Conservation of the heterochronic regulator Lin-28, its developmental expression and microRNA complementary sites
- PMID: 12798299
- DOI: 10.1016/s0012-1606(03)00126-x
Conservation of the heterochronic regulator Lin-28, its developmental expression and microRNA complementary sites
Erratum in
- Dev Biol. 2003 Oct 15;262(2):361
Abstract
The heterochronic gene lin-28 is a regulator of developmental timing in the nematode Caenorhabditis elegans. It must be expressed in the first larval stage and downregulated by the second stage for normal development. This downregulation is mediated in part by lin-4, a 21-nt microRNA. If downregulation fails due to a mutation in a short sequence in the lin-28 3' UTR that is complementary to lin-4, then a variety of somatic cell lineages fail to progress normally in development. Here, we report that Lin-28 homologues exist in diverse animals, including Drosophila, Xenopus, mouse, and human. These homologues are characterized by the LIN-28 protein's unusual pairing of RNA-binding motifs: a cold shock domain (CSD) and a pair of retroviral-type CCHC zinc knuckles. Conservation of LIN-28 proteins shows them to be distinct from the other conserved family of CSD-containing proteins of animals, the Y-box proteins. Importantly, the LIN-28 proteins of Drosophila, Xenopus, and mouse each appear to be expressed and downregulated during development, consistent with a conserved role for this regulator of developmental timing. In addition, the extremely long 3' UTRs of mouse and human Lin-28 genes show extensive regions of sequence identity that contain sites complementary to the mammalian homologues of C. elegans lin-4 and let-7 microRNAs, suggesting that microRNA regulation is a conserved feature of the Lin-28 gene in diverse animals.
Similar articles
-
Cloning and regulation of the vertebrate homologue of lin-41 that functions as a heterochronic gene in Caenorhabditis elegans.Dev Dyn. 2006 Apr;235(4):1142-9. doi: 10.1002/dvdy.20712. Dev Dyn. 2006. PMID: 16477647
-
acn-1, a C. elegans homologue of ACE, genetically interacts with the let-7 microRNA and other heterochronic genes.Cell Cycle. 2017 Oct 2;16(19):1800-1809. doi: 10.1080/15384101.2017.1344798. Epub 2017 Sep 21. Cell Cycle. 2017. PMID: 28933985 Free PMC article.
-
lin-28 controls the succession of cell fate choices via two distinct activities.PLoS Genet. 2012;8(3):e1002588. doi: 10.1371/journal.pgen.1002588. Epub 2012 Mar 22. PLoS Genet. 2012. PMID: 22457637 Free PMC article.
-
Control of developmental timing by small temporal RNAs: a paradigm for RNA-mediated regulation of gene expression.Bioessays. 2002 Feb;24(2):119-29. doi: 10.1002/bies.10046. Bioessays. 2002. PMID: 11835276 Review.
-
Control of developmental timing by micrornas and their targets.Annu Rev Cell Dev Biol. 2002;18:495-513. doi: 10.1146/annurev.cellbio.18.012502.105832. Epub 2002 Apr 2. Annu Rev Cell Dev Biol. 2002. PMID: 12142272 Review.
Cited by
-
Analysis on cDNA sequence, alternative splicing and polymorphisms associated with timing of puberty of Lin28B gene in goats.Mol Biol Rep. 2013 Aug;40(8):4675-83. doi: 10.1007/s11033-013-2562-y. Epub 2013 May 6. Mol Biol Rep. 2013. PMID: 23645087
-
Lin28 Regulates Cancer Cell Stemness for Tumour Progression.Cancers (Basel). 2022 Sep 24;14(19):4640. doi: 10.3390/cancers14194640. Cancers (Basel). 2022. PMID: 36230562 Free PMC article. Review.
-
LIN28B-mediated expression of fetal hemoglobin and production of fetal-like erythrocytes from adult human erythroblasts ex vivo.Blood. 2013 Aug 8;122(6):1034-41. doi: 10.1182/blood-2012-12-472308. Epub 2013 Jun 24. Blood. 2013. PMID: 23798711 Free PMC article.
-
miR-125b promotes early germ layer specification through Lin28/let-7d and preferential differentiation of mesoderm in human embryonic stem cells.PLoS One. 2012;7(4):e36121. doi: 10.1371/journal.pone.0036121. Epub 2012 Apr 24. PLoS One. 2012. PMID: 22545159 Free PMC article.
-
hnRNP Q/SYNCRIP interacts with LIN28B and modulates the LIN28B/let-7 axis in human hepatoma cells.PLoS One. 2024 Jul 8;19(7):e0304947. doi: 10.1371/journal.pone.0304947. eCollection 2024. PLoS One. 2024. PMID: 38976670 Free PMC article.
Publication types
MeSH terms
Substances
Grants and funding
LinkOut - more resources
Full Text Sources
Other Literature Sources
Molecular Biology Databases
Research Materials