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. 2017 Oct 3;2017:10.17912/W2CQ14. doi: 10.17912/W2CQ14

Novel deletion alleles of a C. elegans gene Y48E1C.1, named as tm5468, tm5625 and tm5626

Sayaka Hori 1, Yuji Suehiro 1, Sawako Yoshina 1, Shohei Mitani 1,§
Reviewed by: James Lee
PMCID: PMC7255877  PMID: 32550357

Figure 1.

Figure 1.

Figure 1. Location of the novel alleles

Description

We report tm5468, tm5625 and tm5626 as novel deletion alleles of the gene Y48E1C.1 that is the only ortholog of human calmodulin-lysine N-methyltransferase (CAMKMT)1. CAMKMT encodes an evolutionarily conserved enzyme class I protein methyltransferase that acts in the formation of trimethyllysine in calmodulin for calcium-dependent signaling2. CAMKMT mutation is associated with Hypotonia-cystinuria syndrome in human2,3. The alleles were isolated from the comprehensive screening of gene deletions generated by TMP/UV4. In the screening, all the alleles were detected by nested PCR using the following primer sets, 5’- TCAAGCCACGCCCACACTTA-3’ and 5’- GAAGGCATACAGTGGGGGTA-3’ for the first round PCR and 5’- CGCCCACACTTAATGGTTAT-3’ and 5’- GGGCAGTGTAGGGATACTGT-3’ for the second round PCR. By Sanger sequencing, the 30 bp flanking sequences of the alleles tm5468, tm5625 and tm5626 were identified as AATCCTTCACACACCACAACAGAAATCCTA – [384 bp deletion] -CGAGGTCACGCCCACACATTGGGCGGAGTT, CCGATGCTCCGTGCTGCTCCAAGTGCTCCG – [627 bp deletion + 9 bp insertion (TAATCTTGT)] – AGTACTCCTACAGTATCCCTACACTGCCCC, and AAAAAAGGATGACGTCACAGTTGCTCCGAT – [256 bp deletion] – ACGCCGATTCGGCAGCCGAATGATCTACAG, respectively. Based on the information about the splicing isoforms of Y48E1C.1 (WormBase, http://www.wormbase.org, WS259), the forth exon of Y48E1C.1a, Y48E1C.1b (annotated as non cording RNA) and the second exon of Y48E1C.1d transcripts are deleted in tm5468, tm5625 and tm5626(Fig. 1). Presumably, all of the alleles do not affect Y48E1C.1c. According to information of protein in Wormbase, this exon contains a predicted some motif, suggesting hypothetical functional deficiency of Y48E1C.1aY48E1C.1b, and Y48E1C.1d in the deletion mutants. In addition, these alleles are expected to be usable for comparing functions among the isoform c and the other isoforms. However, no visually obvious phenotypes (Let, Unc, and Dpy) were observed in tm5468, tm5625 and tm5626.

Reagents

FX05468 Y48E1C.1 (tm5468) II (Not outcrossed)

FX05625 Y48E1C.1 (tm5625) II (Not outcrossed)

FX05626 Y48E1C.1 (tm5626) II (Not outcrossed)

Acknowledgments

Funding

The National BioResource Project.

References

  1. Magnani R, Dirk LM, Trievel RC, Houtz RL. Calmodulin methyltransferase is an evolutionarily conserved enzyme that trimethylates Lys-115 in calmodulin. Nat Commun. 2010 Jul 27;1:43–43. doi: 10.1038/ncomms1044. [DOI] [PubMed] [Google Scholar]
  2. Magen S, Magnani R, Haziza S, Hershkovitz E, Houtz R, Cambi F, Parvari R. Human calmodulin methyltransferase: expression, activity on calmodulin, and Hsp90 dependence. PLoS One. 2012 Dec 20;7(12):e52425–e52425. doi: 10.1371/journal.pone.0052425. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. Bartholdi D, Asadollahi R, Oneda B, Schmitt-Mechelke T, Tonella P, Baumer A, Rauch A. Further delineation of genotype-phenotype correlation in homozygous 2p21 deletion syndromes: first description of patients without cystinuria. Am J Med Genet A. 2013 Jun 21;161A(8):1853–1859. doi: 10.1002/ajmg.a.35994. [DOI] [PubMed] [Google Scholar]
  4. Gengyo-Ando K, Mitani S. Characterization of mutations induced by ethyl methanesulfonate, UV, and trimethylpsoralen in the nematode Caenorhabditis elegans. Biochem Biophys Res Commun. 2000 Mar 01;269(1):64–69. doi: 10.1006/bbrc.2000.2260. [DOI] [PubMed] [Google Scholar]

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