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Open AccessJournal ArticleDOI

Conditional-lethal mutations that suppress genetic defects in morphogenesis by altering structural proteins.

Jonathan Jarvik, +1 more
- 01 Jul 1975 - 
- Vol. 72, Iss: 7, pp 2738-2742
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TLDR
It is shown that genetic reversion of missense mutants can be of value in producing new temperature-sensitive and cold-sensitive mutations affecting related functions and it is suggested that the approach can be extended to organisms with large genomes.
Abstract
An analysis of revertants of missense mutants in phage P22 has shown: (i) New temperature-sensitive (TS) and cold-sensitive (CS) phenotypes are often acquired concomitant with reversion. (ii) In many cases, these new phenotypes are due to second-site mutations (suppressors) that correct the original defect. (iii) Sometimes the suppressor mutation is not in the same gene as the original mutation. (iv) Extragenic suppressors are almost always in genes whose products are known to interact physically with the original gene products. (v) The suppressor mutations typically retain their TS or CS phenotypes when crossed into wild-type genetic backgrounds. (vi) Some TS and CS mutants derived by reversion can themselves be reverted to produce additional mutations. We have shown that genetic reversion of missense mutants can be of value in producing new temperature-sensitive and cold-sensitive mutations affecting related functions. We suggest that our approach can be extended to organisms with large genomes.

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MCM Proteins in DNA Replication

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Mapping T-cell receptor-peptide contacts by variant peptide immunization of single-chain transgenics.

TL;DR: Charge substitutions on the peptide often elicit reciprocal charges in the junctional sequences of T-cell receptor Vαor Vβ chains, indicating direct T- Cell receptor–peptide contact, and allowing derivation of a topology for the T- cell receptor–MHC interaction.
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Isolation of genes by complementation in yeast: molecular cloning of a cell-cycle gene.

TL;DR: Recombinant plasmids capable of complementing cdc28 mutations were isolated by transformation of a cDC28ts strain and selection for clones capable of growth at the restrictive temperature, confirming the identity of the cloned sequences.
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