Jump to content

ZSWIM9

From Wikipedia, the free encyclopedia

Zinc finger SWIM-type containing 9 is a protein encoded in humans by the ZSWIM9 gene.[1] It is a member of zinc finger SWIM-type family. This gene is expressed in embryonic development and predicted to act in cell differentiation.[2]

Zinc finger SWIM-type containing 9
Tertiary structure of ZSWIM9
Tertiary structure of ZSWIM9 rainbow colored from N-terminus to C-terminus
Identifiers
SymbolZSWIM9
Alt. namesc19orf68
HGNC34495
RefSeqNM_199341.4
UniProtQ86XI8
Other data
LocusChr. 19 q13.33
Search for
StructuresSwiss-model
DomainsInterPro

Gene

[edit]

The ZSWIM9 gene is located on the plus strand at 19q13.33 from 48,170,680 to 48,197,620 spanning 26,941 base pairs.[3] Also known as C19orf68, this gene has orthologs in placental mammals, marsupials, reptiles (turtles), birds (flightless birds), and amphibians.[4] ZSWIM9 has 4 exons, with variation between isoforms.

mRNA and transcriptional variants

[edit]

Transcripts

[edit]
DNA sequences of ZSWIM9 transcript variants with their exons labeled. Transcript variant 1 is labeled with a red box. Each exon (1-4) is labeled above, as well as the other variants.

ZSWIM9 has a total of six transcriptional variants with isoform 1 being the most complete and understood.[1] All isoforms contain a conserved domain, FAR1, except X3 and X5, as well as the SWIM-type domain.

Transcript variants of ZSWIM9
Transcript Variant Accession number mRNA length (nucelotides) Protein length

(amino acids)

Molecular weight (kDa)
1 NM_199341.4 3600 920 101.7
X1 XM_006723204.4 3914 947 104.6
X2 XM_005259449.4 4281 933 103.2
X3 XM_006723205.3 3596 920 101.6
X4 XM_011526936.3 3624 848 93.1
X5 XM_047438788.1 3130 720 80.0
Exons present in each isoform of ZSWIM9
Isoform Exon 1 Exon 2 Exon 3 Exon 4
1 ✓ ✓ ✓ ✓
X1 ✓ ✓ ✓ ✓
X2 ✓ ✓ ✓ ✓
X3 ✓ ✓ ✓ ✓
X4 x x ✓ ✓
X5 x x x ✓

Protein

[edit]

The human ZSWIM9 protein is 920 amino acids long with a molecular weight of 101.7 kDA and a theoretical isoelectric point of 8.51.[5]

Composition

[edit]

The human ZSWIM9 protein along with orthologs has higher than normal amounts of arginine, specifically around amino acids 379-421.[6] Arginine has been seen to play a crucial role in genome stability[7] and typically associated with interactions with nucleic acids, specific cellular localization (nucleus), or involvement in structural or enzymatic roles. The high concentration of arginine residues influences the protein's charge, binding properties, and potential regulatory functions. Arginine-rich proteins can play crucial roles in cell differentiation during embryonic development due to their involvement in processes that regulate gene expression, chromatin remodeling, and signaling pathways.[8]

Conserved domains/motifs

[edit]
Multiple sequence alignment (MSA) of ZSWIM9 and its close orthologs, specifically showing the conserved FAR1 domain from amino acids 97-128.

ZSWIM9 contains a zinc finger SWIM-type profile, a pattern recognized in human protein ZSWIM9 and its orthologs that represent a shared zinc-binding motif.[9][10] The acronym "SWIM" stands for SWI2/SNF2 and MuDR and detects conserved cysteine- and histidine-rich regions involved in zinc coordination, which facilitates protein-DNA or protein-protein interactions.

