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The yellow-throated marten (Martes flavigula) is a flamboyant oddball in the genus Martes, which also includes the sable, pine marten, stone marten, Japanese marten, and American martens. Unlike any other marten species, yellow-throated martens hunt in packs, usually made up of siblings, and are frighteningly good at that: they successfully take down much bigger animals, such as water deer and macaques. In fact, they appear to be much more advanced socially than their loner relatives – while the overall color of their coat is an olive-tinged agouti-to-black gradient, providing good camouflage in lush foliage, some markings almost definitely serve the purpose of biocommunication: the contrasting black head and white chin, bright yellow chest, and long, black tail are amazingly similar to patterns seen in highly social simians, such as squirrel monkeys.

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Martes flavigula, yellow-throated marten by Rushen, [CC BY-SA 2.0], via flickr.com

As of now, the yellow-throated marten is listed as LC (Least Concern) by the IUCN due to wide distribution and considerable numbers, as well as its presence in a number of protected territories. However, like most other martens, it prefers large continuous stretches of old-growth primeval forests, and uncontrolled logging and consequent habitat fragmentation and loss are causing an ongoing decline of its numbers in some parts of its range, which stretches from Pakistan in the west to the Russian Far East in the east and the island of Borneo in the south. In the Russian Far East, the yellow throated-marten, locally known as kharza, coexists with another member of the genus - the sable (Martes zibellina), albeit not always peacefully.


The unusual for martens combination of morphological, genetic and behavioral differences has led some researchers to believe that Martes flavigula, together with its sister species, the Nilgiri marten (Martes gwatkinsii) should be assigned a genus of their own. Further genomic research will help to assess whether this suggestion is founded. Moreover, the species as a whole is poorly studied, and there are reasons to believe that some of the isolated patches that make up its range may in fact host distinct subspecies or even separated species.


Today, we present the chromosome-length assembly for the third marten species of this year. All C-scaffolds of the yellow-throated marten were assigned to the corresponding chromosomes via a Zoo-FISH experiment with the stone marten chromosomes used as probes. In contrast to other marten species, Martes flavigula have more chromosomes: 2n=40 instead of 2n=38. (Fig. 1): you can see the chromosome corresponding to chr8 in the stone marten into two chromosomes (chr9 and 19) in the yellow-throated marten in the whole-genome alignment plot below!

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Figure 1. Dotplot for whole genome alignment of yellow-throated marten genome to stone marten assembly

We thank Dr. Rogell Powell (North Carolina State University) for funding 10x Genomics linked-read sequencing for the draft assembly and Dr. Klaus Koepfli and Dr. Alexander Graphodatsky for organizing this sequencing and bringing all of the collaborators together. Also we thank Olga Shilo (deputee director), Rosa Solovyova (head of carnivore department) and Svetlana Verkholantseva (veterinarian) from Rostislav Shilo Novosibirsk Zoo (Russia, Novosibirsk) who provided samples for a cell line. Samples were collected postmortem from a 15-year old male individual called Dixi. These cells were used for both DNA extraction for linked read sequencing and for the Hi-C experiment. DNA extraction and Zoo-FISH experiments were performed by Natalia Serdyukova and Dr Violetta Beklemisheva. The initial assembly was performed by Sergei Kliver. Hi-C experiments and scaffolding to chromosomes were done by Dr. Polina Perelman, Ruqayya Khan and Dr. Olga Dudchenko. The genome annotation and a paper describing this research is in progress.


 
 
 

DNA Zoo Novosibirsk at the Institute of Molecular and Cellular Biology (Siberian Branch of Russian Academy of Sciences) joined the team of DNA-Zoo on August 25, 2020. The team is situated at the scientific hub - Academgorodok, Novosibirsk in the beautiful part of Russia - Southern Siberia.

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Dr. Alexander Graphodatsky is a head of the team and the Department of Genomic Diversity at the Institute (https://www.mcb.nsc.ru/laboratory/lca; https://www.mcb.nsc.ru/laboratory/lcg). Dr. Graphodasky is a cytogeneticist who was at the forefront of comparative research of animal and human chromosomes by karyology, chromosome painting, and genomics in Russia. Dr. Graphodatsky’s leadership led to a gathering of our productive multidisciplinary team.

