Tag Archives: Plant Genomes

The Draft Genome Of Watermelon: Citrullus lanatus

The Cucurbitaceae is an agriculturally important family of plants (think melons, pumpkins, cucumbers, squashes, etc.) and one of the most popular species in this family is Watermelon.  Watermelon has been cultivated for more than 4,000 years and was most probably spread by nomadic people as a portable source of both water and pre-packaged nutrients.  The estimated center of diversity of the Cucurbits is in Southern Africa.  Watermelon has many cultivars – more than 200 in production worldwide – with a wide range of phenotypic diversity and a wide area of production that accounts for 7% of land grown for vegetables.


Unfortunately, Curcubits are generally susceptible to pathogens – most typically in the form of bacterial and fungal pathogens.  The genomes in this group are starting to pile up which makes the family an interesting group for comparative genomics studies –particularly in the development of model species for plant pathogen studies.

watermelon genome paper header

The recently published paper “The draft genome of watermelon (Citrullus lanatus) and resequencing of 20 diverse accessions” by Guo et al. in the journal Nature Genetics, described the draft genome for the Citrullus lanatus East Asian cultivar 97103 and then re-sequenced 20 different watermelon accessions – representing three different sub-species – in order to observe genetic diversity in wild.

Almost 47 Gb of sequence data was generated using Illumina’s sequencing platforms to give 108X coverage on the relatively small estimation of 426 Mb C. lanatus genome, while the draft is approximately 353 Mb or 83.2% of the estimated genome size.  Unmapped reads, totaling almost 20% of the sequencing data, could not accurately be constructed into contigs because of explicit regions of genome duplication.

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The authors estimated 23,440 genes in the watermelon genome – very close to both the cucumber genome (no surprise) and the human genome (surprise).  About 85% of the genes from watermelon could be predicted on the basis of homology to other plant genes.  The authors did a throughout assessment of transposable elements, various repeats, and classified functional RNAs from ribosomal RNA subunits to microRNAs.  Like other plants, watermelon shows gene enrichment in subtelomeric regions.  On the basis of comparison to other genome sequences, watermelon possesses the seven paleotriplications shared with the eudicots.

watermelon paper figure 2

The authors assessed genetic diversity across varieties of C. lanatus by sequencing 20 representative accessions anywhere between 5X and 16X coverage.  The estimated diversity of these accessions was considerably lower than similar arrays of accessions in maize, soybean, and rice.  One explanation of the disease susceptibility of the Cucurbitaceae is this low level of genetic diversity.  As a result, one objective of breeding programs for watermelon is to introduce more diversity from wild accessions.

watermelon paper figure 3

Lastly, the authors assessed a number of key features of the C. lanatus genome (along with the other Cucurbitaceae): vascular transport of water and nutrients along vine-like stems, sugar content and accumulation, and the presence of an interesting non-essential amino acid – originally described from watermelons – called Citrulline.

The watermelon genome database is located both here and here.

A Genome Sequence for Tomato

The average person in the United States eats more than 10 kilograms of tomatoes a year – underscoring the fact that the fruit is one of the most important plant crops in cultivation.  To improve taste, texture, and disease resistance – just to name a few traits – a large consortium of researchers has initiated and provided a draft tomato genome.  In fact, the research consortium has published the genome sequence from two varieties of tomatoes: the domesticated inbred Solanum lycopersicum strain Heinz 1706 – the variety famous for ketchup – and the wild breeding Peruvian ancestor, Solanum pimpinellifolium.

The consortium published the draft genome sequences with a paper entitled “The tomato genome sequence provides insights into fleshy fruit evolution” in the journal Nature.  The consortium started sequencing the genome officially in 2003, but heterozygosity and duplication events made assembling the genome difficult.  The tomato genome is approximately 900 Mb – smaller than the Human genome – but certainly not small by eukaryotic standards.  Genetically and phenotypically diverse, the genus Solanum is one of the largest in the angiosperms.

The genomes of Solanum lycopersicum and S. pimpinellifolium only show 0.6% divergence and there is evidence of recent hybridization between the two species.  Both species show approximately 8% genome divergence compared against close relative potato, Solanum tuberosum.  Across the genus Solanum there has been two genome triplications with subsequent gene loss: one genome triplication is ancient and shared with all the rosid clade and another triplication is shared within the Solanaceae, which appear to be highly syntenic across the family.  The genomes were completed with both Sanger- and Illumina-derived sequences and assembled with the help of physical and genetic maps developed from a long history of tomato breeding efforts.

