Journal
CHROMOSOMA
Volume 130, Issue 4, Pages 251-262Publisher
SPRINGER
DOI: 10.1007/s00412-021-00764-x
Keywords
Satellite DNAs; Transposable elements; Repeatome; Stingless bees; Fluorescence in situ hybridization
Funding
- Conselho Nacional de Desenvolvimento Cientifico e Tecnologico-CNPq [308290/2020-8]
- FAPESP [2018/21772-5, 2020/06188-5]
- Fundacao de Amparo a Pesquisa do Estado de Sao Paulo (FAPESP) [2019/19069-7]
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Satellite DNAs and transposable elements are key components of constitutive heterochromatin in genomes. Through studying two species of Melipona bees with differing amounts of heterochromatin, significant differences in repeat landscape and amplification were observed, indicating quantitative and qualitative changes in evolution. The amplification of specific repeats, such as MscuSat01-195 and LTR/Gypsy_1, in Melipona scutellaris suggests their crucial role in c-heterochromatin evolution at the chromosomal level.
Satellite DNAs (satDNAs) and transposable elements (TEs) are among the main components of constitutive heterochromatin (c-heterochromatin) and are related to their functionality, dynamics, and evolution. A peculiar case regarding the quantity and distribution of c-heterochromatin is observed in the genus of bees, Melipona, with species having a low amount of heterochromatin and species with high amount occupying almost all chromosomes. By combining low-pass genome sequencing and chromosomal analysis, we characterized the satDNAs and TEs of Melipona quadrifasciata (low c-heterochromatin) and Melipona scutellaris (high low c-heterochromatin) to understand c-heterochromatin composition and evolution. We identified 15 satDNA families and 20 TEs for both species. Significant variations in the repeat landscapes were observed between the species. In M. quadrifasciata, the repetitive fraction corresponded to only 3.78% of the genome library studied, whereas in M. scutellaris, it represented 54.95%. Massive quantitative and qualitative changes contributed to the differential amplification of c-heterochromatin, mainly due to the amplification of exclusive repetitions in M. scutellaris, as the satDNA MscuSat01-195 and the TE LTR/Gypsy_1 that represent 38.20 and 14.4% of its genome, respectively. The amplification of these two repeats is evident at the chromosomal level, with observation of their occurrence on most c-heterochromatin. Moreover, we detected repeats shared between species, revealing that they experienced mainly quantitative variations and varied in the organization on chromosomes and evolutionary patterns. Together, our data allow the discussion of patterns of evolution of repetitive DNAs and c-heterochromatin that occurred in a short period of time, after separation of the Michmelia and Melipona subgenera.
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