Genomic exclusion and other micronuclear anomalies are common in genetically defective clones of tetrahymena thermophila.
نویسندگان
چکیده
Genomic exclusion (GE) is an abnormal form of conjugation which has previously been described in detail for three hypodiploid strains of Tetrahymena thermophila. These strains cannot form gametic nuclei and by failing to participate in normal reciprocal fertilization their genes are excluded from exconjugants. To determine whether GE is a general property of infertile strains, we surveyed genetically and cytogenetically 19 additional strains of T. thermophila to determine why they failed to contribute genes to sexual progeny. Crosses to genetically marked tester strains showed that seventeen of these strains undergo GE. In each case GE appears to be due to the failure of the defective partner to form functional gametic nuclei. The normal conjugant, however, contributes to its defective partner a haploid nucleus identical to its own, and following diploidization of the unfertilized nuclei, the conjugants separate retaining the old macronuclei. Cytofluorimetric measurement of micronuclear DNA content in 18 strains suggests that aneuploidy is the proximate cause of GE; eleven strains were hypodiploid, five were diploid and three were hyperdiploid. Many irregular cytogenetic events were observed in conjugants presumably not undergoing GE, including, in some instances, abnormal meiosis in the normal partner. Since genomic exclusion was found in both wildtype and mutant clones, the results suggest that it should be possible by appropriate crosses to identify genomic exclusion strains of any genotype.
منابع مشابه
Tetrahymena macronuclear genome mapping: colinearity Of macronuclear coassortment groups and the micronuclear map on chromosome 1l.
The genetics of the ciliate Tetrahymena thermophila are richer than for most other eukaryotic cells, because Tetrahymena possesses two genomes: a germline (micronuclear) genome that follows a Mendelian model of genetic transmission and a somatic (macronuclear) genome, derived from the micronuclear genome by fragmentation, which follows a different genetic transmission model called phenotypic as...
متن کاملMicronucleus-specific histone H1 is required for micronuclear chromosome integrity in Tetrahymena thermophila
Histone H1 molecules play a key role in establishing and maintaining higher order chromatin structures. They can bind to linker DNA entering and exiting the nucleosome and regulate transcriptional activity. Tetrahymena thermophila has two histone H1, namely, macronuclear histone H1 and micronuclear histone H1 (Mlh1). Mlh1 is specifically localized at micronuclei during growth and starvation sta...
متن کاملGerm line-specific DNA sequences are present on all five micronuclear chromosomes in Tetrahymena thermophila.
The development of the macronucleus from the zygotic micronucleus in the ciliated protozoan Tetrahymena spp. involves the elimination of specific DNA sequences (M. C. Yao and M. Gorovsky, Chromosoma 48:1-18 1974). The present study demonstrates that micronucleus-specific DNA is present on all five of the micronuclear chromosomes. Fragments of micronuclear DNA from Tetrahymena thermophila were c...
متن کاملThe regulation of amounts and proportions of genetic elements in the macronuclei of Tetrahymena thermophila strains of diverse karyotype.
Measurements of the micronuclear DNA content of clones with assumed different degrees of micronuclear ploidy confirmed the triploid nature of one clone. The micronuclear DNA content of a presumptive haploid clone was found to be slightly higher than expected, whereas one of two aneuploid clones had an unexpectedly low micronuclear DNA content. The macronuclear DNA content of cells with macronuc...
متن کاملThe transition from conjugal development to the first vegetative cell division is dependent on RAD51 expression in the ciliate Tetrahymena thermophila.
Rad51p, the eukaryotic homolog of the prokaryotic recA protein, catalyzes strand exchange between single- and double-stranded DNA and is involved in both genetic recombination and double-strand break repair in the ciliate Tetrahymena thermophila. We have previously shown that disruption of the Tetrahymena RAD51 somatic macronuclear locus leads to defective germline micronuclear division and tha...
متن کاملذخیره در منابع من
با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید
عنوان ژورنال:
- Genetics
دوره 120 1 شماره
صفحات -
تاریخ انتشار 1988