There is a conserved FAR1 DNA-binding domain from amino acids 97-128.[6] This indicates that ZSWIM9, a member of the FRS family, shares a domain architecture with mutator-like transposases, including an N-terminal C2H2 zinc finger domain, a central transposase-like domain, and a C-terminal SWIM motif. This structure, coupled with its FAR1-like DNA-binding domain, suggests ZSWIM9 functions as a transcriptional regulator, potentially co-opted from transposases to play roles in gene expression, DNA repair, or transposon splicing.[11]

Schematic illustration of human protein ZSWIM9 with important domains, motifs, and post-translational modifications identified.

There is a family of unknown function (DUF5575) from amino acids 12-320.[12]

Regulation

[edit]

Gene level regulation

[edit]

Located in the nucleoplasm,[13] ZSWIM9 in humans is ubiquitously expressed in medium abundance in the brain (fetal brain, and cerebellum), fat, and kidneys.[14][15] Ubiquitously expressed, with some variability, in low abundance in early developed fetal hearts and fetal lungs.[16]

While ZSWIM9 is expresses in low levels among fetal hearts, it has been predicted that there is a higher expression in earlier developed embryoid stem cells and embryoid bodies with beating cardiomyocytes, then a decreased level of expression later on in development such as in mature cardiomyocytes from fetal hearts.[17] This suggests ZSWIM9 might play a role in early differentiation stages and cellular commitment processes.

Additionally, higher expression of ZSWIM9 was seen in myotonic dystrophy type 2, which is muscle dysfunction in numerous muscle types including cardiac,[18] compared to a control from DM2 vastus lateralis muscle tissue.[19] Higher expression suggests that ZSWIM9 may have a role in the muscle’s response to chronic disease-related stress, regeneration process, or damage repair. This pattern of expression may reflect ZSWIM9’s involvement in cellular pathways that become more active or dysregulated in the disease state.

Protein level regulation

[edit]

The human ZSWIM9 protein is predicted to be primarily localized in the nucleus[20] and cytoplasm,[21] however, it has also been visualized via immunofluorescence in the nucleoplasm.[22] It was also predicted ZSWIM9 has nuclear export signals, which direct proteins from the nucleus to the cytoplasm.[23] The presence of an NES indicates the protein may shuttle between the nucleus and cytoplasm, depending on cellular conditions or specific signals (e.g., stress, phosphorylation).

Phosphorylation

Interacting proteins

[edit]

ZSWIM9 was found to primarily interact with proteins involved with DNA maintenance in the nucleus, cytoplasm, and nucleoplasm.[24]

ZSWIM9 interacting proteins
Protein Detection method Subcellular localization Function
Chromobox protein homolog 1 Tandem affinity purification Nucleus, nucleoplasm, chromosome, cytoskeleton Component of heterochromatin. Recognizes and binds histone H3 tails methylated at 'Lys-9', leading to epigenetic repression. Interaction with lamin B receptor (LBR) can contribute to the association of the heterochromatin with the inner nuclear membrane.
BMI1 (Polycomb complex protein) Co-immunoprecipitation Nucleus, nucleoplasm, chromosome, cytosol Component of a Polycomb group (PcG) multiprotein PRC1-like complex, a complex class required to maintain the transcriptionally repressive state of many genes, including Hox genes, throughout development.
CBX3

(Chromobox 3)

Co-immunoprecipitation Nucleus, nuclear envelope, nucleoplasm, chromosome, cytoskeleton Seems to be involved in transcriptional silencing in heterochromatin-like complexes. Recognizes and binds histone H3 tails methylated at 'Lys-9', leading to epigenetic repression. May contribute to the association of the heterochromatin with the inner nuclear membrane through its interaction with the lamin B receptor (LBR).
FHL3 (Human four-and-a-half LIM-only protein 3) Co-immunoprecipitation Nucleus, cytoskeleton Recruited by SOX15 to FOXK1 promoters where it acts as a transcriptional coactivator of FOXK1.

Histone 3 (H3) is an arginine-rich histone and is linked active chromatin structures and gene activation.[25]

Hox genes are a group of related genes that play a critical role in the development and organization of an organism's body plan during embryonic development.[26] This is indicative of ZSWIM9 protein function.

