TABLE 5.
rec10 allele | Mutation | DSB proficient? | Crossover proficiency | Gene conversion proficiency | ade6–M26 hot spot proficiency | LinE status | Other |
---|---|---|---|---|---|---|---|
rec10-175a | Full open reading frame deletion | No | Noneb | Noneb | Noneb | Nonec | — |
rec10-109d | Two point mutationsa G526A (V176I) and G533A (G178D)e | Levels of DSBs diminishedf | Regionalgh | Regionalgh | Partialg | Abnormal LinEs formedci | Complements rec10-144jk. Slightly temperature sensitive for recombination at some regionsa |
rec10-144jk | Single point mutationj G2180A (G727E)e | Not determined | Limited reduction at all intervals testedl | Limited reduction at all intervals testedjl | Reduced hot spot activityj | Limited abnormal LinEs formedjm | Complements rec10-109jk |
rec10-155n | Insertion inactivation mutant; presumed C-terminal truncation of last 103 amino acidsn | Not determined | Limited reduction at all intervals testedl | Limited reduction at all intervals testedln | Reduced hot spot activityo | Noneimp | — |
Other rec10 mutant alleles have been isolated/generated and sequenced (De Veaux et al. 1992; Ellermeier and Smith 2005; our unpublished data), but they have undergone only limited analysis to date and are not listed here.
None equates to the levels observed for a rec12 null mutant.
As measured by immunocytochemistry.
Numbered from the start of the open reading frame.
Lorenz et al. (2004).
This study.
As determined by immunocytochemistry and electron microscopy.
D. W. Pryce and R. J. Mc Farlane (unpublished observation).