High genetic variability of esterase loci in natural populations of Parus major, P. caeruleus, and P. ater.

Biochem Genet

Division of General Human Genetics, Institute of Anthropology and Human Genetics, University of Tübingen, Wilhelmstrasse 27, D-72074 Tübingen, Germany.

Published: April 2004

In Parus major, P. caeruleus, and P. ater the genetic variation of 16 isozyme loci was determined. The focus was on esterases that show high phenotypic variation in natural populations of these species. The degree of heterozygosity of the "non-esterase" loci was 0.029 +/- 0.008 (P. major); 0.023 +/- 0.012 (P. caeruleus), and 0.034 +/- 0.034 (P. ater). Including the esterase loci with up to six alleles per locus the overall degree of heterozygosity increased to 0.130 +/- 0.056 (P. major); 0.143 +/- 0.067 (P. caeruleus), and 0.194 +/- 0.090 (P. ater). We explain the high level of variability of esterases by gene amplification and subsequent selection for high allelic heterogeneity. Substrate specificity of loci is assumed to allow for multiple resistance against various toxic components. Large allelic valiation of esterases, therefore, increases the fitness of Parus species and allows for utilizing new food resources.

Download full-text PDF

Source
http://dx.doi.org/10.1023/b:bigi.0000020466.10868.dfDOI Listing

Publication Analysis

Top Keywords

esterase loci
8
natural populations
8
parus major
8
major caeruleus
8
caeruleus ater
8
degree heterozygosity
8
+/-
6
loci
5
high
4
high genetic
4

Similar Publications

The methylotrophic yeast belongs to the group of homothallic fungi that are able to spontaneously change their mating type by inversion of chromosomal DNA in the MAT locus region. As a result, natural and genetically engineered cultures of these yeasts typically contain a mixture of sexually dimorphic cells that are prone to self-diploidisation and spore formation accompanied by genetic rearrangements. These characteristics pose a significant challenge to the development of genetically stable producers for industrial use.

View Article and Find Full Text PDF

Coronary artery disease (CAD) is a multigenic condition influenced by both nature and nurture (60% to 40%). Prognosis of CAD is based on familial patterns. This study examined and analyzed the susceptibility of CAD to genetic variants in various Pakistani families.

View Article and Find Full Text PDF

Structural insights into how Cas9 targets nucleosomes.

Nat Commun

December 2024

Department of Biological Sciences, Graduate School of Science, The University of Tokyo, Tokyo, Japan.

The CRISPR-associated endonuclease Cas9 derived from prokaryotes is used as a genome editing, which targets specific genomic loci by single guide RNAs (sgRNAs). The eukaryotes, the target of genome editing, store their genome DNA in chromatin, in which the nucleosome is a basic unit. Despite previous structural analyses focusing on Cas9 cleaving free DNA, structural insights into Cas9 targeting of DNA within nucleosomes are limited, leading to uncertainties in understanding how Cas9 operates in the eukaryotic genome.

View Article and Find Full Text PDF

Phenotypic plasticity plays an essential role in adaptive evolution. However, the molecular mechanisms of how genotype-by-environment interaction (G × E) effects shape phenotypic plasticity in marine organisms remain poorly understood. The crucial temperature-responsive trait triacylglycerol (TAG) content and its major gene adipose triglyceride lipase (Atgl) expression have divergent plastic patterns in two congeneric oyster species (Crassostrea gigas and Crassostrea angulata) to adapt to relative-cold/northern and relative-warm/southern habitats, respectively.

View Article and Find Full Text PDF

Type 2 diabetes and the minor allele of PNPLA3 consistently identify high-risk metabolic dysfunction associated steatotic liver disease.

Diabetes Res Clin Pract

January 2025

The Global NASH Council, Washington, DC, United States; Beatty Liver and Obesity Research Program, Inova Health System, Falls Church, VA, United States; Center for Outcomes Research in Liver Diseases, Washington DC, United States.

Background: Association of genetic factors with non-invasive tests (NITs) for MASLD has not been well established.

Methods: Clinical and laboratory data, liver biopsy and/or liver stiffness measurement (LSM) by transient elastography were collected from MASLD patients seen in tertiary care hepatology practices. Minor allele frequency for genomic loci rs641738 (MBOAT7), rs58542926 (TM6SF2), rs738409 (PNPLA3), rs62305723 (HSD1713B) were evaluated for association with high ELF (≥11.

View Article and Find Full Text PDF

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!