Search bioRxivSearch

Biology subjects

Lyu, Z.

Publications and source records attributed to Lyu, Z..

3 recordsLinked to original sources

Sense-antisense gene overlap causes evolutionary retention of the few introns in Giardia genome and the implications

BackgroundIt is widely accepted that the last eukaryotic common ancestor (LECA) and early eukaryotes were intron-rich and intron loss dominated subsequent evolution, thus the presence of only very few introns in some modern eukaryotes must be the consequence of massive loss. But it is striking that few eukaryotes were found to have completely lost introns. Despite extensive research, the causes of massive intron losses remain elusive, and actually the reverse question - how the few introns are retained under the pressure of loss is equally significant but was rarely studied, except that it was conjectured that the essential functions of some introns prevent their loss. The extremely few (eight) spliceosome-mediated cis-spliced introns in the relatively simple genome of Giardia lamblia provide an excellent opportunity to explore this question.\n\nResultsOur investigation of the intron-containing genes and introns in Giardia found three types of intron distribution patterns: ancient intron in ancient gene, relatively new intron in ancient gene, and relatively new intron in relatively new gene, which can reflect to some extent the dynamic evolution of introns in Giardia. Not finding any special features or functional importance of these introns responsible for the retention, we noticed and experimentally verified that some intron-containing genes form sense-antisense gene pairs with functional genes on their complementary strands, and that the introns just reside in the overlapping regions.\n\nConclusionsIn Giardias evolution, despite constant pressure of intron loss, intron gain can still occur in both ancient and newly-evolved genes, but only a few introns have been retained; the evolutionary retention of introns is most likely not due to the functional constraint of the introns themselves but the causes outside of introns, such as the constraints imposed by other genomic functional elements overlapping with the introns. These findings can not only provide some clues to find new genomic functional elements -- in the areas overlapping with introngs, but suggest that \"functional constraint\" of introns may not be necessarily directly associated with intron loss and gain, or that the real functions or the way of functioning of introns are probably still outside of our current knowledge.

genomics

Improved single-molecule localization precision in astigmatism-based 3D superresolution imaging using weighted likelihood estimation

Astigmatism-based superresolution microscopy is widely used to determine the position of individual fluorescent emitters in three-dimensions (3D) with subdiffraction-limited resolutions. This point spread function (PSF) engineering technique utilizes a cylindrical lens to modify the shape of the PSF and break its symmetry above and below the focal plane. The resulting asymmetric PSFs at different z-positions for single emitters are fit with an elliptical 2D-Gaussian function to extract the widths along two principle x- and y-axes, which are then compared with a pre-measured calibration function to determine its z-position. While conceptually simple and easy to implement, in practice, distorted PSFs due to an imperfect optical system often compromise the localization precision; and it is laborious to optimize a multi-purpose optical system. Here we present a methodology that is independent of obtaining a perfect PSF and enhances the localization precision along the z-axis. By utilizing multiple calibration images of fluorescent beads at varying z-planes and characterizing experimentally measured background distributions, we numerically approximated the probability of observing a certain signal in a given pixel from a single emitter at a particular z-plane. We then used a weighted maximum likelihood estimator (WLE) to determine the 3D-position of the emitter. We demonstrate that this approach enhances z-axis localization precision in all conditions we tested, in particular when the PSFs deviate from a standard 2D Gaussian model.

biophysics

Mmp10 is required for post-translational methylation of arginine at the active site of methyl-coenzyme M reductase

Catalyzing the key step for anaerobic methane production and oxidation, methyl-coenzyme M reductase or Mcr plays a key role in the global methane cycle. The McrA subunit possesses up to five post-translational modifications (PTM) at its active site. Bioinformatic analyses had previously suggested that methanogenesis marker protein 10 (Mmp10) could play an important role in methanogenesis. To examine its role, MMP1554, the gene encoding Mmp10 in Methanococcus maripaludis, was deleted with a new genetic tool, resulting in the specific loss of the 5-(S)-methylarginine PTM of residue 275 in the McrA subunit and a 40~60 % reduction in the maximal rates of methane formation by whole cells. Methylation was restored by complementations with the wild-type gene. However, the rates of methane formation of the complemented strains were not always restored to the wild type level. This study demonstrates the importance of Mmp10 and the methyl-Arg PTM on Mcr activity.

microbiology