Draft:PCNX4
Submission declined on 16 August 2024 by Mgp28 (talk).
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- Comment: Almost all of the references are links to datasets. Firstly, these do not provide the type of coverage needed to demonstrate notability. Secondly, they make it very difficult to write about the gene without straying into original research. I recommend finding secondary sources about the gene to use as sources. Additional points: It's best not to number figures as they can go out of order when someone else edits the article, as has already happened. I note that you have released all the figures as your own work. I imagine this was a lot of work, but is there some assurance they are accurate? The final reference is a complete manuscript so gives more to build an article from, but again it is a primary source and the guideline on sourcing for medical topics recommends finding secondary sources. The article refers to the bottom strand -- should this be antisense strand? Mgp28 (talk) 15:45, 16 August 2024 (UTC)
Pecanex-like protein 4 (PCNX4) is a protein which in humans is encoded by the PCNX4 gene.[1]. PCNX4 is a gene expressed moderately in 27 different tissue types in humans, but most abundantly in brain, endometrium, prostate, and adrenal tissue[1]. Its likely function is a transmembrane protein in the endoplasmic reticulum[2]
Gene
[edit]PCNX4 is a protein encoding gene located on chromosome 14 in Homo sapiens at location q23.1 (see Figure 1).[3].Neighboring genes to PCNX4 are LRRC9 on the positive strand and DHRS7 on the bottom strand[1]. LRRC9 is expressed most in the testis—a leucine rich repeat; while DHRS7 a dehydrogenase/reductase is expressed most in the prostate, similar to PCNX4 [4][5].
Other names for this gene are: PCNXL4, C14orf135, Chromosome 14 open reading frame 135, Hepatitis C Virus F Protein-Binding Protein 2, and HCV F Protein-Binding Protein 2[3].
Expression
[edit]Expression of this gene can be predominately seen in the endometrium, prostate, and adrenal, but is known to be expressed in 27 total tissue types[1]. Overall, there are some clear levels of expression in reproductive tissues, brain, and GI organs seen in multiple different tissue analysis[1].
Throughout early development, the expression of PCNX4 is variable to an adult and can be as high as two-fold to normal adult expression patterns[1].
mRNA
[edit]The protein sequence of PCNX4, isoform 1, includes 15 transmembrane regions, 2 glycosylation sites, and 12 exons[6]. PCNX4 has two isoforms with isoform-1 being the longest while isoform-2 has missing exons or shorter N-terminus'[3].
Protein
[edit]The PCNX4 protein molecular weight is approximately 133 kDa with an amino acid makeup of 1,172[3][6]. The isoelectric point is 5.9[7]. The classification type is a transmembrane protein[2].
Structure
[edit]The structure of PCNX4 can be seen in figures 3 & 4. Figure 3 contains 13 beta strands and 16 alpha helices. Figure 4 contain 5 beta strands and 24 alpha helices. Both figures make up the entire human PXNC4 protein together.
Background
[edit]The evolution of the PCNX4 protein can be visualized along with cytochrome c and fibrinogen alpha as references of known evolution rates in graph 1. Cytochrome c has a small and conserved sequence compared to fibrinogen alpha which has a larger and more malleable sequence. Based on the trends provided by multiple ortholog sequences, PCNX4 illustrates a moderately evolved protein. Its sequence is fairly large, but is not as changed in terms of fibrinogen alpha.
Orthology
[edit]PCNX4 is found to have around 600 vertebrate orthologs[9]. Some additional orthologs include invertebrates such as Arachnida, Bivalvia, and Echinoidea. Orthologs are not present in land plants and bacteria.
Paralogs
[edit]An important paralog to PCNX4 is PCNX3[3]. PCNX1 and PCNX2 exists, but they are not as closely related to PCNX4. When comparing protein sequences, the four different PCNX do not align as closely as even close orthologs do, see Figure 5.
Protein sub-cellular localization
[edit]Mostly, PCNX4 is found to be in the ER, cytosol, and plasma membrane[2][11]. With no signifiant signal peptides identified, it is also congruent with being local and not traveling to areas such as the nucleus in the cell[12].
Protein analysis
[edit]PCNX4 is rich in hydrophobic amino acids, somewhat more rich than the average human protein. This is likely due to its high count of transmembrane domains[13]
Clinical significance
[edit]Current literature contains some information of PCNX4 in relation to the study of mental illness in women, such as major depressive disorder[14]. Torii et al. found that in women, for early onset major depressive disorder, expression of PCNX4 was higher due to the expression of the gene in the brain and in the reproductive tissue. The expression of PCNX4 in the tissues leads to a possible additive effect for women’s susceptibility to mental health ailments.
Conceptual translation
[edit]Conserved amino acids were determined by preservation throughout orthologs when aligned with Clustal Omega[10]. From there, 20% of the amino acids were bolded on the conceptual translation (figure 6).
References
[edit]- ^ a b c d e f "Pecanx-4 [Homo sapiens (Human)] -Gene-NCBI". National Center for Biotechnology Information, U.S. National Library of Medicine.
- ^ a b c "PCNX4 -DeepLoc". DTU Health Tec- DeepLoc.
- ^ a b c d e "PCNX4 Gene". GeneCards.
- ^ "LRRC9 leucine rich repeat containing 9 [Homo sapiens (human)]-Gene-NCBI". National Center for Biotechnology Information, U.S. National Library of Medicine.
- ^ "DHRS7B dehydrogenase/reductase 7B [Homo sapiens (human)]-Gene-NCBI". National Center for Biotechnology Information, U.S. National Library of Medicine.
- ^ a b "Pecanx-4 [Homo sapiens (Human)] -Protein NCBI". National Center for Biotechnology Information, U.S. National Library of Medicine.
- ^ "PCNX4". Expasy.
- ^ a b "I-TASSER". Protein Structure and Function Predictions.
- ^ "PCNX4 [Homo sapiens (Human)] -Orthologs -NCBI". National Center for Biotechnology Information, U.S. National Library of Medicine.
- ^ a b "Clustal Omega; Multiple Sequence Alignment". EMBL's European Bioinformatics Institute.
- ^ "PCNX4". Human Protein Atlas.
- ^ "PCNX4 -SignalP". DTU Health Tech -SignalP.
- ^ "PCNX4 SAPS". SAPS Sequence Statistics.
- ^ Torii; Ohi; Fujikane; Takai; Kuramitsu; Muto; Sugiyama; Shioiri (2024-06-07). "Tissue-specific gene expression of genome-wide significant loci associated with major depressive disorder subtypes". Progress in Neuropsychopharmacology & Biological Psychiatry. 133: 7. doi:10.1016/j.pnpbp.2024.111019. PMID 38663672 – via ELSEVIER.
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