The most common aliases for GOLGA8H are the following:1
GOLGA8H, when compared to many other genes, exists in many different places that span multiple chromosomes:.2 NCBI lists the gene’s location on the long (q) arm on Chromosome 15 in the q13.2 region, from 30,604,030 - 30,617,827 (13,798 nt in length)3
In actuality, when running the FASTA protein sequence of GOLGA8H on BLAT (the BLAST-Like Alignment Tool), it is found to exist in 85 or 87 different locations (depending on an individual’s sex chromosomes).4 81 copies of the protein exist on chromosome 15, one copy each on chromosomes 7, 9,10, and 12, and two copies on the Y chromosome5
Copies of GOLGA8H in Homo Sapiens
It would be tedious and inefficient to list all gene neighborhoods for the 87 locations of GOLGA8H. Thus, here are surrounding genes of GOLGA8H on chromosome 15 in the q13.2 region listed on NCBI:6
Gene Neighborhood of GOLGA8H on Chromosome 15 q13.2 in Homo sapiens7:
There are no isoforms of GOLGA8H.8
A multiple sequence alignment (MSA) of GOLGA8H and its top seven paralogs was created using Clustal Omega [1]. [Appendix A] All eight genes from the Golgin Subfamily A Member 8 group were 632 amino acids in length [1]. All 632 amino acids of GOLGA8H and its top seven paralogs were analyzed and compared using Clustal Omega were analyzed and compared in an attempt to understand what makes Golgin Subfamily A Member 8H, GOLGA8H, a distinct entity. Two amino acids make GOLGA8H unique: Valine at amino acid 32 and Cysteine at amino acid 169.9 For all seven paralogs, the amino acid in position 32 is Isoleucine and the amino acid in position 169 is Arginine10
The predicted molecular weight of GOLGA8H, rounded down to three significant figures, is 71.3 kDa.11 This is a theoretical value; predicted molecular weights are merely based on the amino acids present in the protein. The theoretical isoelectric point of GOLGA8H, rounded down to one significant figure, is a pI of 812
When compared to other human proteins, GOLGA8H is semi glutamine- and glutamate-enriched.13 In contrast, GOLGA8H is depleted in threonine, phenylalanine, and tyrosene.14
There are no charge runs, hydrophobic segments, or transmembrane domains in the GOLGA8H protein.15 There are 62 amino acid multiplets for the protein, which is higher than the expected range.16 It also has amino acid patterns with high periodicity17
There are 11 motifs present in GOLGA8H:.18 The single experimentally-verified motif is a glutamine-rich protein located in the 323-416 amino acid region.
GOLGA8H is predicted to undergo phosphorylation at multiple locations of serine, threonine, and tyrosine throughout its structure.20 It is expected to undergo phosphorylation most frequently on serine amino acids.21 Furthermore, there is one predicted N-linked glycosylation site, which occurs at amino acid 39.22 The sequence for this site is NGS.23 N-linked glycosylation functions intrinsically and extrinsically to assist in regulating the migration patterns of cells.24
The protein is 632 amino acids long.25 It has 19 exons and two polyadenylation signals.26 Its sequence only partially matches a Kozak consensus sequence.27
The predicted secondary structure of GOLGA8H is composed of 81% alpha helices, 25.6% beta sheets, and 17.2% turns.28
Using Phyre2, 284 residues (45% of GOLGA8H) was modeled with 97.8% confidence by the single highest scoring template.29 This structure shows an extremely high proportion of alpha helices:30
A predicted model for a tertiary structure of GOLGA8H was generated using I-TASSER31
There is one promoter for the GOLGA8H gene, GXP_2235212, which is 1197 nt long.32 It lies from base pairs 30,603,030 to 30,604,226 on the positive strand33
Several transcription factors are predicted to bind to the promoter sequence. Some examples include:34
GOLGA8H has several dozen paralogs. There are seven paralogs with identity similarities above 90%, charted below under GOLGA8H (included as a reference point):35
Putting the amino acid sequence of GOLGA8H through a protein BLAST via NCBI does not yield any hits for orthologs:.37 However, putting the same sequence through BLAT (the BLAST-Like Alignment Tool) yields multiple orthologs38
**Chromosomes labeled as 'uncharacterized' have clone contigs (an assembled set of overlapping DNA sequences) that cannot be confidently placed on a specific chromosome. Similar contigs are concatenated together into short pseudo-chromosomes.
Data from NCBI shows that GOLGA8H in Homo sapiens has the strongest expression is through the thyroid and testis, with RKPMs of 12.2 and 12.1 respectively. It is also expressed in lesser amounts in 25 other tissues.40 Data from GEO DataSet show the tissue expression is highest in bone marrow and pancreas tissue.41 However, samples from all tissues were above the 90th percentile, indicating that the expression value of that gene is much higher in respect to all other genes on the array.42
When comparing GOLGA8H tissue expression in abnormal conditions to normal human tissue levels, there is not significant deviation in its expression with any variable.43 This supports the notion that GOLGA8H is ubiquitous.