There are 34,727 and 35,004 genes identified across the genomes of Solanum lycopersicum and S. pimpinellifolium respectively.  These findings are similar to other plant genomes as 8,615 of these genes are found to be common to tomato, potato, rice, grape, and Arabidopsis.  Expression was assessed by replicated RNA-Seq of root, leaf, flower, and fruit tissues.  A total of 18,320 orthologous gene pairs were found in tomato and potato indicating diversifying selection between the two species of Solanum.

The consortium specifically compared tomato to grape in this study, as grape and tomato shared a common ancestor at approximately 100 million years ago, before the first whole genome triplication event that preceded the rosid-asterid divergence.  Additionally, both grape and tomato have similar molecular fruit maturation mechanisms.  When comparing the genomes of tomato and grape, approximately 73% of gene models are orthologous.  By estimating genome triplication events, the researchers conclude that the genome duplication event within the Solanaceae occurred roughly 71 million years ago and approximately 7 million years prior to the tomato-potato divergence.

Having a draft genome sequence is an important mechanism to understanding the molecular biology of the tomato plant.  Genome duplication events gave rise to the diversification of genes responsible for enhanced fruit physiological and chemical development – such as lycopene synthesis – and include photoreceptors and transcription factors that influence fruit ripening.  Additionally, tomato has had a contraction in the number of gene families associated with toxic alkaloid synthesis – the chemical hallmarks of many members of the Solanaceae.  One interesting question not answered by this research is the genomic mechanism by which the tomato regulates nutrient investment in above-ground fruits while the potato regulates starch investment in below-ground tubers.

These two tomato genomes, along with the genomes of fellow Nightshades completed or in the works (potato, pepper, tobacco, petunia, eggplant, etc.), will help breeders to develop traits desired by producers, like long shelf life, and fruit quality traits desired by tomato-consumers, such as taste, color, and texture.  In addition to these benefits, the draft tomato genomes will provide insights into the biology and nutrition of the Solanaceous plants, and provide more information for comparative genomics within this important economic group of plants.

The Medicago Genome Provides Insight Into the Evolution of Rhizobial Symbioses

Legumes are a very successful lineage of plants which have developed associations with soil microbes, most notably endosymbiotic nitrogen fixing bacteria.  Nitrogen fixation is found in specialized plant root structures called nodules.  Published online on November 16th in the journal Nature was the article “The Medicago genome provides insight into the evolution of rhizobial symbioses” by Young et al. (Another paper concerning the Medicago genome recently appeared in the journal PNAS).  Medicago truncatula, the plant sequenced in this paper, is related to the economically important crop alfalfa (Medicago sativa) and is a commonly used model plant to study above and below ground plant biology, most notably interactions with symbiotic microorganisms.

The Medicago genome (like most genomes) is still in the draft stage.  Through the use of bacterial artificial chromosomes (BACs) and direct sequencing of genomic DNA, the researchers estimate the genome of Medicago is upwards of 350 Mb in length.  As an estimation of the completeness of the M. truncatula genome, approximately 94% of expressed genes (as ESTs) map to the draft genome.  An estimated number of genes for M. truncatula is 62,388, with an average gene size of 2,211 base pairs per gene, and an average of 4 exons per gene.  These numbers seem to be in the same “ballpark”, or perhaps larger, than the genomes of Poplar, Rice, and Arabidopsis.

The sequencing of numerous plant genomes, including M. truncatula here, indicates a whole genome duplication event which occurred prior to the split of the rosids from the asteroids at approximately 150 million years ago.  Another whole genome duplication event occurred at approximately 60 million years ago in the Legumes, which yielded several subclades, with Medicago being placed in the Hologalegina clade.

Significant synteny is shared between Medicago and the genomes of other sequenced legumes, Glycine max and Lotus japonicus.  A common ancestor of the legumes underwent a whole genome duplication event, occurring approximately 58 million years ago, and as a result, specific euchromatic regions of Medicago share synteny with numerous regions in each of the Lotus and Glycine genomes, as well as other regions of the Medicago genome.  Additionally, due to a pre-Rosid whole genome duplication event, the genome of Medicago shows synteny to the grape genome in at least three elongated regions.

There has been a high rate of local gene duplication events – some by tandem duplication – in the Medicago genome, and these events are approximately three fold higher than Glycine and one and a half times greater than both Populus and Arabidopsis.  Gene duplication events in Medicago could explain the average to above average number of genes observed in the genome.  Based on the estimated time of origin for the legumes, Medicago has undergone synonymous substitutions at a rate almost twice that of the average rate of vascular plants.

