PMID- 27541002 OWN - NLM STAT- MEDLINE DCOM- 20170523 LR - 20201215 IS - 1553-7404 (Electronic) IS - 1553-7390 (Print) IS - 1553-7390 (Linking) VI - 12 IP - 8 DP - 2016 Aug TI - Investigating the Interplay between Sister Chromatid Cohesion and Homolog Pairing in Drosophila Nuclei. PG - e1006169 LID - 10.1371/journal.pgen.1006169 [doi] LID - e1006169 AB - Following DNA replication, sister chromatids must stay connected for the remainder of the cell cycle in order to ensure accurate segregation in the subsequent cell division. This important function involves an evolutionarily conserved protein complex known as cohesin; any loss of cohesin causes premature sister chromatid separation in mitosis. Here, we examined the role of cohesin in sister chromatid cohesion prior to mitosis, using fluorescence in situ hybridization (FISH) to assay the alignment of sister chromatids in interphase Drosophila cells. Surprisingly, we found that sister chromatid cohesion can be maintained in G2 with little to no cohesin. This capacity to maintain cohesion is widespread in Drosophila, unlike in other systems where a reduced dependence on cohesin for sister chromatid segregation has been observed only at specific chromosomal regions, such as the rDNA locus in budding yeast. Additionally, we show that condensin II antagonizes the alignment of sister chromatids in interphase, supporting a model wherein cohesin and condensin II oppose each other's functions in the alignment of sister chromatids. Finally, because the maternal and paternal homologs are paired in the somatic cells of Drosophila, and because condensin II has been shown to antagonize this pairing, we consider the possibility that condensin II-regulated mechanisms for aligning homologous chromosomes may also contribute to sister chromatid cohesion. FAU - Senaratne, T Niroshini AU - Senaratne TN AD - Department of Genetics, Harvard Medical School, Boston, Massachusetts, United States of America. FAU - Joyce, Eric F AU - Joyce EF AD - Department of Genetics, Harvard Medical School, Boston, Massachusetts, United States of America. FAU - Nguyen, Son C AU - Nguyen SC AUID- ORCID: 0000-0003-2187-1027 AD - Department of Genetics, Harvard Medical School, Boston, Massachusetts, United States of America. FAU - Wu, C-Ting AU - Wu CT AD - Department of Genetics, Harvard Medical School, Boston, Massachusetts, United States of America. LA - eng GR - F32 CA157188/CA/NCI NIH HHS/United States GR - DP1 GM106412/GM/NIGMS NIH HHS/United States GR - RM1 HG008525/HG/NHGRI NIH HHS/United States GR - T32 GM096911/GM/NIGMS NIH HHS/United States GR - R01 GM085169/GM/NIGMS NIH HHS/United States PT - Journal Article PT - Research Support, N.I.H., Extramural DEP - 20160819 PL - United States TA - PLoS Genet JT - PLoS genetics JID - 101239074 RN - 0 (DNA-Binding Proteins) RN - 0 (Multiprotein Complexes) RN - 0 (condensin complexes) RN - EC 3.6.1.- (Adenosine Triphosphatases) SB - IM MH - Adenosine Triphosphatases/*genetics MH - Animals MH - Cell Nucleus/*genetics MH - Chromatids/genetics MH - Chromosome Segregation/genetics MH - Chromosomes/*genetics MH - DNA Replication/*genetics MH - DNA-Binding Proteins/*genetics MH - Drosophila melanogaster/genetics MH - In Situ Hybridization, Fluorescence MH - Metaphase/genetics MH - Mitosis/genetics MH - Multiprotein Complexes/*genetics MH - RNA Interference MH - Sister Chromatid Exchange/genetics PMC - PMC4991795 COIS- The authors have declared that no competing interests exist. EDAT- 2016/08/20 06:00 MHDA- 2017/05/24 06:00 PMCR- 2016/08/19 CRDT- 2016/08/20 06:00 PHST- 2016/01/28 00:00 [received] PHST- 2016/06/14 00:00 [accepted] PHST- 2016/08/20 06:00 [entrez] PHST- 2016/08/20 06:00 [pubmed] PHST- 2017/05/24 06:00 [medline] PHST- 2016/08/19 00:00 [pmc-release] AID - PGENETICS-D-16-00216 [pii] AID - 10.1371/journal.pgen.1006169 [doi] PST - epublish SO - PLoS Genet. 2016 Aug 19;12(8):e1006169. doi: 10.1371/journal.pgen.1006169. eCollection 2016 Aug.