[Wormbase] hoe-1 encodes, by alternative splicing, two isoforms of a putative metal-dependent hydrolase orthologous to human ELAC2 (OMIM:605367, associated with susceptibility to prostate cancer); HOE-1 is required for fertility, normal growth progression during the late larval stages and germ line proliferation; since hoe-1(RNAi) animals do not produce gametes, hoe-1 may be required for mitosis and meiosis; hoe-1 deficiency suppresses the multivulva (Muv) phenotype of activated LET-60/RAS, while having no effect on other RAS pathway members.
Wormbase predicts 2 models, but Caenorhabditis elegans cDNA sequences in GenBank, dbEST, Trace and SRA, filtered against clone rearrangements, coaligned on the genome and clustered in a minimal non-redundant way by the manually supervised AceView program, support at least 4 spliced variants
AceView synopsis, each blue text links to tables and details
According to AceView, this gene is expressed at high level
, 2.2 times the average gene in this release, mostly from L1 larvae to adult [Kohara cDNAs]. The expression profile for the gene, derived from the proportion of animals at each stage in each Kohara library is: embryos 1%, L1 or L2 larvae 24%, L3 to adult 75%. See the in situ hybridization pattern in Kohara NextDB
. The sequence
of this gene is defined by 14 cDNA clones
and 15 elements defined by RNA-seq, some from mixed (seen 5 times), l2 (2), l1 (once). We annotate structural defects or features
in one cDNA clone.
Alternative mRNA variants and regulation:
The gene contains 9 distinct introns
(8 gt-ag, 1 other). Transcription produces at least 5 different mRNAs
, 4 alternatively spliced variants and 1 unspliced form. Variant a is transpliced to SL2, SL3, c to SL1, SL2, SL3, SL7. There are 2 probable alternative promotors
, 2 non overlapping alternative last exons and 4 validated alternative polyadenylation sites
(see the diagram
). The mRNAs appear to differ by truncation of the 3' end.
There are 3 articles
specifically referring to this gene in PubMed. This gene is associated to a phenotype
(LONg body length, SLow growth). Proteins are expected to have molecular function
(hydrolase activity) and to localize
in cytoplasm. The gene interacts
with 2 other genes (GLD-1, LET-60).
Protein coding potential:
3 spliced mRNAs putatively encode good proteins
, altogether 2 different isoforms (2 complete, 1 partial
), some containing beta-lactamase-like domain
[Pfam], a coiled coil stretch [Psort2]
. The remaining 2 mRNA variants (1 spliced, 1 unspliced; 2 partial) appear not to encode good proteins.
Please quote: AceView: a comprehensive cDNA-supported gene and transcripts annotation, Genome Biology 2006, 7(Suppl 1):S12
Map on chromosome IV, links to other databases and other names
This gene hoe-1 maps on chomosome IV at position +1.17 (interpolated). In AceView, it covers 4.79 kb
, from 4744258 to 4739474 (WS190), on the reverse strand.
Links to: WormBase
The gene is also known in Wormgenes/AceView by its positional name 4F504, in Wormbase by its cosmid.number name E04A4.4, in NextDB, the Nematode expression pattern database, as CEYK89.
Closest AceView homologs in other species
The closest human gene
, according to BlastP, is the AceView gene ELAC2
The closest mouse gene
, according to BlastP, is the AceView gene Elac2
The closest A.thaliana genes
, according to BlastP, are the AceView genes AT3G16260
Alternative mRNAs are shown aligned from 5' to 3' on a virtual genome where introns have been shrunk to a minimal length. Exon size is proportional to length, intron height reflects the number of cDNAs supporting each intron, the small numbers show the support of the introns in deep sequencing (with details in mouse-over) . Introns of the same color are identical, of different colors are different. 'Good proteins' are pink, partial or not-good proteins are yellow, uORFs are green. 5' cap or3' poly A flags show completeness of the transcript.
Mouse over the ending of each transcript gives tissues from which the supporting cDNAs were extracted. Details on tissue of origin for each intron and exon is available from the intron and exons table
Click on any transcript to open the specific mRNA page, to see the exact cDNA clone support and eventual SNPs and to get details on tissues, sequences, mRNA and protein annotations. Proteins supported by a single continuous cDNA sequence lead to underlining the name/ending of the variant. Names not underlined result from cDNA concatenation in the coding region and should be experimentally checked.
are depicted by broken lines; the height of the top of each intron reflects the relative number of clones supporting this intron. ]^[ A pink broken line
denotes an intron with standard boundaries (gt-ag or gc-ag) that is exactly supported (i.e. a cDNA sequence exactly matches the genome over 16 bp, 8 on both sides of the intron). ] ^ ] A blue broken line
denotes non-standard introns, exactly supported, but with non-standard at-ac or any other boundaries. ]-[ Pink
and ] - ] blue
straight lines represent 'fuzzy' introns of the standard and non-standard types respectively, those introns do not follow the 16 bp rule. Black straight lines ]-[denote gaps in the alignments.
Wide filled pink areas represent putative protein coding regions, narrow empty pink boxes represent the 5'UTR (on the left) and 3' UTR (on the right). Flags identify validated endings: cap site on the 5' side, polyadenylation site on the 3' side. Filled flags correspond to frequent events while empty flags have lesser supporting cDNAs (yet all are validated); at the 3' side, black flags are associated to the main AATAAA signal, blue flags
to any single letter variant of the main . More explanations are given in the gene help file