The human brain has yet to explain the origin of one its defining features – the deep fissures¹（裂纹，龟裂） and convolutions（脑回，盘旋） that increase its surface area and allow for rational and abstract thoughts. An international collaboration² of scientists from the Yale School of Medicine and Turkey may have discovered humanity's beneficiary – a tiny variation within a single gene³ that determines the formation of brain convolutions – they report online May 15 in the journal Nature Genetics.

A genetic⁴ analysis of a Turkish patient whose brain lacks the characteristic convolutions in part of his cerebral⁵ cortex revealed that the deformity was caused by the deletion of two genetic letters from 3 billion in the human genetic alphabet. Similar variations of the same gene, called laminin gamma3 (LAMC3), were discovered in two other patients with similar abnormalities.

"The demonstration⁶ of the fundamental role of this gene in human brain development affords us a step closer to solve the mystery of the crown jewel of creation, the cerebral cortex," said Murat Gunel, senior author of the paper and the Nixdorff-German Professor of Neurosurgery, co-director of the Neurogenetics Program and professor of genetics and neurobiology at Yale.

The folding of the brain is seen only in mammals with larger brains, such as dolphins and apes, and is most pronounced in humans. These fissures expand the surface area of the cerebral cortex and allow for complex thought and reasoning without taking up more space in the skull⁷. Such foldings aren't seen in mammals such as rodents⁸（啮齿类） or other animals. Despite the importance of these foldings, no one has been able to explain how the brain manages to create them. The LAMC3 gene – involved in cell adhesion（粘附，支持） that plays a key role in embryonic⁹ development – may be crucial to the process.

An analysis of the gene shows that it is expressed during the embryonic period that is vital to the formation of dendrites（树突） , which form synapses¹⁰ or connections between brain cells. "Although the same gene is present in lower organisms with smooth brains such as mice, somehow over time, it has evolved to gain novel functions that are fundamental for human occipital cortex formation and its mutation¹¹ leads to the loss of surface convolutions, a hallmark of the human brain," Gunel said.