SOX15 binds to the DNA consensus sequence 5'-AACAATG-3' and can function as both an activator and repressor. It synergistically interacts with POU5F1 (OCT3/4) at gene promoters and activates the FOXK1 promoter by recruiting FHL3, promoting myoblast proliferation. Additionally, it inhibits myoblast differentiation by repressing muscle-specific genes like MYOD and MYOG.[27]

Evolution

[edit]
Phylogenetic tree showing the evolutionary history of ZSWIM9 protein in humans and its orthologs. Each circle shows taxonomic groups represented by orthologs found in table 1. Some orthologs were not including due to crowding, but each taxonomic group within the twenty orthologs of ZSWIM9 is represented.

Paralogs

[edit]

ZSWIM9 has paralogs in ZSWIM1-8 as it is apart of the zinc finger SWIM-type gene family and the SWIM domain is conserved throughout. However, it's two closely conserved paralogs are ZSWIM1 and ZSWIM3.[1]

Orthologs

[edit]

Orthologs of ZSWIM9 were found in placental mammals, marsupials, reptiles, birds, and amphibians.[4] ZSWIM9 is found in reptiles, but only in turtles and in birds, but only in flightless birds. This could indicate a key point of divergence or a result of ZSWIM9 protein function.[28]

Graph of the estimated date of divergence linearly, based on ZSWIM9 compared to Cytochrome C and Fibrinogen Alpha. ZSWIM9 mutates faster than Cytochrome C but not faster than Fibrinogen Alpha. The ZSWIM gene family likely appeared around 350 million years ago due to the fact that it doesn’t have known orthologs before amphibians.
Selected Orthologs of ZSWIM9
Organism type Species name Common name Taxonomic group Date of divergence (MYA) % Identity % Similarity AC# Protein length
Placental Homo sapiens Human Primate 0 100 100 NP_955373 920
Oryctolagus cuniculus Rabbit Lagomorpha 87 69 73 XP_051693391 913
Mus musculus House mouse Rodentia 87 67.9 74.2 NP_796286.2 849
Camelus ferus Wild Bactrian camel Artiodactyla 94 85.4 89.2 XP_032341552.1 923
Vulpes lagopus Arctic fox Carnivora 94 84.8 69.6 XP_041600653 915
Equus przewalskii Przewalski's horse Perissodactyla 94 47.8 51.4 XP_008525788 611
Marsupial Trichosurus vulpecula Common brushtail possum Diprotodotia 160 80.2 48.1 XP_036599503.1 717
Vombatus ursinus Common wombat Diprotodotia 160 75.6 65.2 XP_027715069.1 966
Antechinus flavipes Yellow-footed antechinus Dasyuromorphia 160 74.4 56.2 XP_051845809 898
Sarcophilus harrisii Tasmanian devil Dasyuromorphia 160 74.3 62.7 XP_031817585 1030
Reptile Dermochelys coriacea Leatherback sea turtle Testudines 319 61.9 43.2 XP_043357605.1 538
Emydura macquarii Murrey river turtle Testudines 319 61.8 43.6 XP_067413334.1 538
Bird Rhea pennata Darwin's rhea Rheiformes 319 44.2 33.5 XP_062449005.1 535
Apteryx rowi Okarito kiwi Apterygiformes 319 43.3 33.4 XP_025945372.1 535
Dromaius novaehollandiae Emu Palaeognathae 319 43.1 33.5 XP_025976311.1 535
Amphibian Rhinatrema bivittatum Two-lined caecilian Gymnophiona 352 51.9 39.7 XP_029440252.1 548
Geotrypetes seraphini Gaboon caecilian Gymnophiona 352 50.1 38.5 XP_038816602.1 548
Microcaecilia unicolor Tiny cayenne caecilian Gymnophiona 352 50 38.5 XP_030053572.1 544
Ascaphus truei Coastal tailed frog Anura 352 49.3 38.3 MEE6483311.1 536
Ambystoma mexicanum Axolotl Urodela 352 46.9 36.6 XP_069493689.1 544
Pleurodeles waltl Iberian ribbed newt Urodela 352 45.8 34.9 XP_069056600.1 580

