Structure, spatial, and temporal expression of two sea urchin metallothionein genes, SpMTB1 and SpMTA
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The metallothionein-B genes of the sea urchin Strongylocentrotus purpuratus encode a metallothionein (MT) isoform distinguishable from the MTA isoform. The MTB subfamily consists of at least two genes, MTB1 and MTB2, and possibly two to three others. The unique MTB1 and MTA genes have a high degree of identity but diverge in structural detail and expression. Transcripts of the MTA, MTB1, troponin C Spec 1, and CyIIIa actin genes begin simultaneously to accumulate at an early blastula stage. MTB1 mRNA becomes localized in the embryonic gut and oral ectoderm, whereas MTA, Spec 1, and CyIIIa actin mRNAs are spatially restricted to the aboral ectoderm. Several DNA elements are localized at the same positions in the MTB1 and MTA genes: these include respective CATA and TATA boxes, two metal response elements, and three distinct upstream DNA elements that are also present, and in the same order, in the Spec 1 gene promoter. A heptameric sequence, element A, is present at two sites each in the Spec 1 and CyIIIa actin genes, five sites in MTA, but only one site in MTB1. Most strikingly, the first intron of MTA contains elements not found in the MTB1 introns, including a consensus metal response element, an element A, and the P3A site demonstrated in the CyIIIa actin gene to be linked to the regulation of spatial expression.
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Three metal complexing genes previously identified in sea urchins are metallothioneins MTA, MTB1, and MTB2.
“Three of the metal complexing genes found in the genome have previously been identified in sea urchins, the metallothioneins MTA, MTB1, and MTB2 (Nemer et al., 1991), which are active in response to excess metal stress but may also play roles in nutrient metal homeostasis and in apoptosis (reviewed in Vasak and Hasler, 2000).”
From The chemical defensome: Environmental sensing and response genes in the Strongylocentrotus purpuratus genome (2006) · cites this paper as Nemer et al., 1991
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References 54 · Cited by 51
- Authors
- Nemer, M., Thornton, R. D., Stuebing, E. W., & Harlow, P.
- Affiliations
- Fox Chase Cancer Center (US)
- Venue
- Journal of Biological Chemistry
- Publisher
- Elsevier BV
- Published
- 1991-04
- Volume
- 266
- Issue
- 10
- Pages
- 6586-6593
- ISSN
- 0021-9258 (ISSN-L)
- OpenAlex
- W1519893802
- Cited by
- 51
- References
- 54
- Citations by year
- 2019: 1 · 2016: 1 · 2013: 4 · 2012: 1
- FWCI
- 6.97
- Type
- journal article
- Language
- en
- Open access
- hybrid
- doi.org
- Licence
- Locations
- Journal of Biological Chemistry (publishedVersion, cc-by)
- PubMed (publishedVersion)
- Funders
- National Institutes of Health (2s07rr005539-29, 5r01hd004367-31)
- National Cancer Institute (P30CA006927, CA06927)
- National Center for Research Resources (RR-05539)
- Eunice Kennedy Shriver National Institute of Child Health and Human Development (HD-04367)
- Topics
- Health Sciences › Nursing › Nutrition and Dietetics › Trace Elements in Health
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Developmental Biology and Gene Regulation
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Genomics and Chromatin Dynamics
- Keywords
- metallothionein, Strongylocentrotus purpuratus, gene expression, spatial expressions, temporal expressions, metal response element, promoter elements, intron structure, embryonic development, blastula, mRNA localization, sea urchins
- MeSH terms
- Amino Acid Sequence, Animals, Base Sequence, DNA, Larva, Male, Metallothionein, Molecular Sequence Data, Nucleic Acid Hybridization, RNA, Messenger, Sea Urchins, Transcription, Genetic, Blotting, Southern, Gene Expression Regulation, Enzymologic, Polymerase Chain Reaction
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