Person:

Zhang, Liangran

Biological systems exhibit complex patterns, at length scales ranging from the molecular to the organismic. Along chromosomes, events often occur stochastically at different positions in different nuclei but nonetheless tend to be relatively evenly spaced. Examples include replication origin firings, formation of chromatin loops along chromosome axes and, during meiosis, designation of crossover recombination sites ("crossover interference"). We present evidence, in the fungus Sordaria macrospora, that crossover interference is part of a broader patterning program that includes synaptonemal complex (SC) nucleation. This program yields relatively evenly-spaced SC nucleation sites; among these, a subset is also crossover sites that show a classical interference distribution. This pattern ensures that SC forms regularly along the entire lengths of the chromosomes as required for homolog pairing maintenance and interlock sensing while concomitantly embedding crossover interactions within the SC structure as required for both DNA recombination and structural events of chiasma-formation. This pattern can be explained by a threshold-based interference process. This model can be generalized to give diverse types of related and/or partially overlapping patterns, in two or more dimensions, for any type of object.

Meiotic recombination initiates via programmed double-strand breaks (DSBs). We investigate whether, at a given initiation site, DSBs occur independently among the four available chromatids. For a single DSB “hot spot”, the proportions of nuclei exhibiting zero, one, or two (or more) observable events were defined by tetrad analysis and compared with those predicted by different DSB distribution scenarios. Wild-type patterns are incompatible with independent distribution of DSBs among the four chromatids. In most or all nuclei, DSBs occur one-per-pair of chromatids, presumptively sisters. In many nuclei, only one DSB occurs per four chromatids, confirming the existence of trans inhibition where a DSB on one chromosome interactively inhibits DSB formation on the partner chromosome. Several mutants exhibit only a one-per-pair constraint, a phenotype we propose to imply loss of trans inhibition. Signal transduction kinases Mec1 (ATR) and Tel1 (ATM) exhibit this phenotype and thus could be mediators of this effect. Spreading trans inhibition can explain even spacing of total recombinational interactions and implies that establishment of interhomolog interactions and DSB formation are homeostatic processes. The two types of constraints on DSB formation provide two different safeguards against recombination failure during meiosis.