Function

[edit]

Zinc-finger proteins contain a short finger-like structural motif stabilized by zinc-ions [1] which are involved in critical biological processes including cell differentiation[29] and embryonic development.[30] ZSWIM9, however, is classified by the SWIM domain, characterized by a CxCxnCxH molecular structure.[2] The SWIM domain is predicted to have DNA-binding and protein-protein interaction functions.[31]

Clinical significance

[edit]

A couple of single nucleotide polymorphisms (SNPs) were identified as clinically significant and associated with ZSWIM9.[32] One study associate a SNP in ZSWIM9 with acute Graft versus Host Disease (aGvHD) which affects patients undergoing allogeneic hematopoietic stem-cell transplantation (allo-HSCT). This condition is triggered by the damage to normal tissue caused by pre-transplant conditioning regimens, with DNA-repair mechanisms potentially playing a key role in mitigating this damage.[33] This could be associated with proteins involved in cell differentiation through several mechanisms related to DNA repair, gene expression regulation, and cellular responses to stress or injury.

An additional SNP was identified with ZSWIM9 and associated with body height.[34]

References

[edit]
  1. ^ a b c "ZSWIM9 zinc finger SWIM-type containing 9 [Homo sapiens (human)] - Gene - NCBI". www.ncbi.nlm.nih.gov. Retrieved 2024-12-04.
  2. ^ a b Hassan, Imtiaz Ul; Rehman, Hafiz Mamoon; Liu, Ziran; Zhou, Liangji; Samma, Muhammad Kaleem; Wang, Chengdong; Rong, Zixin; Qi, Xufeng; Cai, Dongqing; Zhao, Hui (2023-05-18). "Genome-wide identification and spatiotemporal expression profiling of zinc finger SWIM domain-containing protein family genes". Zoological Research. 44 (3): 663–674. doi:10.24272/j.issn.2095-8137.2022.418. ISSN 2095-8137. PMC 10236294. PMID 37161653.
  3. ^ "ZSWIM9 Gene - Zinc Finger SWIM-Type Containing 9". GeneCards. December 10, 2024.
  4. ^ a b "BLAST: Basic Local Alignment Search Tool". blast.ncbi.nlm.nih.gov. Retrieved 2024-12-11.
  5. ^ "Expasy - Compute pI/Mw tool". web.expasy.org. Retrieved 2024-12-11.
  6. ^ a b "Motif Scan". myhits.sib.swiss. Retrieved 2024-12-11.
  7. ^ Sanchez-Bailon, Maria Pilar; Choi, Soo-Youn; Dufficy, Elizabeth R.; Sharma, Karan; McNee, Gavin S.; Gunnell, Emma; Chiang, Kelly; Sahay, Debashish; Maslen, Sarah; Stewart, Grant S.; Skehel, J. Mark; Dreveny, Ingrid; Davies, Clare C. (2021-11-02). "Arginine methylation and ubiquitylation crosstalk controls DNA end-resection and homologous recombination repair". Nature Communications. 12 (1): 6313. Bibcode:2021NatCo..12.6313S. doi:10.1038/s41467-021-26413-6. ISSN 2041-1723. PMC 8564520. PMID 34728620.
  8. ^ Lee, Yun Hwa; Ma, Hui; Tan, Tuan Zea; Ng, Swee Siang; Soong, Richie; Mori, Seiichi; Fu, Xin-Yuan; Zernicka-Goetz, Magdalena; Wu, Qiang (2012-09-20). "Protein Arginine Methyltransferase 6 Regulates Embryonic Stem Cell Identity". Stem Cells and Development. 21 (14): 2613–2622. doi:10.1089/scd.2011.0330. ISSN 1547-3287. PMC 5729635. PMID 22455726.
