Interactions between chromosomes and LINC (linker of nucleoskeleton and cytoskeleton) complexes in the nuclear envelope (NE) promote homolog pairing and synapsis during meiosis. By tethering chromosomes to cytoskeletal motors, these connections lead to rapid, processive movements of chromosomes along the NE. This activity is usually mediated by telomeres, but in the nematode C. elegans special chromosome regions called ″Pairing Centers″ (PCs) have acquired this meiotic function. Through a genetic screen for mutations causing meiotic nondisjunction in C. elegans, we discovered an uncharacterized meiosis-specific NE protein, MJL-1 (MAJIN-Like-1) that is essential for interactions between PCs and LINC complexes. MJL-1 colocalizes with PCs and LINC complexes during pairing and synapsis. Mutations in MJL-1 disrupt these interactions and eliminate active chromosome movements. Loss of mjl-1 mutants display promiscuous nonhomologous synapsis, reduced clustering of PCs, and severely impaired homolog pairing. Similarities in the molecular architecture of chromosome-LINC complex attachments between C. elegans and other organisms suggest that these connections may play previously unrecognized roles during meiosis across eukaryote.