Production of a specialized organ, the root nodule, in many members of the legumes is a trait with both ecological importance and human agricultural interest.  Through the structure of the root nodule, leguminous plants harbor anaerobic actinorhizal bacteria which are capable of fixing atmospheric nitrogen.  It appears that the trait of nodulation has evolved numerous times in the Fabales, and was reliant on whole genome duplication events which allowed the emergence of novel gene functions from redundant genes.

There are numerous plant genomic features present in the Legumes with regard to signaling with rhizobial microorganisms, such as nitrogen fixing bacteria and mycorrhizal fungi.  Duplicated genes have evolved roles in nodulation formation (the genes NFP and ERN1) and mycorrhizal colonization (the genes LYR1 and ERN2).  The researchers used RNA-Seq data from six different plant organs to differentiate gene expression of putative whole genome duplicated paralogs.  Not surprisingly for Medicago, roots had the highest amount of differential expression of paralogous genes, followed by flower, nodule, leaf, seed, and flower bud.  Transcription factors, putatively responsible for tissue differentiation in gene expression, were estimated to be 6% of all Medicago genes.

One Hundred Important Questions Facing Plant Science Research

The October issue of the journal New Phytologist contains a commentary article by a group of plant scientists who conducted a survey to identify the 100 most pressing scientific questions facing plant biologists.  The article “One Hundred Important Questions Facing Plant Science Research” is very thought provoking.

I’ve replicated the questions here for you to read and ponder.  I know the list is heavy on the text, but I think these questions are worthy of the space.  You should definitely then read their article (and supplementary commentary) and see how they have collectively addressed these questions.  They may have addressed these questions in their commentary, but these questions are far from answered and may demand many careers to answer fully.

 Most important questions relating to plants and society:

1. How do we feed our children’s children?

2. Which crops must be grown and which sacrificed, to feed the billions?

3. When and how can we simultaneously deliver increased yields and reduce the environmental impact of agriculture?

4. What are the best ways to control invasive species including plants, pests and pathogens?

5. Considering two plants obtained for the same trait, one by genetic modification and one by traditional plant breeding techniques, are there differences between those two plants that justify special regulation?

6. How can plants contribute to solving the energy crisis and ameliorating global warming?

7. How do plants contribute to the ecosystem services upon which humanity depends?

8. What new scientific approaches will be central to plant biology in the 21st Century?

9. (a) How do we ensure that society appreciates the full importance of plants? (b) How can we attract the best young minds to plant science so that they can address Grand Challenges facing humanity such as climate change, food security, and fossil fuel replacement?

10. How do we ensure that sound science informs policy decisions?

11. How can we translate our knowledge of plant science into food security?

12. Which plants have the greatest potential for use as biofuels with the least effects on biodiversity, carbon footprints and food security?

13. Can crop production move away from being dependent on oil-based technologies?

14. How can we use plant science to prevent malnutrition?

15. How can we use knowledge of plants and their properties to improve human health?

16. How do plants and plant communities (morphology, color, fragrance, sound, taste etc.) affect human well-being?

17. How can we use plants and plant science to improve the urban environment?

18. How do we encourage and enable the interdisciplinarity that is necessary to achieve the UN’s Millennium Development Goals which address poverty and the environment?

 Most important questions relating to environment and adaptation:

1. How can we test if a trait is adaptive?

2. What is the role of epigenetic processes in modulating response to the environment during the life span of an individual?

3. Are there untapped potential benefits to developing perennial forms of currently annual crops?

4. Can we generate a step-change in C3crop yield through incorporation of a C4 or intermediate C3/C4 or crassulacean acid metabolism (CAM) mechanism?

5. How do plants regulate the proportions of storage reserves laid down in various plant parts?

6. What is the theoretical limit of productivity of crops and what are the major factors preventing this being realized?

7. What determines seed longevity and dormancy?

8. How can we control flowering time?

9. How do signaling and cross-talk between the different plant hormones operate?

10. Can we develop salt/heavy metal/drought-tolerant crops without creating invasive plants?

11. Can plants be better utilized for large-scale remediation and reclamation efforts on degraded and/or toxic land?

12. How can we translate our knowledge of plants and ecosystems into ‘clever farming’ practices?

13. Can alternatives to monoculture be found without compromising yields?

14. Can plants be bred to overcome dry land salinity or even reverse it?

15. Can we develop crops that are more resilient to climate fluctuation without yield loss?

16. Can we understand (explain and predict) the succession of plant species in any habitat, and crop varieties in any location, under climate change?