  9. ^ Makarova, Kira S.; Aravind, L.; Koonin, Eugene V. (August 2002). "SWIM, a novel Zn-chelating domain present in bacteria, archaea and eukaryotes". Trends in Biochemical Sciences. 27 (8): 384–386. doi:10.1016/s0968-0004(02)02140-0. ISSN 0968-0004. PMID 12151216.
  10. ^ "Gene group | HUGO Gene Nomenclature Committee". www.genenames.org. Retrieved 2024-12-11.
  11. ^ "InterPro". www.ebi.ac.uk. Retrieved 2024-12-11.
  12. ^ "uncharacterized protein ZSWIM9 [Homo sapiens] - Protein - NCBI". www.ncbi.nlm.nih.gov. Retrieved 2024-12-11.
  13. ^ "ZSWIM9 protein expression summary - The Human Protein Atlas". www.proteinatlas.org. Retrieved 2024-12-11.
  14. ^ Fagerberg, Linn; Hallström, Björn M.; Oksvold, Per; Kampf, Caroline; Djureinovic, Dijana; Odeberg, Jacob; Habuka, Masato; Tahmasebpoor, Simin; Danielsson, Angelika; Edlund, Karolina; Asplund, Anna; Sjöstedt, Evelina; Lundberg, Emma; Szigyarto, Cristina Al-Khalili; Skogs, Marie (February 2014). "Analysis of the human tissue-specific expression by genome-wide integration of transcriptomics and antibody-based proteomics". Molecular & Cellular Proteomics: MCP. 13 (2): 397–406. doi:10.1074/mcp.M113.035600. ISSN 1535-9484. PMC 3916642. PMID 24309898.
  15. ^ Duff, Michael O.; Olson, Sara; Wei, Xintao; Garrett, Sandra C.; Osman, Ahmad; Bolisetty, Mohan; Plocik, Alex; Celniker, Susan E.; Graveley, Brenton R. (2015-05-21). "Genome-wide identification of zero nucleotide recursive splicing in Drosophila". Nature. 521 (7552): 376–379. Bibcode:2015Natur.521..376D. doi:10.1038/nature14475. ISSN 1476-4687. PMC 4529404. PMID 25970244.
  16. ^ Szabo, Linda; Morey, Robert; Palpant, Nathan J.; Wang, Peter L.; Afari, Nastaran; Jiang, Chuan; Parast, Mana M.; Murry, Charles E.; Laurent, Louise C.; Salzman, Julia (2015-06-16). "Statistically based splicing detection reveals neural enrichment and tissue-specific induction of circular RNA during human fetal development". Genome Biology. 16 (1): 126. doi:10.1186/s13059-015-0690-5. ISSN 1474-760X. PMC 4506483. PMID 26076956.
  17. ^ "GDS3513 / 3394". www.ncbi.nlm.nih.gov. Retrieved 2024-12-13.
  18. ^ Schoser, Benedikt (2020-03-19), "Myotonic Dystrophy Type 2", GeneReviews® [Internet], University of Washington, Seattle, PMID 20301639, retrieved 2024-12-13
  19. ^ "GDS5276 / ILMN_1792828". www.ncbi.nlm.nih.gov. Retrieved 2024-12-13.
  20. ^ "DeepLoc-2.0". services.healthtech.dtu.dk. Retrieved 2024-12-13.
  21. ^ "PSORT II Prediction". psort.hgc.jp. Retrieved 2024-12-13.
  22. ^ "Search: ZSWIM9 - The Human Protein Atlas". www.proteinatlas.org. Retrieved 2024-12-13.
  23. ^ Xu, Darui; Farmer, Alicia; Collett, Garen; Grishin, Nick V.; Chook, Yuh Min (2012-09-15). Weis, Karsten (ed.). "Sequence and structural analyses of nuclear export signals in the NESdb database". Molecular Biology of the Cell. 23 (18): 3677–3693. doi:10.1091/mbc.e12-01-0046. ISSN 1059-1524. PMC 3442415. PMID 22833565.
  24. ^ "PSICQUIC View". www.ebi.ac.uk. Retrieved 2024-12-13.