GOLGA8H has been shown to interact with Ubiquitin C (UBC).44 UBC is a polyubiquitin precursor. Polyubiquitin precursors are a chain of the protein ubiquitin that can be turned into an active form by post-translational modifications. This can mark proteins for degradation, alter their cellular location, affect their activity, and promote or prevent protein interactions. Further research on the link between ubiquitin and the Golgi apparatus include a reliance on ubiquitin to achieve certain processes around the Golgi apparatus.4546
String db lists the following genes as interacting with GOLGA8H:47
The Homo sapiens GOLGA8H gene has 1 splice variant49
"GOLGA8H golgin A8 family member H [Homo sapiens (human)] - Gene - NCBI". www.ncbi.nlm.nih.gov. Retrieved 2019-02-24. https://www.ncbi.nlm.nih.gov/gene/728498 ↩
"BLAT Search: GOLGA8H". genome.ucsc.edu. Retrieved 2019-05-13. https://genome.ucsc.edu/cgi-bin/hgBlat ↩
"GOLGA8H golgin A8 family member H [ Homo sapiens (human) ]". National Center for Biotechnology Information. https://www.ncbi.nlm.nih.gov/gene/?term=GOLGA8H ↩
"Clustal Omega < Multiple Sequence Alignment < EMBL-EBI". www.ebi.ac.uk. Retrieved 2019-05-15. https://www.ebi.ac.uk/Tools/msa/clustalo/ ↩
"ExPASy". web.expasy.org. Retrieved 2019-05-13. https://web.expasy.org/cgi-bin/compute_pi/pi_tool1?P0CJ92@1-632@average ↩
"SAPS < Sequence Statistics < EMBL-EBI". www.ebi.ac.uk. Retrieved 2019-05-13. https://www.ebi.ac.uk/Tools/seqstats/saps/ ↩
"PROSITE". prosite.expasy.org. Retrieved 2019-05-13. https://prosite.expasy.org/PDOC50099 ↩
"NetPhos 3.1 Server". www.cbs.dtu.dk. Retrieved 2019-05-15. http://www.cbs.dtu.dk/services/NetPhos/ ↩
Taylor ME (2006). Introduction to glycobiology. Drickamer, Kurt. (2nd ed.). Oxford: Oxford University Press. ISBN 0199282781. OCLC 62307306. 0199282781 ↩
"CFSSP: Chou & Fasman Secondary Structure Prediction Server". www.biogem.org. Retrieved 2019-05-13. http://www.biogem.org/tool/chou-fasman/index.php ↩
"Phyre 2 Results for GOLGA8H". www.sbg.bio.ic.ac.uk. Retrieved 2019-05-13. http://www.sbg.bio.ic.ac.uk/phyre2/html/page.cgi?id=index ↩
"I-TASSER results". zhanglab.ccmb.med.umich.edu. Archived from the original on 2019-05-13. Retrieved 2019-05-13. https://web.archive.org/web/20190513040532/https://zhanglab.ccmb.med.umich.edu/I-TASSER/output/S461042/ ↩
"Genomatix: Gene2Promoter". www.genomatix.de. Archived from the original on 2022-11-27. Retrieved 2019-05-14. https://web.archive.org/web/20221127070551/https://www.genomatix.de/cgi-bin/sessions/login.pl?s=9797c94d2d4215749ea3f9fb93846a37 ↩
"TimeTree :: The Timescale of Life". timetree.org. Retrieved 2019-05-15. http://timetree.org/ ↩
"About GEO Profiles - GEO - NCBI". www.ncbi.nlm.nih.gov. Retrieved 2019-05-13. https://www.ncbi.nlm.nih.gov/geo/info/profiles.html ↩
"Gene Set - GOLGA8H". amp.pharm.mssm.edu. Retrieved 2019-02-24. http://amp.pharm.mssm.edu/Harmonizome/gene_set/GOLGA8H/Pathway+Commons+Protein-Protein+Interactions ↩
Alberts B, Johnson A, Lewis J, Raff M, Roberts K, Walter P (2002). Molecular Biology of the Cell (4th ed.). Garland Science. ISBN 9780815332183. 9780815332183 ↩
Glickman MH, Ciechanover A (April 2002). "The ubiquitin-proteasome proteolytic pathway: destruction for the sake of construction". Physiological Reviews. 82 (2): 373–428. doi:10.1152/physrev.00027.2001. PMID 11917093. /wiki/Doi_(identifier) ↩
"STRING: functional protein association networks". string-db.org. Retrieved 2019-05-15. https://string-db.org/ ↩
"Gene: GOLGA8H (ENSG00000261794) - Splice variants - Homo sapiens - Ensembl genome browser 95". useast.ensembl.org. Retrieved 2019-03-04. http://useast.ensembl.org/Homo_sapiens/Gene/Splice?db=core;g=ENSG00000261794;r=15:30604126-30614561;t=ENST00000566740 ↩