17. To what extent are the stress responses of cultivated plants appropriate for current and future environments?

18. Are endogenous plant adaption mechanisms enough to keep up with the pace of man-made environmental change?

19. How can we improve our cultivated plants to make better use of finite resources?

20. How do we grow plants in marginal environments without encouraging invasiveness?

21. How can we use the growing of crops to limit deserts spreading?

 Most important questions relating to plant species interactions:

1. What are the best ways to control invasive species including plants, pests and pathogens?

2. Can we provide a solution to intractable plant pest problems in order to meet increasingly stringent pesticide restrictions?

3. Is it desirable to eliminate all pests and diseases in cultivated plants?

4. What is the most sustainable way to control weeds?

5. How can we simultaneously eradicate hunger and conserve biodiversity?

6. How can we move nitrogen-fixing symbioses into non-legumes?

7. Why is symbiotic nitrogen fixation restricted to relatively few plant species?

8. How can the association of plants and mycorrhizal fungi be improved or extended towards better plant and ecosystem health?

9. How do plants communicate with each other?

10. How can we use our knowledge of the molecular biology of disease resistance to develop novel approaches to disease control?

11. What are the mechanisms for systemic acquired resistance to pathogens?

12. When a plant resists a pathogen, what stops the pathogen growing?

13. How do pathogens overcome plant disease resistance, and is it inevitable?

14. What are the molecular mechanisms for uptake and transport of nutrients?

15. Can we use non-host resistance to deliver more durable resistance in plants?

Most important questions relating to the understanding and utilization of plant cells:

1. How do plant cells maintain totipotency and how can we use this knowledge to improve tissue culture and regeneration?

2. How are growth and division of individual cells coordinated to form genetically programmed structures with specific shapes, sizes and compositions?

3. How do different genomes in the plant talk to one another to maintain the appropriate complement of organelles?

4. How and why did multicellularity evolve in plants?

5. How can we improve our understanding of programmed developmental gene regulation from a genome sequence?

6. How do plants integrate multiple environmental signals and respond?

7. How do plants store information on past environmental and developmental events?

8. To what extent do epigenetic changes affect heritable characteristics of plants?

9. Why are there millions of short RNAs in plants and what do they do?

10. What is the array of plant protein structures?

11. How do plant cells detect their location in the organism and develop accordingly?

12. How do plant cells restrict signaling and response to specific regions of the cell?

13. Is there a cell wall integrity surveillance system in plants?

14. How are plant cell walls assembled, and how are their strength and composition determined?

15. Can we usefully implant new synthetic biological modules in plants?

16. To what extent can plant biology become predictive?

17. What is the molecular/biochemical basis of heterosis?

18. How do we achieve high-frequency targeted homologous recombination in plants?

19. What factors control the frequency and distribution of genetic crossovers during meiosis?

20. How can we use our knowledge about photosynthesis and its optimization to better harness the energy of the sun?

21. Can we improve algae to better capture CO2and produce higher yields of oil or hydrogen for fuel?

22. How can we use our knowledge of carbon fixation at the biochemical, physiological and ecological levels to address the rising concentrations of atmospheric CO2?

23. What is the function of the phenomenal breadth of secondary metabolites?

24. How can we use plants as the chemical factories of the future?

25. How do we translate our knowledge of plant cell walls to produce food, fuel and fibre more efficiently and sustainably?

 Most important questions relating to plant diversity:

1. How much do we know about plant diversity?

2. How can we better exploit a more complete understanding of plant diversity?

3. Can we increase crop productivity without harming biodiversity?

4. Can we define objective criteria to determine when and where intensive or extensive farming practices are appropriate?

5. How do plants contribute to ecosystem services?

6. How can we ensure the long-term availability of genetic diversity within socio-economically valuable gene pools?

7. How do specific genetic differences result in the diverse phenotypes of different plant species? That is, why is an oak tree an oak tree and a wheat plant a wheat plant?

8. Which genomes should we sequence and how can we best extract meaning from the sequences?

9. What is the significance of variation in genome size?

10. What is the molecular and cellular basis of plants’ longevity and can plant life spans be manipulated?

11. Why is the range of life spans in the plant kingdom so much greater than in animals?

12. What is a plant species?

13. Why are some clades of plants more species-rich than others?

14. What is the answer to Darwin’s ‘abominable mystery’ of the rapid rise and diversification of angiosperms?

15. How has polyploidy contributed to the evolutionary success of flowering plants?

16. What are the closest fossil relatives of the flowering plants?

17. How do we best conserve phylogenetic diversity in order to maintain evolutionary potential?

Online Courses in Plant Genomics and Breeding from eXtension

The recently established website extention.org is a agricultural cooperative extention collective of 74 land grant universities which seeks to serve the public though education and service.