  25. ^ Di Lorenzo, Alessandra; Bedford, Mark T. (2011). "Histone arginine methylation". FEBS Letters. 585 (13): 2024–2031. Bibcode:2011FEBSL.585.2024D. doi:10.1016/j.febslet.2010.11.010. ISSN 1873-3468. PMC 3409563. PMID 21074527.
  26. ^ "Hox Genes in Development: The Hox Code | Learn Science at Scitable". www.nature.com. Retrieved 2024-12-13.
  27. ^ "UniProt". www.uniprot.org. Retrieved 2024-12-13.
  28. ^ Matsuda, Yoichi; Nishida-Umehara, Chizuko; Tarui, Hiroshi; Kuroiwa, Asato; Yamada, Kazuhiko; Isobe, Taku; Ando, Junko; Fujiwara, Atushi; Hirao, Yukako; Nishimura, Osamu; Ishijima, Junko; Hayashi, Akiko; Saito, Toshiyuki; Murakami, Takahiro; Murakami, Yasunori (2005-08-01). "Highly conserved linkage homology between birds and turtles: Bird and turtle chromosomes are precise counterparts of each other". Chromosome Research. 13 (6): 601–615. doi:10.1007/s10577-005-0986-5. ISSN 1573-6849. PMID 16170625.
  29. ^ Powell, Michael D.; Read, Kaitlin A.; Sreekumar, Bharath K.; Oestreich, Kenneth J. (2019-06-06). "Ikaros Zinc Finger Transcription Factors: Regulators of Cytokine Signaling Pathways and CD4+ T Helper Cell Differentiation". Frontiers in Immunology. 10: 1299. doi:10.3389/fimmu.2019.01299. ISSN 1664-3224. PMC 6563078. PMID 31244845.
  30. ^ Close, Renaud; Toro, Sabrina; Martial, Joseph A.; Muller, Marc (2002-10-01). "Expression of the zinc finger Egr1 gene during zebrafish embryonic development". Mechanisms of Development. 118 (1): 269–272. doi:10.1016/S0925-4773(02)00283-6. hdl:2268/13012. ISSN 0925-4773. PMID 12351200.
  31. ^ Makarova, Kira S; Aravind, L; Koonin, Eugene V (2002-08-01). "SWIM, a novel Zn-chelating domain present in bacteria, archaea and eukaryotes". Trends in Biochemical Sciences. 27 (8): 384–386. doi:10.1016/S0968-0004(02)02140-0. ISSN 0968-0004. PMID 12151216.
  32. ^ "Variation Viewer". www.ncbi.nlm.nih.gov. Retrieved 2024-12-13.
  33. ^ Uppugunduri, C. R. S.; Huezo-Diaz Curtis, P.; Nava, T.; Rezgui, M. A.; Mlakar, V.; Mlakar, S. Jurkovic; Waespe, N.; Théoret, Y.; Gumy-Pause, F.; Bernard, F.; Chalandon, Y.; Boelens, J. J.; Bredius, R. G. M.; Dalle, J. H.; Nath, C. (February 2022). "Association study of candidate DNA-repair gene variants and acute graft versus host disease in pediatric patients receiving allogeneic hematopoietic stem-cell transplantation". The Pharmacogenomics Journal. 22 (1): 9–18. doi:10.1038/s41397-021-00251-7. ISSN 1470-269X. PMC 8794787. PMID 34711928.
  34. ^ Yengo, Loïc; Vedantam, Sailaja; Marouli, Eirini; Sidorenko, Julia; Bartell, Eric; Sakaue, Saori; Graff, Marielisa; Eliasen, Anders U.; Jiang, Yunxuan; Raghavan, Sridharan; Miao, Jenkai; Arias, Joshua D.; Graham, Sarah E.; Mukamel, Ronen E.; Spracklen, Cassandra N. (2022-10-27). "A saturated map of common genetic variants associated with human height". Nature. 610 (7933): 704–712. Bibcode:2022Natur.610..704Y. doi:10.1038/s41586-022-05275-y. ISSN 0028-0836. PMC 9605867. PMID 36224396.
Retrieved from "https://wiki.riteme.site/w/index.php?title=ZSWIM9&oldid=1265736866"