 Isoform 1 is rich in proline and glutamine, and poor in cysteine, phenylalanine, and tyrosine.[7] The protein is particularly tyrosine poor containing zero tyrosine residues.[7] Isoform 1 contains 20 more positive charged residues than negative charged residues providing additional support for the predicted isoelectric point.[7]

Illustration of C21orf58 annotated with important domains, motifs, and post-translational modifications.

C21orf58 Isoform 1 has three conserved domains: proline-rich domain, histidine rich domain, and DUF4587. Proline-rich domain, Pro¹⁷⁵-Pro³²², is predicted to mediate protein-protein interactions.[8] Histidine-rich repeat domain, His²⁹²-His²⁹⁹, is predicted to facilitate localization.[9][10] The domain of unknown function, DUF4587 (Arg²³⁴- His²⁹¹⁾, is a member of pfam15248 exclusively found in eukaryotes.[11]

C21orf58 contains a nuclear localization signal, The¹³⁵-Leu¹⁴⁴.[12]

Tertiary structure of C21orf58 predicted by Phyre2[13]

Secondary structure of C21orf58 is predicted to consist primarily of random coil domains with four regions of alpha helices throughout the span of the protein.[14][15][16] Secondary structure predictions of C21orf58 orthologs revealed similar results; random coil and four regions of alpha helices with the addition of beta-sheets throughout.[14][15][16]

C21orf58 mRNA transcript variant 1 aligned and conceptually translated with important domains, motifs, and post-translational modifications.

C21orf58 is predicted to undergo multiple post-translational modifications including phosphorylation, O-GlcNAc, and SUMOylation.[17][18][19][20]

Immunocytochemistry revealed localization of C21orf58 to nucleoplasm and nuclear bodies.[21] Presence of a nuclear localization sequence provides further evidence for protein import into the cell nucleus.[14]

Subcellular localization predictions for C21orf58 based on the amino acid sequence (PSORTII) suggested nuclear localization.[22] Predictions across orthologs agreed with nuclear localization.[22]

C21orf58 is constitutively expressed at low levels across various normal tissues (GDS3113), including but not limited to brain, endocrine, bone marrow, lung, and reproductive tissues.[23]

C21orf58 constitutive low level expression across all tissues analyzed (GDS3113)[24]

DNA microarray analysis from various experiments showed variable C21orf58 expression in unique physiological conditions.

• An elevated level of C21orf58 expression was observed in astrocytes treated with harmane, a chemical compound associated with essential tremor (ET), compared to control (GDS2919).[25]
• C21orf58 expression up-regulated and then down-regulated in T lymphocytes over time following exposure to Azaspiracid-1 (AZ-10), a marine phycotoxin (GDS3429).[26]
• C21orf58 expression was found to be up-regulated in teratozoospermic individuals compared to expression in normospermic individuals (GDS2697).[27] Teratozoospermia is a condition where sperm have abnormal morphology affecting male fertility.[28]

C21orf58 was found to be expressed through all stages of development at similar levels throughout.[29]

Sagittal plane view of the mouse brain in situ hybridization of C21orf58 otholog in mouse (2610028H24ik). Expression of C21orf58 color-coded by expression intensity ranging from blue (low intensity) through green to red (high intensity).[26] Allen Brain Atlas

C21orf58 ortholog in mouse 2610028H24Rik was found to be ubiquitously expressed at high levels throughout the mouse brain.[30]

The primary promoter for the longest variant of C21orf58 aligns with the start of the 5'UTR and is 1143bp in length.[31] The predicted promoter sequence overlaps with the 5'UTR and coding sequence of Pericentrin (PCNT) on the plus strand of Chromosome 21. Predicted transcription factors are associated with regulation of the cell cycle, neurogenesis, early development, and sex determination.

No human paralogs for C21orf58 were identified.[49]

C21orf58 orthologs were identified in bony fish but not in cartilaginous fish.[50] The first 35 bases of DUF4587, Arg²³⁴- Pro²⁶⁵, were conserved across ortholog sequences.[51] The most distantly related ortholog identified was the zebrafish.[50]

The rate of C21orf58 evolution was determined through an application of the Molecular Clock Hypothesis. Through comparison with alpha fibrinogen and cytochrome C, it was determined that C21orf58 has evolved at an intermediate rate.

m vs Divergence from Humans (MYA). C21orf58 compared to a quickly evolving gene (α fibrinogen) and a slowly evolving gene (Cytochrome C) across orthologs.