CLIP4
Identifiers
Aliases	CLIP4, RSNL2, CAP-Gly domain containing linker protein family member 4
External IDs	MGI: 1919100; GeneCards: CLIP4
Available structures PDB Ortholog search: PDBe RCSB List of PDB id codes 2Z0W
Gene location (Human) Chr. Chromosome 2 (human)[2] Band 2p23.2 Start 29,097,705 bp[2] End 29,199,777 bp[2]
Gene location (Mouse) Chr. Chromosome 17 (mouse)[3] Band 17|17 E1.3 Start 72,075,468 bp[3] End 72,171,268 bp[3]
RNA expression pattern Bgee Human Mouse (ortholog) Top expressed in secondary oocyte skin of thigh Skeletal muscle tissue of biceps brachii Skeletal muscle tissue of rectus abdominis germinal epithelium skin of hip gastrocnemius muscle sural nerve skin of abdomen external globus pallidus Top expressed in seminiferous tubule cardiac muscle tissue of left ventricle spermatid digastric muscle soleus muscle sternocleidomastoid muscle extensor digitorum longus muscle skin of external ear masseter muscle temporal muscle More reference expression data BioGPS n/a
Orthologs Databases NCBI: entry; OMA: entry Species Human Mouse Entrez 79745 78785 Ensembl ENSG00000115295 ENSMUSG00000024059 UniProt Q8N3C7 Q8CI96 RefSeq (mRNA) NM_001287527 NM_001287528 NM_024692 NM_001271483 NM_001271484 NM_030179 NM_175378 RefSeq (protein) NP_001274456 NP_001274457 NP_078968 NP_001258412 NP_001258413 NP_084455 NP_780587 Location (UCSC) Chr 2: 29.1 – 29.2 Mb Chr 17: 72.08 – 72.17 Mb PubMed search [4] [5]
Wikidata
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CAP-Gly Domain Containing Linker Protein Family Member 4 is a protein that in humans is encoded by the CLIP4 gene.^[6] In terms of conserved domains, the CLIP4 gene contains primarily ankyrin repeats and the eponymous CAP-Gly domains.^[6] The structure of the CLIP4 protein is largely made up of coil, with alpha helices dominating the rest of the protein.^[7] CLIP4 mRNA expression occurs largely in the adrenal cortex and atrioventricular node.^[8] The literature encompassing CLIP4's conserved domains and paralogs points toward microtubule regulation as a possible function of CLIP4.

The human CLIP4 gene, also known as Restin-Like Protein 2 (RSNL2),^[9] is located on the plus strand of the short (p) arm of chromosome 2 at region 2, band 3^[9] from base pair 29,096,676 to base pair 29,189,643. CLIP4 is 92,968 base pairs in length and consists of 23 exons.^[9]

The human CLIP4 protein is 705 amino acids in length and is composed of two main types of conserved domains: Two CAP-Gly domains and numerous ankyrin repeats.^[9] The secondary structure of CLIP4 consists largely of random coil, with alpha helices as the second-most abundant structure and beta sheets as the third-most abundant structure.^[7]

The isoelectronic point of the unprocessed CLIP4 protein is slightly basic (8.62 pI), meaning there is a slight excess of basic amino acids compared to acidic amino acids.^[13] The molecular weight is about 65 kD.^[13] The most abundant amino acid in CLIP4 is Serine, which makes up 10.7% of the protein.^[14] Aligned matching blocks of separated, tandem, and periodic repeats are found between positions 340-345 and 542-547, as well as 447-547 and 564-568.^[14] The unusual 9-figure periodic element of a singular Lysine followed by eight other amino acids occurs five times within the protein when compared to the swp23s.q dataset.^[14] Another unusual phenomenon is a 7-figure periodic element of a negatively charged amino acid followed by six other hydrophobic amino acids, which occurs six times within the protein when compared to the swp23s.q dataset.^[14] There are two instances of Serine spacing and two instances of Phenylalanine spacing that comprise unusually large distances when compared to the swp23s.q dataset.^[14]

CLIP4 RNA expression is consistently measured to a high degree in the thyroid.^[6] Additionally, high degrees of transcription occur in the adrenal cortex and atrioventricular node.^[8] The Human Protein Atlas points toward high RNA expression values in the muscle tissues, as well as some in the skin, endocrine tissues, and proximal digestive tract.^[17] Greatest protein expression values appeared in the muscle tissues as well, in addition to some in the lung, gastrointestinal tract, liver & gallbladder, and bone marrow & lymphoid tissues.^[17]

CLIP4 protein expression seems to be highly expressed during Ada3 deficiency.^[18] There also exists a higher trend towards higher CLIP4 expression in the absence of U28.^[18]

These transcription factors were chosen and organized based on proximity to the promoter and matrix similarity.^[19]

The human CLIP4 mRNA sequence has 12 stem-loop structures in its 5' UTR and 13 stem-loop structures in its 3' UTR. Of those secondary structures, there are 12 conserved stem-loop secondary structures in the 5'UTR as well as 1 conserved stem-loop secondary structure in the 3' UTR.^[20]

The human CLIP4 protein is localized within the cellular nuclear membrane.^[21] CLIP4 does not have a signal peptide due to its intracellular localization.^[22] It also does not have N-linked glycosylation sites for that same reason.^[23] CLIP4 is not cleaved.^[24] However, numerous O-linked glycosylation sites are present.^[25] A high density of phosphorylation sites are present in the 400-599 amino acid positions on the CLIP4 protein, although many are also present throughout the rest of the protein.^[26]

CAP-Gly domains are often associated with microtubule regulation.^[27] In addition, ankyrin repeats are known to mediate protein-protein interactions.^[28] Furthermore, CLIP1, a paralog of CLIP4 in humans, is known to bind to microtubules and regulate the microtubule cytoskeleton.^[29] The CLIP4 protein is also predicted to interact with various microtubule-associated proteins.^[30] As a result, it is likely that the CLIP4 protein, although uncharacterized, is associated with microtubule regulation.

The CLIP4 protein is predicted to interact with many proteins associated with microtubules; namely, MAPRE1, MAPRE2, and MAPRE3. It is also predicted to interact with CKAP5 and DCTN1, a cytoskeleton-associated protein and dynactin-associated protein respectively.^[30]

CLIP4 activity is correlated with the spread of renal cell carcinomas (RCCs) within the host and could therefore be a potential biomarker for RCC metastasis in cancer patients.^[31] Additionally, measurement of promotor methylation levels of CLIP4 using a Global Methylation DNA Index reveals that higher methylation of CLIP4 is associated with an increase in severity of gastritis to possibly gastric cancer.^[32] This indicates that CLIP4 could be used for early detection of gastric cancer.^[33] A similar finding was also documented for prostate cancer, in which CLIP4 was found to be hypermethylated in patients with prostate cancer.^[34]

The presence of CLIP4 was found to be highly increased in samples with predicted severe fibrosis as a result of Chronic Hepatitis C virus (HCV).^[35] Additionally, the presence of CLIP4 as a novel self-antigen in Systemic Lupus Arythematosus points to it having a potential role in the disease mechanism.^[36]

These orthologs were chosen and organized based on estimated date of divergence from the human protein as well as the global sequence identity.^[37]