In summary, mutant analysis suggests that both exposed and non-exposed sensory neurons contribute to wild-type NH4Ac chemotaxis.
The mutant analysis suggests differential requirements for individual MCM proteins, however interpretation was complicated by the fact that individual MCM mutant lesions were of different types (MCM2rl74 is a P element insertion, dpa1, MCM6k1214 and MCM63 are point mutations).
Double mutant analysis suggests SVR3 and SVR7 act in different pathways in promoting chloroplast development.
Gene ontology analysis as well as stimulus responses and mutant analysis suggest that these proteins might in some instances function as antagonists of ABA, while inducing similar responses to those observed with cytokinin.
This gene mutant analysis suggests that the longer time required for ASEL neurons to reach their maximum response to odor may reflect the additional requirement of AWC-dependent peptidergic transmission.
In contrast, the overproduction or deletion of SSE1 cured the [ URE3] prion and mutant analysis suggests this activity is dependent on ATP binding and interaction with Hsp70 (Kryndushkin and Wickner 2007).
Double-mutant analysis suggested that AHO-3 acts in the same pathway with ODR-3, a heterotrimeric G protein alpha subunit.
Double-mutant analysis suggested that AHO-3 acts in the same pathway with ODR-3, a heterotrimeric G protein alpha subunit, which is localized to sensory endings (Roayaie et al. 1998; Bargmann 2006).
Mutant analysis has suggested the involvement of a MATE transporter for proanthocyanins in Arabidopsis [ 13], anthocyanins in tomato (Solanum lycopersicum, [ 14]) and maize (Zea mays, [ 15]).
Mutant properties and bioinformatic analysis suggested the reversion of K283R to improve stability, thus generating two additional mutants (K118/R159K and R118K/K232N/K241F/R283K).
We also calculated the energetic coupling between Asn123 β4) and Glu264 through molecular modeling and thermodynamic double-mutant cycle analysis, suggesting that Asn123 β4) might interact with Glu264.