This fall there will be a plant breeding and genomics webinar series for plant breeders, breeding assistants, lab personnel, post docs, and graduate students.  These webinars will focus on how to use specific tools, such as software for genetics and mapping techniques, and on laboratory techniques across various topics of genomics and plant breeding.  For more information or to sign up to view a webinar go here or here.  Join the Plant Breeding and Genomics eXtension community of practice this fall for a webinar series to learn how to use tools, software, and techniques.

Potato Genome Sequence and Analysis

With next-generation sequencing technologies dropping in price and increasing in throughput, it’s not surprising to find multiple genomes published every week in scientific journals.  Most of these articles don’t qualify for publication in the top tier of journals like they did at the onset of the next-generation sequencing boom, but some genome sequencing projects, such as the potato genome, are high profile enough to warrant publication in top tier journals.

In the July 14th issue of the journal Nature, a draft of the potato (Solanum tuberosum) genome was described in a paper authored by the Potato Genome Sequencing Consortium – a huge group of researchers from 26 institutions.

The potato is the world’s fourth most consumed food crop, the most commonly grown vegetable crop, and a member of the economically important Solanaceae family –otherwise known as the nightshades – which include tomato, peppers, aubergine (eggplant if you live in the United States), tobacco, and petunia.  Widely distributed in western South America, tuber forming Solanum species are highly morphologically diverse and easily cross with other varieties for breeding purposes.

It’s been a bumpy road sequencing the potato genome since the project was started in 2006.  The potato genome is an extremely heterozygous autotetraploid, which translates to four highly variable copies of each of the 12 chromosomes.  It’s also the first sequenced Eudicot genome in the Asterid clade, so there are no close genetic relatives to provide the basis for a guided genome assembly.

The consortium began the sequencing by creating a bacterial artificial chromosome (BAC) library of 78,000 clones from a well studied diploid line providing high quality potatoes, named RH89-039-16.  The group used the BAC library and 10,000 AFLP markers to create more than 7000 contigs which were constructed into a physical map.  The group then identified up to 150 BACs for every chromosome on the potato genome, and verified their locations using fluorescent in situ hybridization.

Heterozygosity was so high in the RH line that after thorough sequencing the group hit an impasse with the assembly of the genome.  In an attempt to complement the sequencing of the RH line, the consortium began sequencing a doubled monoploid potato clone, DM1-3 516R44, derived from a diploid wild South America accession.  The DM line has a simpler genome than the RH line and is highly homozygous.

Using both the Illumina Genome Analyzer II and Roche 454 pyrosequencing platforms, and supplementing this data with traditional Sanger sequencing, approximately 96 Gb of data was acquired for the DM line.  The group then used the SOAPdenovo computer program to assemble the reads with a final assembly of 727 Mb for the DM line and a final estimation of 844 Mb for the genome.

The consortium generated more than 31 Gb of transcriptome data from both the DM and RH line libraries.  These 48 libraries represented major tissue types, developmental stages, and included various responses to abiotic and biotic stresses.  All the reads from the RNA-Seq libraries were mapped to the assembled DM genome.  Using gene prediction methods, along with protein and EST data, the potato genome was predicted to contain 39,000 protein coding genes, an amount which is in agreement with other plant genomes.  Within these genes, there were an estimated 2,642 asterid-specific and 3,372 potato-lineage-specific genes.  Some of the predicted asterid-specific genes include many novel transcription factors, self-incompatibility factors, and defence-related proteins. The draft assembly of the genome consists of more than 60% repeated elements.  The largest class of the transposable elements is the long terminal repeat retrotransposons (LTRs) which are estimated at 30% of the potato genome.

The potato is notorious for being susceptible to many pathogens and pests.  This well known susceptibility was one of the priorities for sequencing the genome and determining genes responsible for disease resistance and pathogen defense.  The DM genome assembly contains more than 800 putative R genes, responsible for conferring disease resistance, including 408 NBS-LRR-encoding genes, 57 Toll/interleukin-1 receptor (TIR) domains, and 351 non-TIR type resistance genes.  An extreme number of pseudogenes – attributed to indels, frameshift mutations, and misplaced stop codons –were identified within known R gene motifs, which possibly explains the potato’s inability to fight off some specific diseases.

