Details

Autor(en) / Beteiligte

• Stevens, Kristian A
• Wegrzyn, Jill L
• Zimin, Aleksey
• Puiu, Daniela
• Crepeau, Marc
• Cardeno, Charis
• Paul, Robin
• Gonzalez-Ibeas, Daniel
• Koriabine, Maxim
• Holtz-Morris, Ann E
• Martínez-García, Pedro J
• Sezen, Uzay U
• Marçais, Guillaume
• Jermstad, Kathy
• McGuire, Patrick E
• Loopstra, Carol A
• Davis, John M
• Eckert, Andrew
• de Jong, Pieter
• Yorke, James A
• Salzberg, Steven L
• Neale, David B
• Langley, Charles H

Titel

Sequence of the Sugar Pine Megagenome

Ist Teil von

• Genetics (Austin), 2016-12, Vol.204 (4), p.1613-1626

Ort / Verlag

United States: Genetics Society of America

Erscheinungsjahr

2016

Link zum Volltext

Quelle

Electronic Journals Library

Beschreibungen/Notizen

• Until very recently, complete characterization of the megagenomes of conifers has remained elusive. The diploid genome of sugar pine (Pinus lambertiana Dougl.) has a highly repetitive, 31 billion bp genome. It is the largest genome sequenced and assembled to date, and the first from the subgenus Strobus, or white pines, a group that is notable for having the largest genomes among the pines. The genome represents a unique opportunity to investigate genome "obesity" in conifers and white pines. Comparative analysis of P. lambertiana and P. taeda L. reveals new insights on the conservation, age, and diversity of the highly abundant transposable elements, the primary factor determining genome size. Like most North American white pines, the principal pathogen of P. lambertiana is white pine blister rust (Cronartium ribicola J.C. Fischer ex Raben.). Identification of candidate genes for resistance to this pathogen is of great ecological importance. The genome sequence afforded us the opportunity to make substantial progress on locating the major dominant gene for simple resistance hypersensitive response, Cr1 We describe new markers and gene annotation that are both tightly linked to Cr1 in a mapping population, and associated with Cr1 in unrelated sugar pine individuals sampled throughout the species' range, creating a solid foundation for future mapping. This genomic variation and annotated candidate genes characterized in our study of the Cr1 region are resources for future marker-assisted breeding efforts as well as for investigations of fundamental mechanisms of invasive disease and evolutionary response.