Two two-gene macronuclear chromosomes of the hypotrichous ciliatesOxytricha fallax andO. trifallax generated by alternative processing of the 81 locus
- 1 January 1997
- journal article
- research article
- Published by Wiley in Developmental Genetics
- Vol. 20 (4) , 348-357
- https://doi.org/10.1002/(sici)1520-6408(1997)20:4<348::aid-dvg6>3.0.co;2-7
Abstract
We describe the first known macronuclear chromosomes that carry more than one gene in hypotrichous ciliated protozoa. These 4.9‐ and 2.8‐kbp chromosomes each consist almost exclusively of two protein‐coding genes, which are conserved and transcribed. The two chromosomes share a common region that consists of a gene that is a member of the family of mitochondrial solute carrier genes (CR‐MSC; [Williams and Herrick (1991): Nucleic Acids Res 19:4717–4724]. Each chromosome also carries another gene appended to its common region: The 4.9‐kbp chromosome also carries a gene that encodes a protein that is rich in glutamine and charged amino acids and bears regions of heptad repeats characteristic of coiled‐coils. Its function is unknown. The second gene of the 2.8 kbp chromosome is a mitochondrial solute carrier gene (LA‐MSC); thus, the 2.8‐kbp chromosome consists of two mitochondrial solute carrier paralogs. Phylogenetic analysis indicates that the two genes were duplicated before ciliates diverged from the main eukaryotic lineage and were subsequently juxtaposed. The CR‐ and LA‐MSC genes are each interrupted by three introns. The introns are not in homologous positions, suggesting that they may have originated from multiple group II intron transpositions. These chromosomes and their genes are encoded in the Oxytricha germline by the 81 locus. This locus is alternatively processed to generate a nested set of three macronuclear chromosomes, the 4.9‐ and 2.8‐kbp chromosomes and a third (1.6 kbp) which consists almost exclusively of the shared common gene, CR‐MSC. Such alternative processing is common in macronuclear development of O. fallax [Cartinhour and Herrick (1984): Mol Cell Biol 4:931–938]. Possible functions for alternative processing are considered; e.g., it may serve to physically link genes to allow co‐regulation or co‐replication by a common cis‐acting sequence. Dev. Genet. 20:348–357, 1997.Keywords
This publication has 49 references indexed in Scilit:
- Molecular evolution: A difficult phase for introns-earlyCurrent Biology, 1996
- Germline-soma relationships in ciliated protozoa: the inception and evolution of nuclear dimorphism in one-celled animalsSeminars in Developmental Biology, 1994
- Five identical intron positions in ancient duplicated genes of eubacterial originNature, 1994
- Programmed nuclear death: Apoptotic-like degradation of specific nuclei in conjugating TetrahymenaDevelopmental Biology, 1992
- Non‐Coding DNA in Macronuclear Chromosomes of Hypotrichous CiliatesThe Journal of Protozoology, 1992
- X-Ray Structure of the GCN4 Leucine Zipper, a Two-Stranded, Parallel Coiled CoilScience, 1991
- Predicting Coiled Coils from Protein SequencesScience, 1991
- Basic local alignment search toolJournal of Molecular Biology, 1990
- Multiple Sequence Versions of the Oxytricha fallax 81‐MAC Alternate Processing Family1The Journal of Protozoology, 1987
- Solute carriers involved in energy transfer of mitochondria form a homologous protein familyFEBS Letters, 1987