The Bhalla lab isinterested in the mechanisms that ensure that chromosomes segregate correctly during cell division, particularly in meiosis. During this specialized cell division, diploid cells give rise to haploid gametes, such as sperm and eggs, so that diploidy is restored by fertilization. Defects in meiosis can generate gametes, and therefore embryos, with the incorrect number of chromsomes. These aberrations in chromosome number, also referred to as aneuploidy, typically produce inviable embryos. It is estimated that 30% of human miscarriages are due to aneuploidy. In some cases, the presence of an extra copy of a chromosome can be tolerated by a human embryo but results in serious developmental disorders, such as Down and Klinefelters syndrome.
Needhi Bhalla
Summary
Published articles Show More
HIM-8 binds to the X chromosome pairing center and mediates chromosome-specific meiotic synapsis.
Published in Cell
The him-8 gene is essential for proper meiotic segregation of the X chromosomes in C. elegans. Here we show that loss of him-8 function causes profound X chromosome-specific defects in homolog pairing and synapsis. him-8 encodes a C2H2 zinc-finger protein that is expressed during meiosis and concentrates at a site on the X chromosome known as the m...
ZHP-3 acts at crossovers to couple meiotic recombination with synaptonemal complex disassembly and bivalent formation in...
Published in PLoS Genetics
Crossover recombination and the formation of chiasmata normally ensure the proper segregation of homologous chromosomes during the first meiotic division. zhp-3, the Caenorhabditis elegans ortholog of the budding yeast ZIP3 gene, is required for crossover recombination. We show that ZHP-3 protein localization is highly dynamic. At a key transition ...
Chromosome sites play dual roles to establish homologous synapsis during meiosis in C. elegans.
Published in Cell
We have investigated the role of pairing centers (PCs), cis-acting sites required for accurate segregation of homologous chromosomes during meiosis in C. elegans. We find that these sites play two distinct roles that contribute to proper segregation. Chromosomes lacking PCs usually fail to synapse and also lack a synapsis-independent stabilization ...