Chromosomal sets of animal species have a different number of chromosomes (2n or diploid number). Humans have 2n=46, the Indian muntjac has 2n=6, and the viscacha rat has 2n=102. Yet, we, mammals, all share almost the same genetic material. Why such a great difference in the number of chromosomes? We know from the research that changes in karyotypes during the evolution of mammals manifest in genome reshuffling events through fusions, fissions, inversions, and heterochromatin expansion of ancestral chromosomal elements leading to drastic changes in species diploid numbers. Still, underlying mechanisms and reasons for major genomic reshuffling are largely unknown.


DNA Zoo Novosibirsk will be using an extensive collection of fibroblast cell lines and frozen tissues of animals from across Europe and Asia as well as of World fauna assembled by the members of the team through the years. It is the largest collection of animal cell lines in Russia (https://www.mcb.nsc.ru/node/866)!


The diverse team of DNA-Zoo Novosibirsk includes cytogeneticists, molecular biologists, bioinformaticians, and ancient DNA geneticists. DNA-Zoo Novosibirsk collaborates with Zoos and reserves.


Our goal at DNA-Zoo is to assemble genomes of the fauna of Russia and neighboring countries to the chromosome level and to uncover underlying mechanisms of the genomic changes leading to the formation of our own human genome.


To mark the launch of DNA Zoo Novosibirsk, we have recently released the genome assemblies for the stone marten and the beech marten. Please check them out if you have not already! We follow up today with more genome assemblies based on the DNA Zoo Novosibirsk collection, the yellow-throated marten and the jaguarundi. Stay tuned for more!

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Cytogenetics and Molecular Genetics


Alexander Graphodatsky

Vladimir Trifonov

Svetlana Romanenko

Polina Perelman

Violetta Beklemisheva

Natalya Serdyukova

Anastasiya Proskuryakova

Larisa Biltueva

Natalya Lemskaya

Guzel Davletshina

Maria Pobedintseva

Daria Andreyushkova

Ekaterina Tishakova


Zoology

Tatyana Bulionkova


Bioinformatics

Sergey Kliver

Dmitry Prokopov

Aleksey Makunin

Iliya Kichgin

Mikhail Fofanov


Ancient DNA

Nadejda Vorobieva

Anna Druzhkova

Maria Kusliy

Yulia Fedorova


Metagenomics

Anastasiya Kulemsina


The Soul of the Team

Yuliya Butakova


 
 
 

Stony coral are a major keystone species for coral reef ecosystems. Although coral reefs cover 1% of the ocean floor, they are home to more than 25% of the ocean’s known biodiversity and provide habitat for many marine organisms [1].


Unfortunately, coral reefs are in decline in the U.S. and around the world. Increased ocean temperatures and changing ocean chemistry are the greatest global threats to coral reef ecosystems. These threats are caused by warmer atmospheric temperatures and increasing levels of carbon dioxide in seawater. Ecological stress brought on by changes in temperature, salinity, or acidification levels can break down the symbiotic relationship between reef-building coral and their intracellular photosynthetic dinoflagellates in a phenomenon known as bleaching [2].

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Acropora millepora in the Great Barrier Reef by Petra Lundgren, Juan C Vera, Lesa Peplow, Stephanie Manel and Madeleine JH van Oppen, [CC BY 4.0], via wikimedia.org

Today, we highlight a chromosome-length genome assembly from our recent manuscript, for the species Acropora millepora, a scleractinian coral that inhabits coral reefs across the planet’s shallow ocean water. This chromosome-length assembly was generated via a Hi-C upgrade (using 3D-DNA and Juicer, see our Methods page for more details) of a draft genome assembly from (Ying et al., 2019). The A. millepora tissue used to generate the Hi-C data for the upgrade was obtained from a healthy coral identified by its skeletal morphology, particularly the arrangement of peripheral and axial coralites[DC1] . The sample was taken from a mature adult A. millepora that has established itself as a colony with a calcium carbonate skeleton.


To our knowledge, this is the first three-dimensional 3D-genome assembly of the A. millepora genome, and the first stony coral to have its genome three dimensionally mapped. A recently published excellent independent effort focusing on Genome Wide Association Studies (GWAS) of bleaching across 253 different coral larvae relied on a linkage map-based chromosome-level genome assembly [2]. We hope that Hi-C data will not only help with improving the chromosome-length assembly for A. millepora and the associated downstream analyses, but also contribute to our understanding of the complex regulatory landscape associated with the complex phenomenon of bleaching, e.g., shed some light on the 3D arrangement of the locus encoding transcription of the heat-shock co-chaperone sacsin.

 
 
 

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