(Below N is a link to NCBI taxonomic web page and E link to ESTHER at designed phylum.) > cellular organisms: NE > Eukaryota: NE > Viridiplantae: NE > Streptophyta: NE > Streptophytina: NE > Embryophyta: NE > Bryophyta: NE > Bryophytina: NE > Bryopsida: NE > Funariidae: NE > Funariales: NE > Funariaceae: NE > Physcomitrella: NE > Physcomitrella patens: NE
LegendThis sequence has been compared to family alignement (MSA) red => minority aminoacid blue => majority aminoacid color intensity => conservation rate title => sequence position(MSA position)aminoacid rate Catalytic site Catalytic site in the MSA MRNAGSMPAISCGREIMLRSYLSTRPILPARFVLYSCLKTSSLIPLITPR RVSIPRRQLQLASVRSCSGKALVQDTPIEWTRNRSSVRLFATARDTGGKQ AIESEVESITGGDLGPIGKPEICTADELHYVAVPKTTWRLALWRYRPSKS APKRNHPVLMLSGIGTNAIGFDLDPSASLARHLAAAGFDSWILEVRGSGL SKREGEPTSSELGGTDGALNGAVQDAFVQATVKSATKAAEKKGNGAVAQE KNENPLKPQSNALAKVDKSSKEEDSVASRMTSRITQISQTLRSLVSEGQS RVSVANLLEQVTSLLEDKVLNERFENLRERLTALLEGPQTNSVASQVAEF SNSVTALLEEGQRSVTPSVTSLQERLTATITEFQEVLELIAKYDWDFDTY LQEDVPAAMEYVINHTGSPDGKVLGVGHSMGGILLYAMLAIREERAGLAG AVSLASSLDYAVSDTSLKMLLPLTDPAQRLNVPVVPLGALMTAIHPLSTR PPYALAYLGYQVSARSMMEPELFKKLVCNNFCTIPVKLLLQLATVFKPGG LQNRDGTVKYMERLHSCKVPVLAVAGDEDLICPPIAVSDTLKVFPQANVT YKLFGGEDDRHYGHYDLLCSRTAKREVYPVITDFLVKCDNTKVDSSG
The draft genome of the moss model, Physcomitrella patens, comprised approximately 2000 unordered scaffolds. In order to enable analyses of genome structure and evolution we generated a chromosome-scale genome assembly using genetic linkage as well as (end) sequencing of long DNA fragments. We find that 57% of the genome comprises transposable elements (TEs), some of which may be actively transposing during the life cycle. Unlike in flowering plant genomes, gene- and TE-rich regions show an overall even distribution along the chromosomes. However, the chromosomes are mono-centric with peaks of a class of Copia elements potentially coinciding with centromeres. Gene body methylation is evident in 5.7% of the protein-coding genes, typically coinciding with low GC and low expression. Some giant virus insertions are transcriptionally active and might protect gametes from viral infection via siRNA mediated silencing. Structure-based detection methods show that the genome evolved via two rounds of whole genome duplications (WGDs), apparently common in mosses but not in liverworts and hornworts. Several hundred genes are present in colinear regions conserved since the last common ancestor of plants. These syntenic regions are enriched for functions related to plant-specific cell growth and tissue organization. The P. patens genome lacks the TE-rich pericentromeric and gene-rich distal regions typical for most flowering plant genomes. More non-seed plant genomes are needed to unravel how plant genomes evolve, and to understand whether the P. patens genome structure is typical for mosses or bryophytes.
We report the draft genome sequence of the model moss Physcomitrella patens and compare its features with those of flowering plants, from which it is separated by more than 400 million years, and unicellular aquatic algae. This comparison reveals genomic changes concomitant with the evolutionary movement to land, including a general increase in gene family complexity; loss of genes associated with aquatic environments (e.g., flagellar arms); acquisition of genes for tolerating terrestrial stresses (e.g., variation in temperature and water availability); and the development of the auxin and abscisic acid signaling pathways for coordinating multicellular growth and dehydration response. The Physcomitrella genome provides a resource for phylogenetic inferences about gene function and for experimental analysis of plant processes through this plant's unique facility for reverse genetics.
Physcomitrella patens subsp. patens (Moss) PpKAI2-like H Predicted protein