One such well known disease, Late Blight, caused by Phytophthora infestans, was responsible for the Irish Potato Famine in the 1840s..  Using information from this genome sequencing project and other studies, we now know the variety brought to Europe in the late 16th century happens to lack specific disease resistance genes for Phytophthora infestans.  One could speculate that unbridled transposon jumping caused the inactivation of many R genes in this potato variety.

Unique for the potato is the formation of tubers (the actual potatoes) through the modification of a stolon.  The tomato is very closely related to potato, but does not produce stolons or modified tubers.  The group used transcript data from both potato and tomato to address genetic regulation of the formation of stolons and the transition of stolons to tubers.  Quite interestingly, the formation of stolons and tubers coincides with an up-regulation of genes associated with starch biosynthesis, protein storage, and Kunitz protease inhibitor genes associated with pests and pathogens.

Possibly due to extremely high levels of heterozygosity, it has been difficult to improve the potato through traditional breeding efforts.  It’s estimated that there is a worldwide economic loss of 4.5 billion US dollars to potato crops from diseases each year.  Just to attempt to suppress these diseases copious amounts of pesticides and fungicides are applied to potato crop land each year.  The potato cyst nematode, for example, is an important pest that researchers hope to improve resistance to via breeding initiatives.  Having this draft potato genome sequence will aid in the characterization of existing germplasm collections and description of allelic variance in breeding efforts to avoid diseases.  The potato genome will also serve as a resource for breeders wanting to improve the quality of other economically important Solanaceous plants such as tomato, pepper, eggplant, and tobacco.

Genome Sequence of the Date Palm

Published in the June 2011 issue of the journal Nature Biotechnology was a paper reporting on the genome sequence of the data palm, Phoenix dactylifera.  This paper, authored by Al-Dous et al., addressed the genome sequencing and de novo assembly of this agriculturally important monocot tree, along with comparative genomics with other plants.

Dates have been found in the tombs of pharaohs estimated at 8,000 years old.  Fields of agriculturally planted trees, estimated to be older than 5,000 years, suggest the date palm is one of the oldest cultivated plants in the world.  Dates are the most important agricultural crop in the hot and arid regions surrounding the Arabian Gulf and their global production is close to 7 million tons yearly.

Despite a prolonged emphasis on their agriculture, there are a few problems to deal with if you are a date grower.  Typical of tree crops, there is a long generation time from seedling to fruit harvesting.  Additionally, only the female date palm provides fruit and it takes at least 5 years after seed germination to tell if you have a male or female plant.  To make it even harder for a date grower, there are more than 2000 date varieties, each exhibiting its own color, flavor, size, shape, and ripening schedule, and they are all really hard to keep track of based on conventional techniques.

In an effort to provide genetic resources for date growers and breeders, the authors of this study – who were mainly located in Qutar – sequenced and assembled 380 Mb of the estimated 658 Mb genome of the Khalas cultivar, which is known for high fruit quality.  Generated using short reads from the Illumina Genome Analyzer IIx platform, this partial sequence excluded numerous large repeated regions, includes a predicted 28,890 genes, and represented 18 pairs of chromosomes.  The authors estimate that this draft genome represents roughly 90% of the total genes and 60% of the total genome.

This genome resource also serves a comparative genomics purpose by being the first member of the widespread monocot order Arecales.  To this date, the only Monocots with sequenced genomes – for example: Corn, Rice, and Sorghum – have all been in the grass order, the Poales.

This report is missing some vital information: in addition to an incomplete genome assembly, there is no metabolic, developmental, or gene network pathway reconstruction for the date palm provided in this paper (and unfortunately this paper also includes some glaring typos in the citation section).  In place of these expected analyses, the authors conducted a throughout survey of SNPs in this Khalas cultivar, along with eight additional cultivars common in breeding programs for the date palm.  Within these nine cultivars, 3,518,029 SNPs were determined, but quite interestingly, a total of 32 SNPs could be used to differentiate the cultivars.

In addition to the throughout SNP analysis, the researchers then did a full parentage analysis of the cultivars used in this study, which includes the famous date varieties such as Deglet Noor, Dayri, and Medjool.  Here‘s an article in Nature Middle East on the importance of understanding this parentage and gender analysis.

Although this is a draft genome still being completed and undergoing resequencing, namely the tools provided by the authors, the SNP and parentage analysis, should provide date palm breeders with many resources for improved fruit quality and this genome represents an exciting piece of the monocot evolutionary puzzle.