4.8 Article

Formation of the CenH3-Deficient Holocentromere in Lepidoptera Avoids Active Chromatin

Journal

CURRENT BIOLOGY
Volume 31, Issue 1, Pages 173-+

Publisher

CELL PRESS
DOI: 10.1016/j.cub.2020.09.078

Keywords

-

Funding

  1. Labex DEEP, IDEX Idex PSL [ANR-11-LABX-0044, ANR-10-IDEX-0001-02 PSL]
  2. ATIP-AVENIR Research grant
  3. ERC [CENEVO-758757]
  4. JSPS KAKENHI [15H02482]
  5. Grants-in-Aid for Scientific Research [15H02482] Funding Source: KAKEN

Ask authors/readers for more resources

This study provides a chromatin-level description of CenH3-deficient holocentromeres in the silk moth Bombyx mori, revealing a correlation between centromere sites and regions of low chromatin activity. Transcriptional perturbation experiments confirm the exclusion of centromeres from active chromatin in B. mori.
Despite the essentiality for faithful chromosome segregation, centromere architectures are diverse among eukaryotes(1,2) and embody two main configurations: mono- and holocentromeres, referring, respectively, to localized or unrestricted distribution of centromeric activity. Of the two, some holocentromeres offer the curious condition of having arisen independently in multiple insects, most of which have lost the otherwise essential centromere-specifying factor CenH3(3) (first described as CENP-A in humans).(4-7) The loss of CenH3 raises intuitive questions about how holocentromeres are organized and regulated in CenH3-lacking insects. Here, we report the first chromatin-level description of CenH3-deficient holocentromeres by leveraging recently identified centromere components 6 ' 7 and genomics approaches to map and characterize the holocentromeres of the silk moth Bombyx mori, a representative lepidopteran insect lacking CenH3. This uncovered a robust correlation between the distribution of centromere sites and regions of low chromatin activity along B. mori chromosomes. Transcriptional perturbation experiments recapitulated the exclusion of B. mori centromeres from active chromatin. Based on reciprocal centromere occupancy patterns observed along differentially expressed orthologous genes of Lepidoptera, we further found that holocentromere formation in a manner that is recessive to chromatin dynamics is evolutionarily conserved. Our results help us discuss the plasticity of centromeres in the context of a role for the chromosome-wide chromatin landscape in conferring centromere identity rather than the presence of CenH3. Given the co-occurrence of CenH3 loss and holocentricity in insects,(7) we further propose that the evolutionary establishment of holocentromeres in insects was facilitated through the loss of a CenH3-specified centromere.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.8
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available